Thermostable xylanases

TECHNICAL FIELD
The present invention relates to novel microorganisms and to novel enzymes. More specifically, the enzymes are thermostable xylanases. These xylanases are obtainable from anaerobic thermophilic bacteria. The xylanases are applicable under conditions used in the paper and pulp industry i.e. a pH of above 9 and a temperature of above 70.degree. C., specifically the enzymes are active at T=80.degree. C.
BACKGROUND OF THE INVENTION
Xylan is a component of plant hemicellulose. Xylan consists of a backbone of 1,4-glycosidically linked .beta.-D-xylose. Usually xylans have side chains or groups comprising xylose and other pentoses, hexoses, uronic acids and acetyl groups.
In the paper production process the bleaching of pulp is an important step. Schematically, the process used for pulp treatment in the paper and pulp industry is performed as follows: Pulp is treated at pH 10-12 at 80.degree. C. to remove most of the lignin in the so-called oxygen delignification step. The remaining pulp contains 2-5% of lignin. This lignin gives the pulp its brown color. Subsequently, the pulp is bleached in a multistage bleaching process. In this bleaching process chemicals such as chlorine, chlorine dioxide, hydrogen peroxide and/or ozone are used, to obtain a bright pulp for high quality paper.
Chlorine and chlorine-containing chemicals are often used in the bleaching process. However, since the use of these chemicals leads to the formation of dioxin and other chlorinated organic compounds, they form a threat to the environment. Therefore, there is a growing tendency to omit the use of chemicals giving rise to this kind of waste products.
This has prompted a tendency to develop chlorine-free processes; total chlorine-free (TCF) and elementary chlorine-free (ECF). In these processes hydrogen peroxide or ozone is used for bleaching. However, the use of these oxidative chemicals may have a negative effect on the quality of the paper, especially the strength of the paper
It has been found that certain enzymes make the pulp more accessible to bleaching agents, thereby reducing the amount of bleach. Xylanases, in particular, have been found to be very useful in the paper and pulp processing. Xylanases have been reported to increase the extractability of lignins from the pulp. In current processes, xylanases are mostly used after the oxygen delignification step, because they are not active and do not survive under conditions used during oxygen delignification.
Xylanases cleave the hemicellulose chains which are responsible for the close adherence of lignin to the cellulose network. After xylanase treatment the lignin is more easily removed in the subsequent steps.
Therefore the use of xylanases leads to a reduction of the consumption of active chlorine in prebleaching of 25-30%. This reduction of chlorine does not afflict the quality parameters of the resulting paper (Viikari et al. 1986. Proc. of the third Int. Conf. Biotechnology in Pulp and Paper Ind., Stockholm, p.67-69 and Bajpai and Bajpai. 1992. Process Biochemistry. 27:319-325).
The xylanase treatment also reduces the need for other chemicals, such as hydrogen peroxide, in the bleaching process.
The use of xylanases from fungal sources in bleaching of kraft pulp has been reported. These are acidic xylanases and the pH and temperature optima of the enzymes are: pH 3-5 and T 30-50.degree. C. These values are not ideal for the use in the bleaching process, where the prevailing conditions; are pH.gtoreq.9 and temperature .gtoreq.70.degree. C.
Xylanases from bacterial origin, with higher pH and/or temperature optima, have been reported for use in the bleaching process. Some of these originate from the following species (pH and temperature optima of the reported xylanase activity between brackets):
Bacillus pumilus (pH=7-9, T =40.degree. C., Nissen et al. 1992. Progress in Biotechnology 7:325-337), Bacillus stearothermoohilus (pH=7, T=65.degree. C. International patent application WO 91/10724), Dictyoglomus thermophiluim (pH=6-8, T=70.degree. C., European patent application EP 0 511 933), Rhodothermus (pH=5.5-6.5, T=80-100.degree. C., European patent application EP 0 538 177), Thermotoga (pH=5-6, T=90.degree. C., International patent application WO 93/19171) and Thermoanaerobacter ethanolicus (T=68.degree. C., Deblois and Wiegel. 1992. Progress in Biotechnology 7:487-490).
Although the use of some of these xylanases for bleaching has been claimed, no xylanases have been reported to date having the desired characteristics of significant delignification activity at temperature .gtoreq.80.degree. C.
SUMMARY OF THE INVENTION
The present invention discloses xylanases obtainable from anaerobic thermophilic microorganisms which have been isolated in pure culture from hot springs in New Zealand. The microorganisms have been deposited at the Centraal Bureau voor Schimmelcultures (CBS), Baarn, the Netherlands, on Apr. 14, 1994.
The present invention also discloses enzymes having substantial xylanase activity at a temperature of at least 80.degree. C. Furthermore, the present invention discloses that said xylanases possess significant delignification activity at a temperature of at least 80.degree. C. Said enzymes are obtainable from the deposited strains.
The present invention further describes a process for the preparation of the xylanases which are active at a temperature of 80.degree. C. The process comprises cultivation of the deposited microorganisms of the present invention in a suitable medium, followed by recovery of the enzymes having the indicated activity.
The present invention also discloses the cloning of the genes encoding the subject xylanases. Expression of these genes in a host cell is also disclosed. The enzymes are essentially pure when obtained in this manner.
Thus the present invention also discloses another method for obtaining the xylanases, i.e. expression of recombinant DNA. The present invention further describes the application of the xylanases under conditions equivalent to industrial application conditions, using high temperature and high pH.

BRIEF DESCRIPTION OF THE FIGURES
FIG. 1: Phylogenetic analysis of the internal consensus sequences of the six extremophilic strains. Sequences are named as followed; organism/forward primer/recombinant number. The branch number displayed are the values obtained from a boot-strap analysis of the sequences.
FIG. 2: Sequence alignment of- family G internal consensus sequences.
FIG. 3: The xylanase domain of xynD from-TG456 inserted as a Sphl-BamHl fragment in pJLA602.
FIGS. 4A-4D: Paper properties of paper prepared from hardwood pulp TCF bleached as described in Example 15. Ref=no enzyme, 715=TG456 xynD, 716=Tg53 xynD. Tensile index (A), porosity (B), tear (C) and burst (D) in relation to Schoppen-Riegler values are given.
FIGS. 5A-5D: Paper properties of paper prepared from hardwood pulp ECF bleached as described in Example 15. Ref=no enzyme, 715=TG456 xynD, 716=Tg53 xynD. Tensile index (A), porosity (B), tear (C) and burst (D) in relation to Schoppen-Riegler values are given.
FIGS. 6A-6D: Paper properties of paper prepared from softwood pulp TCF bleached as described in Example 15. Ref=no enzyme, 715=TG456 xynD, 716=Tg53 xynd. Tensile index (A), porosity (B), tear (C) and burst (D) in relation to Schoppen-Riegler values are given.
FIGS. 7A-7D: Paper properties of paper prepared from softwood pulp ECF bleached as described in Example 15. Ref no enzyme, 715=TG456 xynD, 716=Tg53 xynD. Tensile index (A), porosity (B), tear (C) and burst (D) in relation to Schoppen-Riegler values are given.
FIGS. 8A-8D: Refining curves as determined in Example 15 for TCF (A) and ECF (B) bleached hardwood pulp and for TCF (C) and ECF (D) bleached softwood pulp. Ref=no enzyme, 715=TG456 xynD, 716=Tg53 xynD.
FIGS. 9A-9B: A comparison of the pH optima (A) and temperature optima (B) of the TG456 xynD xylanase and Pulpzyme HB (Novo Nordisk).
FIGS. 10A-10B: A comparison of the thermostabilities of the TG456 xynD xylanase and Pulpzyme HB (Novo Nordisk) at 80.degree. C., pH 7.0 (A) and at 65.degree. C.; pH 9.0 (B).

DETAILED DESCRIPTION OF THE INVENTION
The present invention discloses microorganisms which have been isolated from hot springs in New Zealand. These microorganisms have been characterized as anaerobic thermophilic bacteria and have been classified according to Rainey (1992. PhD thesis, University of Waikato, Hamilton, New Zealand).
The microorganisms have subsequently been screened using a xylan-agar diffusion assay. Strains which showed a clearing zone in this test were selected as potential xylanase producing strains. The strains were grown under anaerobic conditions at pH 7-0 and T=75 or 80.degree. C. depending on the organism. After concentration by ultrafiltration, the culture broth was analyzed for xylanase activity in an assay at pH=6.5 and 9 and T=80.degree. C. (Example 1).
Six different strains were found to produce xylanase activity under the indicated conditions. These microorganisms have been deposited at the CBS (Centraalbureau voor Schimmelcultures) on Apr. 14, 1994 under deposition numbers: CBS 211.94, CBS 212.94, CBS 213.94, CBS 214.94, CBS 215.94 and CBS 216.94 These deposits were made in conformity with the Budapest Treaty, and will become irrevocably available to the public upon the granting of the patent herein.
The present invention also discloses enzymes having xylanase activity, specifically enzymes having at least a considerable xylanase activity at a temperature of at least 80.degree. C. and a pH of 6 or higher. Said enzymes are obtainable from the deposited strains. Said enzymes are also obtainable from mutants and variants of the deposited strains.
With the expression "considerable activity" is meant that the enzymes of the present invention have at least 80.degree. C., at least 40% of the activity they possess at 70.degree. C., preferably this is at least 60%, more preferably about at least 80%, even more preferably about 200%.
The present invention further describes a process for the preparation of the xylanases which are active at a temperature of about 80.degree. C. or having a considerable activity under these conditions. The process comprises cultivation of the deposited microorganisms of the present invention in a suitable medium, followed by recovery of the enzymes having the indicated activity. Isolation and purification of the xylanase can be performed using standard procedures known in the art.
A partial purification of the enzymes is exemplified in Example 2. In this example the cells are first removed by hollow fibre filtration. Subsequently, the protein is further purified by ammonium sulphate addition to a final concentration of 1M. The solution is then brought on a phenyl sepharose column and the protein eluted with 1M NaCl. Finally, the protein is concentrated by ultrafiltration and salt is removed by diafiltration.
To establish the xylan degrading potential of the xylanases at an alkaline pH, a comparison of the activities of the xylanases isolated from the indicated strains at a pH of 7 and 9 has been made using different substrates and a temperature of 70.degree. C. (Example 3). The xylanases have been shown to possess considerable activity at alkaline pH. Depending on the substrate and the assay, at pH 9 the xylanases have about 20% or more of the activity they possess at pH 7. One xylanase was shown to retain 80% of its pH 7 activity at pH 9.
The thermostability of the xylanases isolated from the indicated strains varies considerably. Some of the xylanases are very thermostable they have a half-life of more than 2 hours at pH=9 and at 80.degree. C. (see Example 4), The half-life at pH=9.0 and 80.degree. C. of the xylanases of the invention is at least 10 minutes, preferably the half-life under these conditions is more than 20 minutes, more preferably it is more than 30 minutes, still more preferably it is more than 60 minutes and most preferably the half-life is more than 120 minutes.
The present invention also discloses the cloning and expression of a DNA sequence characterized in that it encodes a xylanase obtainable from an anaerobic thermophilic strain. The invention discloses vectors, which include expression vectors, characterized in that they contain the DNA sequence encoding the xylanases of the present invention. A microbial host cell characterized in that it is transformed with one of these vectors is also disclosed.
Sequence analysis of the DNA sequences encoding the xylanases of the invention revealed that the obtained sequences fall into two groups of enzymes families, i.e. the F-type and G-type xylanases as previously defined by Gilkes et al. (1991, Microbiol. Rev. 55: 303-315). The xynA, xynB and xynC sequences obtained from the microorganisms of the invention belong to the F-type xylanases; the xynD sequences obtained from these microorganisms belong to the G-type xylanases (see examples 6,7,8 and 9). G-type xylanases from thermophilic microorganisms have not been described previously to the best of our knowledge. The thermophilic microorganisms which are the source of the xylanases of the invention are herein defined as microorganisms with an optimum growth temperature which is higher than 65.degree. C. Preferably the optimum growth temperature is higher than 68.degree. C., more preferably the optimum growth temperature is higher than 70.degree. C., and most preferably the optimum growth temperature is in excess of 75.degree. C.
Expression of the both F-type and G-type xylanase DNA sequences of the invention in E.coli is shown to give an active proteins (see Example 10 and 11). Said proteins are active at a temperature of 80.degree. C.
The cloning and expression demonstrated in the examples of the present description makes possible expression of the genes in homologous organisms. Expression can also be performed in other microorganism using suitable expression and secretion regulating sequences. Organisms of choice are yeast, fungi and bacteria. Specific micro-organisms include strains selected from Aspergillus niaer, Kluyveromyces lactis and Bacillus licheniformis.
The enzymes of the present invention have been shown to possess a considerable activity on oat spelts xylan and on birchwood xylan.
The enzymes of the present invention have further been tested for their bleaching capacity. This bleaching capacity is determined by the delignifying activity of the enzymes of the present invention. The invention discloses enzymes which have a significant delignifying activity, as measured on several wood pulps. The enzyme preparations, xylanases, are capable of delignifying wood pulp at a temperature of at least 80.degree. C. The expression "wood pulp" is to be interpreted broadly and is intended to comprise all kinds of lignocellulosic materials.
The enzymes have been tested for their bleaching capacity on both hardwood and softwood pulps. Lignin removal has been measured according to two different methods (Example 5). Lignin in the medium was determined by the A300 test. In this test all preparations showed significant delignifying activity at 80.degree. C. on both hard- and softwood. At pH 9 and 80.degree. C. the activity on softwood was at leas. 43% of the activity at pH 6, while on hardwood 3 strains showed at pH 9 activities of more than 50% as compared to pH 6, and 3 others 18-30%. Bleaching of softwood pulp was also measured by determining the decrease in the lignin content of the pulp using the kappa test. The kappa number was decreased 0.5 to 14 units after incubation of the pulp at pH 9 and 80.degree. C. with the xylanase preparations.
Additionally, the bleaching capacity of the enzymes of the present invention can be measured by e.g. the increase of ISO brightness of paper produced with conventionally treated pulp, additionally incubated with said enzymes, as compared to incubation without enzymes. Said conventional treatment comprises exposition to bleaching agents such as H.sub.2 O.sub.2, ozone, Cl.sub.2 or ClO.sub.2, according to the art.
The cloned F-type and G-type xylanases of the invention as expressed in E.coli have also been tested for their performance in ECF bleaching experiments on both softwood and hardwood pulp (see Example 12). Surprisingly, we have observed that the G-type xylanases (encoded by the xynD genes) show a much better performance in bleaching sequences on both softwood and hardwood pulp as compared to the F-type xylanases, up to 6.8% ISO delta brightness over the no-enzyme control, which compares to at most 1.2% ISO brightness increase for the best F-type xylanase. Further testing of the thermostable G-type xylanases showed that they also produce excellent results in TCF bleaching experiments on both softwood and hardwood pulp (see Examples 14 and 15). Verification of the properties of the paper produced from the thus bleached pulp showed no significant differences with the no-enzyme control paper.
The cloned G-type xylanases are highly thermostable, even at high pH. A half-life at 80.degree. C. and pH 7.0 of more than 30 minutes was measured. At 65.degree. C. and pH 9.0 the half-life of the enzyme is not significantly reduced, even after 120 minutes of incubation (see Example 16). The half-life at pH 9.0 and 65.degree. C. of the G-type xylanases of the invention is at least 10 minutes, preferably the half-life under these conditions is more than 20 minutes, more preferably it is more than 30 minutes, still more preferably it is more than 60 minutes and most preferably the half-life is more than 120 minutes.
The invention discloses DNA sequences encoding thermostable G-type xylanases the internal consensus fragment (ICF) of which shows more than 80% identity with the ICF of SEQ ID NO 12. The G-type ICF is herein defined as the fragment which lies in between the sequences corresponding to SEQ ID NO 4 and SEQ ID NO 5 in SEC ID NO 12 (nucleotide positions 295 to 623). Preferably the identity with the G-type ICF is more than 87%, more preferably the identity is more than 95%, most preferably, the identity is more than 99%.
In a further embodiment, the invention discloses G-type xylanase sequences which share at least 70% identity with the amino acid sequence of SEQ ID NO 13. Preferably this amino acid identity is-more than 80%: more preferably, the amino acid identity is more than 90%; still more-preferably the amino acid identity is more than 95%; most preferably the amino acid identity is more than 99%.
The enzymes of the present invention can be used immediately after the oxygen delignification step in the pulp preparation process described above. As a consequence of the temperature and pH characteristics of the enzymes, extensive cooling and pH adaptation can be avoided. In another embodiment of the invention, the enzymes are used before or during the oxygen delignification step. Before this step the lignin concentration is much higher and therefore the effect of the application of the xylanase is much larger.
Furthermore, applications of the enzyme preparations of the present invention are described, particularly a process in which wood pulp is treated with said enzyme preparations according to the invention.
Similarly, a fluff pulp can be treated with the enzyme preparations according to the invention.
The invention further relates to paper, board and fluff pulp made from a wood pulp treated with the enzyme preparations according to the invention.
EXAMPLE 1
Isolation of strains producing thermostable xylanase activity
Xylanase-producing microorganisms were obtained from hot-springs in various thermal areas of New Zealand. The strains were isolated by in situ enrichment using oat spelts xylan as substrate from hot springs having a temperature of above 70.degree. C., and a pH between 6.0 and 8.5. Cultures of strains were obtained by further anaerobic cultivation in the laboratory on 2/1 medium plus xylan at a temperature (70.degree., 75.degree. or 85.degree. C.) corresponding to the temperature of the site from which the sample was taken.
The composition of the 211 medium plus xylan is as follows:
______________________________________ Anaerobic 2/1 medium Resazurin (0.1%) 1.0 ml/l SL10 Trace Elements 1.0 ml/l FeCl.sub.3 soln. (0.28 mg/ml) 1.0 ml/l Wolin's Vitamins 0.1 ml/l NaCl 0.9 g/l MgCl.sub.2.6H.sub.2 O 0.2 g/l K.sub.2 HPO.sub.4 1.5 g/l KH.sub.2 PO.sub.4 0.75 g/ NH.sub.4 Cl 0.9 g/l Cysteine 0.75 g/l Yeast Extract 0.5 g/l Bacto Tryptone 1.0 g/l Oat spelts xyian 2 g/l pH 7.0 Dispense under N.sub.2 gas Wolin's Vitamin Mixture mg/100 ml Biotin 2.0 Folic acid 2.0 Pyridoxine HCl 10.0 Riboflavin 5.0 Thiamine 5.0 Nicotinic acid 5.0 Pantothenic acid 5.0 Vitamin B12 0.1 p-Aminobenzoic acid 5.0 Thioctic acid 5.0 SL10 Trace Elements modified 5M HCL 15 ml mg/l ZnCl.sub.2 70 MnCl.sub.2.4H.sub.2 O 100 H.sub.3 BO.sub.3 6 CoCl.sub.2.6H.sub.2 O 130 CuCl.sub.2.2H.sub.2 O 2 NiCl.sub.2.2H.sub.2 O 24 NaMoO.sub.4. 2H.sub.2 O 36______________________________________
Pure cultures of strains were obtained from single colonies in agar roll tubes. Culture concentrates obtained by ultrafiltration were tested for xylanase activity at 70.degree. and 80.degree. C. and, at pH 6.5 and 9.0 using a dyed xylan method (see below) and the PAHBAH method (see Example 3).
Six strains which were deposited at the CBS (Centraal Bureau voor Schimmelcultures) are depicted in Table 1.
TABLE 1
______________________________________deposition numbers of strains used in this patent application strain CBS accession number______________________________________ TG 53 CBS 211.94 TG 453 CBS 212.94 TG 456 CBS 213.94 TG 457 CBS 214.94 TG 479 CBS 215.94 TG 631 CBS 216.94______________________________________
Dyed xylan, composed of larchwood xylan coupled to Remazol Brilliant Blue R (Sigma), was prepared following a method described by Biely et al (1985) Anal. Biochem 144, 142-146. Larchwood xylan (6.7 g) was placed into 250 ml water and stirred for several hours at room temperature to dissolve. Remazol Brilliant Blue R (10.0 g) was added to this mixture. After dissolving, 20 ml of a Na-acetate solution (2.7 g Na-acetate in 20 ml distilled water) was added dropwise. Then a solution of 6 g NaCH in 70 ml water was added and stirring continued for 18 hours. The dyed xylan which had formed was precipitated by the addition of 700 ml 96% ethanol. After allowing to stand for 6 hours the precipitate was separated by filtration (Whatman GF/A). The filter cake was washed with 3 l of a 2:1 mixture of 96% ethanol/0.05M Na-acetate, followed by 1 I-96% ethanol and 3 l acetone until the filtrate was colorless. The yield was 10.5 g dyed xylan.
For the enzyme assay, 5.1 g dyed xylan was dissolved in 150 ml 0.1M MOPS buffer, pH 6.8. The mixture was stirred at 70.degree. C. for 4 hours to dissolve. After cooling to room temperature insoluble material was removed by centrifugation at 10,000 x g. For activity assays, the stock solution containing 3.34% w/v dyed xylan was diluted with 0.1M MOPS buffer, pH 6.8 to give a 0.5% dyed xylan working solution.
The enzyme assay using dyed xylan was performed by adding 0.9 ml dyed xylan solution (0.5%) to 0.6. ml enzyme preparation in an appropriate buffer with mixing. A portion (0.4 ml) of this mixture was transferred into 0.8 ml 96% ethanol as control (blank). The remaining solution was incubated at 70.degree. C. for 90 minutes. The reaction was terminated by transferring 0.4 ml of the test mixture into 0.8 ml 96% ethanol. This solution was left at room temperature for 30 minutes to allow for the precipitation of uncleaved dyed xylan. The test samples were centrifuged at for 5 minutes at full speed in a Beckman Microfuge E, and the absorbance of the supernatant was measured at 595 nm in a spectrophotometer.
EXAMPLE 2
Isolation of enzyme preparations
Anaerobic fermentations were carried out in 2 l Schott bottles containing 1800 ml of 2/1 plus xylan medium in stationary incubation at a temperature of either 75 or 80.degree. C. (depending on the organism being cultured) for 24 hrs. From 10 l of well-grown culture the cells were removed by hollow fibre filtration in the presence of 0.01% triton X100 (Amicon DC 10 LA and Amicon 0.1 .mu.m H5MP01-43 filter). Ammonium sulphate was added to the cell free culture medium to a final concentration of 1M. The resulting solution was pumped onto a 9.times.15 cm column containing 1 l of phenyl sepharose (Pharmacia-Fast Flow-low substitution) equilibrated with 1M ammonium sulphate. The flow rate was 150-200 ml/minute. The column was washed with 5 l 1M ammonium sulphate. The xylanase was eluted with 5 l 1M NaCl. Fractions were collected in 500-1000 ml volumes. The xylanase activity was determined (with the PAHBAH method as described in Example 3) in the fractions and the active fractions were pooled, ultrafiltered to a small volume and diafiltered to reduce the salt concentration using an Amicon Stirred Cell (Model 2000A or 8400) with an YM2 membrane.
EXAMPLE 3
Characterization of xylanase activities of the partially purified enzyme preparations
Analytical methods
Assays for xylanase activity were performed using modified procedures of the Sumner assay (Sumner et al. 1921. J. Biol. Chem. 47: 5-9). Alternatively xylanase activity was determined using a modified PAHBAH assay, based on a method from Lever (1973. Biol. Med. 1: 274-281).
Procedure 1
Sumner assay of xylanase activity on oat spelts xylan
An oat spelts xylan substrate solution is prepared as follows: 4 g oat spelts xylan is suspended in 100 ml demineralized water. The suspension is sonicated for 6 minutes (sonicator: Sonics & Materials, Vibracell type VC 250 B), incubated at 100.degree. C. for 10 min., and centrifuged for 10 min. at 10,000 rpm in a Sorvall RC-5B centrifuge. The supernatant is used as a substrate solution and contains about 2% oat spelts xylan.
The assay is carried out as follows: A test tube is filled with 200 .mu.l oat spelts xylan solution, 600 .mu.l aliquots of enzyme preparation (Example 2) diluted in the appropriate buffer. The test tube is incubated under measuring conditions in a waterbath for 15 minutes. After the incubation, 7.2 ml DNS (dinitrosalicylic acid) reagent is added. The mixture is heated in a waterbath at 100.degree. C. for 10 minutes, whereafter the test tube is cooled on ice. The absorbance is measured at 575 nm. To eliminate the background absorbance of the enzyme samples a control experiment is executed as follows: a tube containing substrate without enzyme preparation is incubated under the same conditions as the test samples. After the 15 minutes incubation 7.2. ml. DNS and the enzyme sample is added (in this order).
One unit of xylanase (xU) activity is defined as the amount of enzyme producing 1 .mu.mol of xylose-equivalent,.measured as reducing-sugar.
Actual measuring conditions were pH 7.0,. 9.0 and 70.degree. C. At pH-7 a 50 mM phosphate buffer was used, and at pH 9 a 50 mN borate/KOH buffer.
TABLE 2______________________________________relative xyllanase activities on oat spelts xylan, measured at 70.degree. Activity (%)Strain pH 7.0 pH 9.0______________________________________TG 453 100 57 TG 456 100 39 TG 457 100 31 TG 479 100 19 TG 631 100 31______________________________________
Procedure 2
Sumner assay of xylanase activity on Birchwood xylan
Essentially the same method as described in procedure 1 is used. Instead of an oat spelts xylan solution a birchwood xylan suspension is used. A birchwood xylan substrate solution is prepared as follows: 4 g birchwood xylan is suspended in 50 ml 0.2N NaOH and agitated until visibly dissolved. The pH of the solution is adjusted to 7.0 with glacial acetic acid, water is added to 100 ml and the solution is centrifuged at 10,000 rpm in a Sorvall RC-5B centrifuge. The supernatant is used as a substrate solution and contains about 3% birchwood xylan. The test conditions were pH 7 and 9 and 70.degree. C. The results are shown in Table 3.
TABLE 3______________________________________relative xylanase activities on birchwood xylan, measured at 70.degree.C. Activity (%)Strain pH 7.0 pH 9.0______________________________________ TG 453 100 40 TG 456 100 20 TG 457 100 21 TG 479 100 12 TG 631 100 21______________________________________
Procedure 3
PAHBAH assay of xylanase activity on oat spelts xylan
The modification of the PAHBAH method (Lever, 1973) is to the PAHBAH reagent, as follows: 0.05M trisodium citrate, 0.1M Na.sub.2 SO.sub.3, 0.02M CaCl.sub.2, 0.5M NaOH and 0.1M p-hydroxybenzoic acid hydrazide (PAHBAH).
For the assay of the enzyme preparations 0.05 ml or 0.1 ml of enzyme preparation is mixed with 0.3 ml substrate buffer (50 mM Bis-Tris-Propane, pH as required, +0.2% oat spelts xylan in suspension). An appropriate amount of water is added to a final volume of 0.5 ml. Incubation is usually made at 70.degree. C. for 30 min. To stop the reaction, 1.0 ml of PAHBAH reagent is added after incubation and the samples are heated at 100.degree. C. for 6 minutes. The blanks consist of substrate buffer incubated identically to the sample to which the enzyme is added after the PAHBAH reagent. Before determination of the absorption at 420 nm, all samples are centrifuged 1 min at full speed in a Beckman Microfuge E to remove suspended xylan from the supernatant. The results are shown in Table 4. From this Table it can be concluded that at pH 9.0, 80.degree. C. all strains still have a considerable activity as compared with pH 6.0, 70.degree. C.
TABLE 4______________________________________relative xylanase activities on oat spelts xylan, measured with the PAHBAH assay Activity (%)Strain pH 6.0, 70.degree. C. pH 9.0, 80.degree. C.______________________________________ TG 53 100 57 TG 453 100 20 TG 456 100 65 TG 457 100 82 TG 479 100 30 TG 631 100 65______________________________________
EXAMPLE 4
Thermostability of xylanase activities
The half-life of the xylanase activity of the enzyme preparations was determined as follows. The enzyme preparation was diluted 1/10 in 100 mM TAPS buffer (pH 9.0 at 80.degree. C.) and incubated at 80.degree. C. A sample was removed at 0, 10, 20, 40, 60 and 120 minutes and added to 100 mM MOPS buffer (pH 6.0 at 70.degree. C.) on ice, to a final dilution of 1/20 to 1/100 as appropriate for the final assay. The samples were kept on ice until they were assayed at 70.degree. C. and pH 6.0 using the PAHBAH assay method as described in Example 3, procedure 3. The results are shown in Table 5.
TABLE 5______________________________________thermostability of xylanase activity at pH 9.0 and 80.degree. C., as measured with the PAHBAH assay on oat spelts xylan Half-life Strain pH 9.0, 80.degree.______________________________________ C.TG 53 30 minutes TG 453 60 minutes TG 456 >120 minutes TG 457 >120 minutes TG 479 <10 minutes TG 631 <20 minutes______________________________________
EXAMPLE 5
Delignification activities
Delignification capacity of the xylanases was determined with two different methods. Using the A300 method the amount of lignin released from the pulp after enzyme treatment is estimated. Using the kappa assay the remaining lignin content of pulp after treatment is measured.
Method 1: A300 test
To measure delignification with the A300 assay enzyme preparations were incubated with soft- or hardwood pulp at a concentration of 2 PAHBAH units per g of wet pulp (about 6 PAHBAH units/g of dry pulp). Incubations were performed for 2 hours at 80.degree. C. both at pH 6.0 in MOPS buffer, and at pH 9.0 in TAPS buffer. Pulp concentration in the incubation was 0.1 g wet weight per ml. Two different types of pulp were used: Kraft softwood pulp after oxygen delignification, and Kraft hardwood pulp after oxygen delignification. Properties of these pulps are given in Table 6.
TABLE 6______________________________________properties of the pulp types used in the delignification experiments Softwood Hardwood 80% spruce, 20% birch pine______________________________________ Brightness, % ISO 50.8 35.8 Kappa number 11.0 16.7 Viscosity, dm.sup.3 /kg 979 1003 Calcium; ppm 1900 2600 Copper, ppm 0.3 0.6 Iron, ppm 5.1 11 Magnesium, ppm 210 270 Manganese, ppm 25 70______________________________________
The amount of lignin that was removed from the pulp was determined by measuring the absorbance of the supernatant at 300 nm, after separating the supernatant from the pulp by filtration by suction through a Whatman GF/C filter supported on a sintered glass filter. The results of the A300-test are shown in Table 7. In this assay, Delta A300 values of .gtoreq.0.2 are significantly higher than background levels. Therefore, this example shows that the enzymes possess a significant delignifying activity at 80.degree. C.
TABLE 7______________________________________A300 delignification measured at 80.degree. C., pH 6.0 and 9.0, on soft- and hardwood Delta A300 Hardwood SoftwoodStrain pH 6.0 pH 9.0 %* pH 6.0 pH 9.0 %*______________________________________ TG 53 0.7 0.5 71 0.6 0.35 58 TG 453 1.0 0.3 30 0.7 0.3 43 TG 456 1.0 0.3 30 0.6 0.6 100 TG 457 1.0 0.7 70 1.0 0.5 50 TG 479 0.9 0.16 18 0.8 0.6 75 TG 631 1.2 0.7 58 0.8 0.7 88______________________________________ *Percentage of the activity at pH 9 as compared to pH 6
Method 2: the Kappa test
The kappa tests were performed according to TAPPI protocol T236 (available from TAPPI, Technology Park, Atlanta, USA), with some modifications. The enzyme preparation was added at a dose of 10 xU/g pulp (dry weight), and incubated for 2 hours at pH 9, 80.degree. C. As a control pulp was incubated for the same period under the same conditions without enzyme addition. Oxygen delignified softwood pulp was used, for properties see Table 6.
The difference between the kappanumber with enzyme addition and the kappanumber without enzyme addition is called the kappa reduction, and is a value for delignification. The kappa reductions are shown in Table 8. In this assay, values of .gtoreq.0.5 are significantly higher than background levels. Therefore, as in the previous example, this example shows that the enzymes possess a significant delignifying activity at 80.degree. C.
TABLE 8______________________________________delignification as measured by kappa reduction, determined on softwood pulp, pH 9 and 80.degree. C. Strain Kappa reduction______________________________________ TG 453 1.0 TG 456 1.3 TG 457 1.4 TG 479 1.0 TG 631 0.5______________________________________
EXAMPLE 6
Cloning and sequence determination of internal consensus fragments of genes encoding thermostable F-type xylanases
6.1. PCR amplification of internal fragments of xylanase genes
Three PCR primers were used to amplify internal consensus fragments of xylanase genes: two different forward primers (xynFA, {5' CAC ACK CTK GTK TGG CA 3', SEQ ID NO 1} and xynFB {5' CAT ACK TTK GTT TGG CA 3', SEQ ID NO 2) and one reverse primer (xynR {TMG TTK ACM ACR TCC CA, SEQ ID NO 3}). The xynFA and xynFB primers bound at the same location, but differed slightly in sequence due to slight differences in the sequence of xylanase genes at the forward consensus region. PCR conditions were as follows: (94.degree. C. 1 minute, 50.degree. C. 1 minute, 72.degree. C. 1 minute).times.30. All family F internal consensus fragments were approximately 350 bp.
6.2. Sequence determination of the PCR products
All internal xylanase PCR-products (ca. 350bp) were end-repaired (back-filled) as described below prior to cloning into the Smal (phosphatased) site of the M13 mp 10 sequencing vector.
Step 1--Ammonium acetate precipitation
(a) make up 50 .mu.l PCR mixture to 100 .mu.l with TE buffer (10 mM
Tris-Cl, 1 mM EDTA, pH 8.0). (b) add 100 .mu.I 4M CH.sub.3 COO-NH.sub.4.sup.+ and 250 .mu.l 100% CH.sub.3 CH.sub.2 OH. (c) incubate on ice for 15 minutes (or overnight at -20.degree. C.). (d). centrifuge at 16 000 rpm for 15 minutes and discard supernatant (e) wash pellet in 500 .mu.l cold 70% CH.sub.3 CH.sub.2 OH. Re-centrifuge (16 000 rpm 5') and discard supernatant. (f) dry pellet under vacuum for 5 minutes and resuspend in 20 .mu.l TE buffer.
Step 2--End-repair of PCR fragments
(a) to 20 .mu.l of precipitated DNA add: 3 .mu.l 10 x Ligase buffer
(Boehringer Mannheim), 1 .mu.l 12.5 mM dNTP's (Pharmacia DNA polymerisation mixture), 0.5 .mu.l (5U) E. coli DNA polymerase large (Kienow) fragment (BRL technologies Ltd), 0.25 .mu.l (2.5U) T4 DNA polymerase (Boehringer Mannheim), 0.25 .mu.l (2.5U) T4 polynucleotide kinase (Boehringer Mannheim) and H.sub.2 O up to 30 .mu.l. (b) incubate at 37.degree. C. for 30 minutes and heat-kill enzymes by incubating at 70.degree. C. for 10 minutes.
Step 3--Gel-purification of the end-repaired xylanase fragment
(a) run DNA through 2% LMP agarose in 1x Tris-acetate buffer (pH 7.8). (b) excise the 350 bp xylanase band from the agarose. (c) purify the DNA from the agarose slice using the GeneClean.RTM.) procedure (Bio101 Inc.).
Step 4--Ligation into M13mp10 (Smal-phosphatased)
(a) mix 1 .mu.l M13mp10 vector DNA (appropriately diluted to ca. 10 ng/.mu.l), 20-50 ng insert DNA (xylanase consensus primer fragment), 1 .mu.l 10x ligase buffer (Boehringer Mannheim), 1 .mu.l T4 DNA ligase (Boehringer Mannheim), and H20 up to 10 .mu.l.
(b) incubate overnight at room temperature.
Step 5--Transformation of ligation mixture into Escherichia coli strain JM101:
(a) transform JM101 with the entire 10 .mu.l ligation mixture using the DMSO-mediated transformation technique of Chung et al. (1989. Proc. Natl. Acad. Sci. 86: 2172-2175.). (b) Plate the M13/JM101, and isolate recombinant M13 plasmids using standard procedures (Sambrook et al. 1989 Cold Spring Harbour Laboratory Press).
Recombinant M13 phage containing internal xylanase consensus fragments were sequenced from ssDNA (Sambrooket at al. 1989) on an Applied Biosystems 373A automated DNA sequencer using dye-primer chemistry (sequencing primer used was the universal M13 forward {dye-labelled} primer, ABI Ltd). All, DNA sequence data were analysed and manipulated using the G C G sequence analysis software (installed on Irix) run on a Silicon Graphics Personal Iris Workstation.
Family F xylanase internal fragment sequence results
Based on the PCR fragments which were amplified from the six strains depicted in Table 1 using the xylanase consensus primers, it was predicted that each organism contained between 1 to 3 family F xylanase genes. The results have been analysed via the well known boot-strap analysis (Wisconsin Molecular Biology Package, Devereux, 1984, Nucleic. Acids Res. 12, 387-394). In FIG. 1 a dendogram of the various xylanases and strains is shown. From the nucleotide sequences of the family F consensus fragments, it now appears that each organism will contain three different family F genes. Each of the family F xylanase genes of each organism belongs to a separate xylanase cluster (based on nucleotide and primary amino acid sequence homologies), now designated as cluster A, cluster 8 and cluster C. The full-length xylanase amplified from TG 456 belongs to cluster A, and has subsequently been named TG 456 xynA. In addition, an internal consensus fragments from a TG 456 cluster B xylanase (TG 456 xynB) and a cluster C xylanase (TG 456 xync) have been identified.
EXAMPLE 7
Cloning and sequence determination of internal consensus fragments of genes encoding thermostable G-type xylanases
7.1 PCR amplification of internal fragments of G-type xylanase genes
The Family G internal consensus fragments (ICFs) were isolated with the Polymerase Chain Reaction (PCR), using the forward and reverse family G consensus primers (GF and GR). The PCR profile was as follows:
n.b. .degree.C. refers to degrees celsius.
refers to the number of cycles (i.e. x1 equals ONE cycle)
(94.degree. C., 4 minutes) x 1
(94.degree. C., 1 minute;. 45.degree. C., 1 minute; 72.degree. C., 1 minute) x 35 (94.degree. C., 1 minute;
45.degree. C., 1 minute; 72.degree. C., 6 minute) x 1
The PCRs were performed in 50 uL reactions using the following ingredients: 100 ng GF primer; 100 ng GR primer; 0.25 mM dNTPs; 1 Unit Taq Polymerase; 0.25 mM MgCl2; 10 mM Tris-HCl, pH 8.8; 50 mM KCl; 0.001% Gelatin; 1-10 ng template DNA.
Two PCR primers were used to amplify consensus fragments of xylanase genes:
GF: TATNTGRSTNTMTATGGWTGG (forward internal consensus primer) SEQ ID NO 4.
GR: CCGCTNCTTTGGTANCCTTC (reverse internal consensus primer) SEQ ID NO 5.
With all six strains a PCR fragment was found upon amplification with the consensus primers.
Two species of PCR-products (DNA fragments) were amplified: a 300 bp fragment of the expected size, plus an unexpected 600 bp PCR-product this 600 bp fragment was a head-to-tail dimer of the 300 bp PCR-product; presumably this 600 bp species was a result of self-priming during the PCR reactions, as a consequence of homology between the Gr and GR primers.
7.2 Sequence determination of the PCR products
The 300 bp fragments amplified from each organism were end-repaired (see example 6).
The end-repaired fragments were then purified from a 1% low melting temperature agarose gel (run in Tris-acetate running buffer) using the Geneclean (Bio 101, La Jolla, Calif.) procedure.
Approximately 10 ng of the end-repaired and gel-purified 300 ICFs were ligated into the Smal site of M13mp10 using BM T4 DNA ligase, in 10 uL reactions.
7.3 Sequence determination of the PCR products
Six independent phages originating from strains TG457 and TG53 were sequenced. It appears from the alignments (FIG. 2) that only a single G-type xylanase gene is present in each of these strains. In addition M13 mp 10 recombinants containing family G ICFs from TG453, TG456, TG479 and TG631 were sequenced. These organisms contained all a family G xylanase gene encoding an essentially identical xylanase, although variations in the DNA sequence are up to 13%.
EXAMPLE 8
Sequence of full-length F-type xylanases
On the basis of the internal PCR fragments 3 different type of F-xylanase genes have been identified: xynA, xynB and xynC. Using Genome Walking PCR (GWPRCR) full length xylanase genes have been isolated from most of the strains.
Full length sequences of the TG456 xynA gene have been determined. The complete sequence of the xyna gene is given in SEQ ID NO 6. The encoded amino acid sequence of the TG456 xylanase A is provided in SEQ ID NO 7.
For xynS and xynC it was discovered that the genes encode multi-domain enzymes, with one xylanase domain. These xylanase domains have been subcloned using PCR primers designed on sequences at the border of the xylanase domain.
The partial sequence information for the xynB and xynC genes originating from TG456 are given in SEQ ID NO 8 and SEQ ID NO 10, respectively. The encoded amino acid sequences of the TG456 xylanases B and C are given in SEQ ID NO 9 and SEQ ID NO 11, respectively.
EXAMPLE 9
Complete sequence of G-type xylanase genes
Using Genome Walking PCR (GWPRCR) the full length xynd genes have been isolated from most of the strains.
The complete sequence for the xynD gene of TG456 is given in SEQ ID NO 12 and the encoded TG456 xylanase D amino acid sequence is provided in SEQ ID NO 13.
EXAMPLE 10
Construction of expression vectors and hosts for xylanase production from cloned genes
In the consensus PCR primers appropriate restriction sites have been designed, which allow the subcloning of xylanase genes in suitable expression vectors.
The xynA and xynC genes are inserted Ncol-BamHl into the pJLA602 expression vector [Schauder, B., Blucker, H., Frank, R., and McCarthy, J. E. G. (1987). Inducible Expression Vectors Incorporating the Escherichia coli atpE Transcriptional Initiation Region. Gene 52: 279-283.]) for in-frame fusion with the lambda L and R promoters [Gibbs, M. G, Saul D. J, Luthi, E., and Bergquist, P. L. (1992). The beta-mannanase from "Caldocellum saccharolyticum" is Part of a Multidomain Enzyme. AppI. Environ. Microbiol. 58 (12): 3864-3867.]
XynB and xynD genes were inserted into the unique SphI-BamHI sites of pJLA602.
Constructs were transferred into the hosts E.coli JM101 and E.coli DHS.alpha. using standard transformation techniques.
FIG. 3 shows the sequence of the xylanase domain of xynD from TG456 inserted in pJLA602 as a SphI-BamHI fragment.
EXAMPLE 11
Production and recovery of cloned xylanases
In order to obtain protein samples from the cloned F-type xylanases the E.coli clones were fermented in a 10.0 liter capacity LH fermenter (series 210). The culture was maintained at 30.degree. C. until induction (42.degree. C.) with continuous aeration (4.8 liters/min), agitation (500 rpm) and pH control (pH 7.1). The media used and other additions are given below:
______________________________________ Luria Broth (for inoculum cultures): Tryptone 10 g Yeast Extract 5 g NaCl 10 g Water to 1000 ml BGM2 bulk growth medium for fermenter runs (quantities are for final medium, i.e. 2 batches of 8.5 liters): NH.sub.4 Cl 3.22 g KH.sub.2 PO.sub.4 1.05 g MgSO.sub.4.7H.sub.2 C 0.135 g K.sub.2 SO.sub.4 0.043 g FeSO.sub.4.7H.sub.2 0 0.003 g SL-10 Trace Elements 1 ml Tryptone 10 g Yeast Extract 4.7 g Glycerol 34 ml Water to 1000 ml______________________________________
After the fermenter vessel, with approximately 6 liters of water in it, was sterilized by autoclaving at 121.degree. C. for 30 minutes, it was cooled to 30.degree. C. The media concentrate (8.5 fold concentrate) was pumped through a sterile 0.2 .mu.m cartridge filter (Sartorius). Prior to inoculation the following additions were made:
______________________________________ Antifoam (Bevaloid 5901) 10 ml (autoclaved) CaCl.sub.2 (17 mg/ml stock) 1 ml (autoclaved) Ampicillin 850 mg (filter sterilized) Thiamine (JM101 cultures only) 8.7 mg (filter sterilized)______________________________________
The liquid volume was then adjusted to. 8.5 liters. The pH of the media was adjusted to 7.1. Filter-sterilized air was sparged through the fermenter at a flow rate of 4.8 liters per minute. The fermenter temperature was held at 30.degree. C. by hot and cold water circulation through finger probes. pH control was by addition of autoclaved NaOH (5M) or H.sub.4 SO.sub.4 (2M). The fermenter stirrer speed was 500 rpm.
Inoculation was initiated with an aliquot (approximately 10.0 ml) of a fresh culture of the E.coli clone grown in Luria Broth with 100 .mu.g/mi ampicillin at an OD.sub.650 of 0.2 to 0.4. The cells were grown to an OD.sub.650 of between 11 and 13 at 30.degree. C., then they fed-batched with a medium concentrate, allowed to recover and grown to an OD.sub.650 of between 14 and 16. They were subsequently induced by raising the temperature to 42.degree. C.
The cells were harvested 4 hours after maximum OD.sub.650 was reached. The cells were recovered by hollow fibre filtration (0.1 .mu.m, Amicon) and resuspended in 50 mM Tris-HCl (pH 8.0), 7.5 mM EDTA, 7.5 mM .beta.-mercaptoethanol, 0.02% PMSF, 1.0 .mu.M pepstatin A, 0.02% DNase and 0.02% lysozyme and incubated at 4.degree. C. for 1 hour (total volume of approximately 1 liter). The cells were sonicated on ice in 160 ml batches for 4-6 minutes in one minute blasts until lysed (monitored by microscopys). An aliquot of 56 mM PMSF (in isopropanol) was added (each addition equivalent to 160 .mu.M) for each two minutes of sonication to a final concentration of no more than 1 mM PMSF. After lysis was complete, cell debris was removed by centrifugation. The supernatant was heat treated at 70.degree. C. until obvious precipitation of protein occurred (usually about 20-30 minutes) and the denatured protein was removed by centrifugation. Prior to phenyl-sepharose chromatography, ammonium sulphate was added to the heat-treated supernatant to a final concentration of 1.0M (this is termed the 1.degree. heat treatment extract). The cell pellet derived from the sonicated cells was re-extracted by suspension in 1.0 liter of 50 mM Tris-HCl (pH 8.0), 5 mM EDTA, 7 mM .beta.-mercaptoethanol, followed by a second heat treatment at 70.degree. C. for 15 minutes and the precipitated protein was again removed by centrifugation. This was found to extract an additional 20-40% of the xylanase and was termed 2.degree. heat treatment extract. Ammonium sulphate was added to this 2.degree. heat treatment extract to 1.0M and the 10 and 2.degree. heat treatment extracts were pooled prior to phenyl-sepharose separation. Xylanase activity was step-eluted from the 1100 ml bed volume phenyl-sepharose column (after extensive washing with 1.0M ammonium sulphate and return to baseline) using 1.0M NaCl and the eluted protein was concentrated and desalted by ultrafiltration with a YM3 membrane (Amico). The final concentration of the preparations are 25 mM Tris-HCl (pH 8.0), 5 mM EDTA, 7 mM .beta.-mercaptoethanol, approximately 250 mM NaCl, 20% glycerol and 0.05% sodium azide.
For production of the G-type xylanases the method was nearly identical to that described above except that HEPES buffer was used in place of TrisHCl for both the extraction (pH 8.0) and the desalting (pH 7.3) steps. The final preparation had a buffer composition of 50 mM HEPES, pH 7.3, 1 mM EDTA, 7 mM .beta.-meraptoethanol, 0.05% sodium Azide, 20.0% glycerol and .+-.250 mM NaCl.
In total 6 F-type preparations (5 xynA and 1 xynB) and 2 G-type preparation of sufficient purity were obtained. For both the F-type and, the G-type preparation the protein concentration was determined by the standard BCA method (Pierce, Rockford, Ill., USA). The purity of the samples was roughly estimated by running an SDS-PAGE gel (Phast-system, Pharmacia, 20% gel) and comparing the thickness of the band at about 40 kDa for the F-type, and about 25 kDa for the G-type with the thickness of the bands of the impurities. The purity of the samples varied between 20 and 70% (Table 9).
TABLE 9______________________________________Purity of F-type and G-type xylanase preparations Enzyme Purity (%)______________________________________TG53 xynA 30 TG53 xynD (G-type) 20 TG456 xynA 70 TG456 xynD (G-type) 30 TG457 xynA 70 TG479 xynA 70 TG631 xynA 70 TG631 xynB 20______________________________________
EXAMPLE 12
ECF bleaching results with cloned F- and G-type xylanases
ECF-bleaching was performed using oxygen delignified Kraft pulp from a Swedish pulp mill. The softwood (SW) pulp had a kappa number of 16.0 and the hardwood (HW) pulp a kappa number of 10.6. A XDED-sequence was used under conditions as presented in Table 10.
TABLE 10______________________________________Bleaching conditions STAGE X D.sub.0 E D.sub.1______________________________________Cons 10% 10% 10% 10% Time 120 min 60 min 60 min 120 min. Temp 65.degree. C. 60.degree. C. 60.degree. C. 70.degree. C. pH 9 .congruent. 2.5 .congruent. 10 .congruent. 3.5 Chemical 15 .mu.g xyl. chlorine mul- NaOH: aCl.sub.2 : Dosage protein/ tiple: 0.15 7.2 kg/t 10 kg/t g pulp (SW) (S/HW) 5.9 kg/t (HW)______________________________________ X = enzyme, D.sub.0, D.sub.1 = chlorine dioxide, E = extraction with NaOH.
The results of these experiments are presented in Table 11. It can be seen that the G-type xylanases perform significantly better as compared with the F-type xylanases, when compared on the basis of enzyme protein.
TABLE 11______________________________________ECF bleaching with cloned F- and G-type xylanases. Delta brightness (% ISO) Enzyme SW HW______________________________________TG53xynA 1.0.sup.2) 1.2.sup.5 TG53xynD (G-type) 5.9.sup.3) /6.8.sup.4) 3.0.sup.6) TG456xynA 1.2.sup.1) /0.7.sup.2) 1.0.sup.5) TG456xynD (G-type) 4.3.sup.3) /5.9.sup.4) 4.0.sup.5) /2.1.sup.6) TG457xynA 0.sup.1) 0.sup.6) TG479xynA 0.3.sup.2)0.3.sup.5) TG631xynA 0.sup.1) 0.sup.6) TG631xynB 0.sup.2) --______________________________________ .sup.1)-6) refer to six separate experiments. The reference ISO brightness values of these experiments were as follows: expt 1: 73.5; exp 2: 78.3; expt 3: 52.0; expt 4: 52.3; expt 5: 79:0; expt 6: 80.5.
EXAMPLE 13
ECF dose-response curves with cloned G-type xylanases
Using the same XDED bleaching sequence as described in Example 12 the dosage of the two G-type xylanases was varied. The results are shown in Table 12. Dosages of 1 to 3 .mu.g/g pulp already give an increase in ISO brightness of at least two points.
TABLE 12__________________________________________________________________________Dose-response curves of two G-type xylanases dosage Brightness HW Brightness SW (.mu.g xyl/ (XDED) (XDED)Enzyme g pulp) % ISO .DELTA. % ISO % ISO .DELTA. % ISO % ISO .DELTA. % ISO__________________________________________________________________________TG456 xynD 0 78.5 -- 55.85 -- 62.92 -- 1 80.73 2.23 56.80 0.95 65.73 2.81 3 81.03 2.53 58.06 2.21 68.12 5.20 6 80.99 2.49 59.20 3.35 68.32 5.40 15 70.45 7.53 TG3 xynD 0 78.5 -- 55.85 -- 66.75 -- 1 79.73 1.23 57.28 1.43 69.04 2.29 3 80.13 1.63 57.87 2.02 69.35 2.60 6 81.32 2.82 58.23 2.38 69.92 3.17 15 72.39 5.64__________________________________________________________________________
EXAMPLE 14
TCF bleaching results with cloned G-type xylanases
The two G-type xylanases were tested in a TCF bleaching sequence using the XQPP sequence as described in Example 15 (below). Oxygen delignified hardwood kraftpulp was used (30 g o.d. per sample). The dosage of the G-type xylanases was varied as indicated in Table 13. ISO brightness values obtained for each sample after X, P1 and P2 stages are given in Table 13. The value represent the average of duplicate samples.
TABLE 13______________________________________TCF bleaching - dose response experiment with G-type xylanases. dosage (.mu.g protein/ X P1 P2 Sample g. pulp) brightness brightness brightness______________________________________Control 0 50.3 79.5 81.0 TG456 xynD 15 53.8 81.8 84.3 6 52.9 81.0 83.8 TG53 xynD 15 55.2 82.2 85.1 6 53.6 82.7______________________________________ 85.1
The experiment was repeated using dosages of 3 and 6 .mu.g protein per g pulp. Only the brightness values obtained after the P2 stage were determined. Results are presented in Table 14.
TABLE 14______________________________________TCF bleaching - dose response experiment with G-type xylanases dosage (.mu.g Sample protein/g pulp) P2 brightness______________________________________Control 0 84.5 TG466 xynD 6 85.5 3 86.5 TG53 xynD 6 86.1 3 86.8______________________________________
EXAMPLE 15
ECF and TCF results, including paper properties
Xylanase samples were tested for bleaching effect in ECF & TCF bleaching of a Kraft H/W and a Kraft S/W pulp supplied from a Swedish pulp mill. The cloned TG456 xynD and TG53 xynD (in this Example referred to as 715 and 716, respectively) are compared with "no-enzyme" reference samples. The refining tests in a Lampen ball mill showed that 715 gave the overall best performance with considerable improvements in Tear Index and no significant loss in Tensile and Burst Indices.
Screening Protocol
______________________________________ Hardwood Softwood______________________________________1. TCF Ref QPP 1. TCF Ref QPP 2. Enz 715 XQPP 2. Enz 715 XQPP 3. Enz 716 XQPP 3. Enz 716 XQPP 4. ECF Ref No X DEDED 4. ECF Ref No X DEDED 5. Enz 715 XDEDED 5. Enz 715 XDEDED 6. Enz 716 XDEDED 6. Enz 716 XDEDED 7. Chem Ref DEDED 7. Chem Ref DEDED______________________________________Unbleached pulp properties % ISO Bright- Viscosity Pulp Kappa No ness dm.sup. /kg______________________________________ Kraft H/W 10.8 53 1104 Kraft S/W 16.1 36.4 1003______________________________________Bleaching parameters to be tested % ISO Chemical Paper Brightness consumption Kappa No Viscosity Strength______________________________________ TCF After X XQP XQPP XQPP XQPP XQP XQPP XQPP ECF AfterX XDE XDE XDEDED XDEDED XDE XDED XDED XDEDED XDEDED______________________________________Bleaching conditions A) TCF H/W & S/W (Same bleaching conditions for both pulps) Stage X Q P P______________________________________ Consistency (%) 10 9 10 10 Time (mins) 120 5*4 secs in 180 180 mixer Temp. (.degree. C.) 65 65 85 85 pH 9 4-5 10.5-11 10.5-11 Enz Charge 3 -- -- -- EDTA Charge -- 3 -- -- (kg/t) NaOH Charge -- -- 20 10 (kg/t) H.sub.2 O.sub.2 Charge -- -- 20 10 (kg/t)______________________________________B) ECF H/W X Stage D E D E D______________________________________ Consistency 10 10 10 10 10 10 (%) Time (mins) 120 60 60 120 60 180 Temp (.degree. C.) 65 60 60 70 60 70 pH 9 2-3 .about.11.5 2.5-3 .about.11.5 4-5 Enz Charge 3 -- -- -- -- -- (.mu.g/g) aCl Charge -- 0.18* -- 18 -- 8 (kg/t) Kappa = 19.4 for X ref & all X's 21.6 for Chem Ref NaOH -- -- 11.6 for X -- 10 -- Charge ref & all (kg/t) X's 13 for Chem Ref______________________________________C) ECF S/W X Stage D E D E D______________________________________ Consistency 10 10 10 10 10 10 (%) Time (mins) 120 60 60 120 60 180 Temp (.degree. C.) 65 60 60 70 60 70 pH 9 2-3 .about.11.5 2.5-3 .about.11.5 4-5 Enz Charge 3 -- -- -- -- -- (.mu.g/g) aCl Charge -- 0.18* -- 18 -- 8 (kg/t) Kappa = 28.8 for X ref & all X's 32 for Chem Ref NaOH -- -- 17.3 for X -- 10 -- Charge ref & all (kg/t) X's 19.2 for Chem Ref______________________________________
The results obtained in the above experiments are present in Tables 15 (Hardwood) and 16 (Softwood).
TABLE 15______________________________________A summary of the Hardwood bleaching results Hardwood______________________________________ P2 % P2 ISO Kappa P2 Visc Total P______________________________________ TCF Ref 78.4 6.7 866 25.2 TCF 715 81 6.2 850 26.1 ++- TCF 716 81.7 6.2 740 27.7 ++-______________________________________ D2 % XDE ISO Kappa D2 Visc Total aCl______________________________________ ECF Ref 88.6 4.6 1050 46.1 ECF 715 89.1 4.5 1035 44.8 ++-+ ECF 716 88.6 4.6 1040 45 00-+ Chem Ref 88.6 4.9 1020 47______________________________________
TABLE 16______________________________________A summary of the Softwood bleaching results. Softwood______________________________________ P2 % P2 ISO Kappa P2 Visc Total P______________________________________ TCF Ref 69.1 7.3 814 18.5 TCF 715 72.1 6.7 805 16 ++-+ TCF 716 71 6.7 833 16.7 +++ D2 % XDE ISO Kappa D2 Visc Total aCl______________________________________ ECF Ref 85.5 4.6 941 54.5 ECF 715 86.5 4.4 935 54.4 ++-0 ECF 716 86.7 4.3 935 54.5 ++-0 Chem Ref 87.5 3.7 962 57.3______________________________________
Verification of paper Properties
After all the sequences were fully bleached, 30 g samples were taken and refined in a Lampen ball mill for 10, 20 and 30 thousand revolutions. Schopper-Rieglers were measured, after which approximately 2 g sheets were made for Tensile Index, Porosity, Tear Index and Burst Index. The sheets were left to condition for 24 hours at 23.degree. C. and 50% relative humidity. The results obtained are presented in FIGS. 4 to 8.
EXAMPLE 16
pH optimum, temperature optimum and thermostability of TG456 xynD
Activities were measured as described in Example 2, procedure 1, with oat spelt xylane as substrate. All assays were performed in 50 mM phosphate buffer, at the pH and temperature as indicated. The results are presented in FIGS. 9 and 10.
The TG456 xylanase D is much more thermostable than the reference enzyme Pulpzyme HB (Novo Nordisk), and it has a slightly higher pH optimum
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 13 - - - - (2) INFORMATION FOR SEQ ID NO: 1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 17 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (C) INDIVIDUAL ISOLATE: - #xynFA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #1: - - CACACKCTKG TKTGGCA - # - # - # 17 - - - - (2) INFORMATION FOR SEQ ID NO: 2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 17 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (C) INDIVIDUAL ISOLATE: - #xynFB - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #2: - - CATACKTTKG TTTGGCA - # - # - # 17 - - - - (2) INFORMATION FOR SEQ ID NO: 3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 17 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: YES - - (vi) ORIGINAL SOURCE: (C) INDIVIDUAL ISOLATE: - #xynR - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #3: - - TMGTTKACMA CRTCCCA - # - # - # 17 - - - - (2) INFORMATION FOR SEQ ID NO: 4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 21 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (C) INDIVIDUAL ISOLATE: - #GF - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #4: - - TATNTGRSTN TMTATGGWTG G - # - # - #21 - - - - (2) INFORMATION FOR SEQ ID NO: 5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: YES - - (vi) ORIGINAL SOURCE: (C) INDIVIDUAL ISOLATE: - #GR - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #5: - - CCGCTNCTTT GGTANCCTTC - # - # - # 20 - - - - (2) INFORMATION FOR SEQ ID NO: 6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1065 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (A) ORGANISM: Extremophile (C) INDIVIDUAL ISOLATE: - #TG456 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 3..1058 (D) OTHER INFORMATION: - #/product= "xylanase A" /gene= - #"xynA" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #6: - - CC ATG GAC CTT TAT TCA ATC TCA GAT GAA AAT - # TGG GGG CAG CCT GTG 47 Met Asp Leu Tyr Ser Ile Ser Asp Glu - #Asn Trp Gly Gln Pro Val 1 - # 5 - # 10 - # 15 - - CCT GAT TAT AAA CTG CCA TCA CTT TGT GAA AA - #G TAC AAA AAC TAT TTC 95 Pro Asp Tyr Lys Leu Pro Ser Leu Cys Glu Ly - #s Tyr Lys Asn Tyr Phe 20 - # 25 - # 30 - - AAG ATT GGA GTT GCT GTG CCC TAC AGG GCT CT - #G ACA AAT CCA GTT GAT 143 Lys Ile Gly Val Ala Val Pro Tyr Arg Ala Le - #u Thr Asn Pro Val Asp 35 - # 40 - # 45 - - GTG GAG ATG ATA AAA AGG CAT TTC AAC AGC AT - #A ACA CCG GAG AAC GAG 191 Val Glu Met Ile Lys Arg His Phe Asn Ser Il - #e Thr Pro Glu Asn Glu 50 - # 55 - # 60 - - ATG AAA CCA GAG AGC CTT CAG CCT TAT GAA GG - #T GGT TTT AGC TTT AGC 239 Met Lys Pro Glu Ser Leu Gln Pro Tyr Glu Gl - #y Gly Phe Ser Phe Ser 65 - # 70 - # 75 - - ATT GCA GAT GAG TAT ATA GAT TTT TGC AAA AA - #G AAC AAT ATC TCA CTG 287 Ile Ala Asp Glu Tyr Ile Asp Phe Cys Lys Ly - #s Asn Asn Ile Ser Leu 80 - # 85 - # 90 - # 95 - - CGA GGG CAC ACK CTT GTT TGG CAT CAG CAA AC - #C CCG AGC TGG TTC TTT 335 Arg Gly His Thr Leu Val Trp His Gln Gln Th - #r Pro Ser Trp Phe Phe 100 - # 105 - # 110 - - ACA AAT CCT GAG ACG GGC GAA AAA CTT ACT AA - #C AGT GAG AAG GAC AAG 383 Thr Asn Pro Glu Thr Gly Glu Lys Leu Thr As - #n Ser Glu Lys Asp Lys 115 - # 120 - # 125 - - RAA ATA CTA TTG GAT AGG CTA AAG AAG CAC AT - #C CAG ACA GTT GTT GGC 431 Xaa Ile Leu Leu Asp Arg Leu Lys Lys His Il - #e Gln Thr Val Val Gly 130 - # 135 - # 140 - - AGG TAT AAG GGG AAA GTA TAT GCA TGG GAC GT - #T GTG AAT GAG GCG ATT 479 Arg Tyr Lys Gly Lys Val Tyr Ala Trp Asp Va - #l Val Asn Glu Ala Ile 145 - # 150 - # 155 - - GAT GAG AAT CAG CCG GAT GGG TAT AGA AGA AG - #T GAC TGG TAC AAT ATC 527 Asp Glu Asn Gln Pro Asp Gly Tyr Arg Arg Se - #r Asp Trp Tyr Asn Ile 160 1 - #65 1 - #70 1 -#75 - - TTR GGA CCG GAG TAC ATT GAA AAG GCA TTT AT - #C TGG GCG CAT GAAGCA 575 Xaa Gly Pro Glu Tyr Ile Glu Lys Ala Phe Il - #e Trp Ala His Glu Ala 180 - # 185 - # 190 - - GAC CCG AAA GCA AAG CTT TTC TAC AAT GAC TA - #C AGT ACA GAA GAM CCA 623 Asp Pro Lys Ala Lys Leu Phe Tyr Asn Asp Ty - #r Ser Thr Glu Xaa Pro 195 - # 200 - # 205 - - TAT AAA AGA GGG AAT TTA TAT ACA CTA ATT AA - #A AAY TTA AAA GCM AAA 671 Tyr Lys Arg Gly Asn Leu Tyr Thr Leu Ile Ly - #s Asn Leu Lys Ala Lys 210 - # 215 - # 220 - - GGT GTG CCA GTT CAT GGT GTT GGG CTT CAG TG - #T CAT ATT TCA CTT GAC 719 Gly Val Pro Val His Gly Val Gly Leu Gln Cy - #s His Ile Ser Leu Asp 225 - # 230 - # 235 - - TGG CCG GAT GTG AGT GAA ATC GAG GAG ACT GT - #C AAA TTA TTT AGC AGG 767 Trp Pro Asp Val Ser Glu Ile Glu Glu Thr Va - #l Lys Leu Phe Ser Arg 240 2 - #45 2 - #50 2 -#55 - - ATT CCA GGA CTT GAA ATA CAC TTC ACA GAA AT - #T GAT ATA AGT ATTGCT 815 Ile Pro Gly Leu Glu Ile His Phe Thr Glu Il - #e Asp Ile Ser Ile Ala 260 - # 265 - # 270 - - AAA AAC ATG ACC GAT GAT GAT GCA TAT AAC CG - #C TAT CTT TTG ATT CAG 863 Lys Asn Met Thr Asp Asp Asp Ala Tyr Asn Ar - #g Tyr Leu Leu Ile Gln 275 - # 280 - # 285 - - CAG GCA CAA AAA TTA AAA GCA ATT TTT GAT GT - #T TTG AAA AAG TAC AGA 911 Gln Ala Gln Lys Leu Lys Ala Ile Phe Asp Va - #l Leu Lys Lys Tyr Arg 290 - # 295 - # 300 - - AAT GTA GTT ACA AGT GTT ACA TTC TGG GGA CT - #G AAG GAT GAT TAC TCA 959 Asn Val Val Thr Ser Val Thr Phe Trp Gly Le - #u Lys Asp Asp Tyr Ser 305 - # 310 - # 315 - - TGG CTA CGG GGA GAT ATG CCA CTT TTA TTC GA - #T AAA GAC TAC CAG CCA 1007 Trp Leu Arg Gly Asp Met Pro Leu Leu Phe As - #p Lys Asp Tyr Gln Pro 320 3 - #25 3 - #30 3 -#35 - - AAG TTT GCG TTC TGG AGC TTA ATT GAC CCA TC - #A GTT GTC CCA AAAGAG 1055 Lys Phe Ala Phe Trp Ser Leu Ile Asp Pro Se - #r Val Val Pro Lys Glu 340 - # 345 - # 350 - - TAATGGATCC - # - #- # 1065 - - - - (2) INFORMATION FOR SEQ ID NO: 7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 351 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #7: - - Met Asp Leu Tyr Ser Ile Ser Asp Glu Asn Tr - #p Gly Gln Pro Val Pro 1 5 - # 10 - # 15 - - Asp Tyr Lys Leu Pro Ser Leu Cys Glu Lys Ty - #r Lys Asn Tyr Phe Lys 20 - # 25 - # 30 - - Ile Gly Val Ala Val Pro Tyr Arg Ala Leu Th - #r Asn Pro Val Asp Val 35 - # 40 - # 45 - - Glu Met Ile Lys Arg His Phe Asn Ser Ile Th - #r Pro Glu Asn Glu Met 50 - # 55 - # 60 - - Lys Pro Glu Ser Leu Gln Pro Tyr Glu Gly Gl - #y Phe Ser Phe Ser Ile 65 - # 70 - # 75 - # 80 - - Ala Asp Glu Tyr Ile Asp Phe Cys Lys Lys As - #n Asn Ile Ser Leu Arg 85 - # 90 - # 95 - - Gly His Thr Leu Val Trp His Gln Gln Thr Pr - #o Ser Trp Phe Phe Thr 100 - # 105 - # 110 - - Asn Pro Glu Thr Gly Glu Lys Leu Thr Asn Se - #r Glu Lys Asp Lys Xaa 115 - # 120 - # 125 - - Ile Leu Leu Asp Arg Leu Lys Lys His Ile Gl - #n Thr Val Val Gly Arg 130 - # 135 - # 140 - - Tyr Lys Gly Lys Val Tyr Ala Trp Asp Val Va - #l Asn Glu Ala Ile Asp 145 1 - #50 1 - #55 1 -#60 - - Glu Asn Gln Pro Asp Gly Tyr Arg Arg Ser As - #p Trp Tyr Asn IleXaa 165 - # 170 - # 175 - - Gly Pro Glu Tyr Ile Glu Lys Ala Phe Ile Tr - #p Ala His Glu Ala Asp 180 - # 185 - # 190 - - Pro Lys Ala Lys Leu Phe Tyr Asn Asp Tyr Se - #r Thr Glu Xaa Pro Tyr 195 - # 200 - # 205 - - Lys Arg Gly Asn Leu Tyr Thr Leu Ile Lys As - #n Leu Lys Ala Lys Gly 210 - # 215 - # 220 - - Val Pro Val His Gly Val Gly Leu Gln Cys Hi - #s Ile Ser Leu Asp Trp 225 2 - #30 2 - #35 2 -#40 - - Pro Asp Val Ser Glu Ile Glu Glu Thr Val Ly - #s Leu Phe Ser ArgIle 245 - # 250 - # 255 - - Pro Gly Leu Glu Ile His Phe Thr Glu Ile As - #p Ile Ser Ile Ala Lys 260 - # 265 - # 270 - - Asn Met Thr Asp Asp Asp Ala Tyr Asn Arg Ty - #r Leu Leu Ile Gln Gln 275 - # 280 - # 285 - - Ala Gln Lys Leu Lys Ala Ile Phe Asp Val Le - #u Lys Lys Tyr Arg Asn 290 - # 295 - # 300 - - Val Val Thr Ser Val Thr Phe Trp Gly Leu Ly - #s Asp Asp Tyr Ser Trp 305 3 - #10 3 - #15 3 -#20 - - Leu Arg Gly Asp Met Pro Leu Leu Phe Asp Ly - #s Asp Tyr Gln ProLys 325 - # 330 - # 335 - - Phe Ala Phe Trp Ser Leu Ile Asp Pro Ser Va - #l Val Pro Lys Glu 340 - # 345 - # 350 - - - - (2) INFORMATION FOR SEQ ID NO: 8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1633 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (A) ORGANISM: Extremophile (C) INDIVIDUAL ISOLATE: - #TG456 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..1632 (D) OTHER INFORMATION: - #/partial /product=- # "xylanase B" /gene= - #"xynB" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #8: - - TGT ACC ATA AAA TGG CAG CAA ACA GTT CCA TC - #T GGG GTT TGG ACA GAA 48 Cys Thr Ile Lys Trp Gln Gln Thr Val Pro Se - #r Gly Val Trp Thr Glu 1 5 - # 10 - # 15 - - GTT TCT GGT TCA TAT ACA GTA CCA CAG ACA GC - #A ACC CAG CTC ATA TTC 96 Val Ser Gly Ser Tyr Thr Val Pro Gln Thr Al - #a Thr Gln Leu Ile Phe 20 - # 25 - # 30 - - TAT GTG GAA TCG CCA AAT GCA ACA CTT GAC TT - #T TAC CTT GAC GAC TTT 144 Tyr Val Glu Ser Pro Asn Ala Thr Leu Asp Ph - #e Tyr Leu Asp Asp Phe 35 - # 40 - # 45 - - ACT GTA ATA GAC AAA AAC CCG GTT ACA ATA CC - #T GCT GCG GCA AAA GAG 192 Thr Val Ile Asp Lys Asn Pro Val Thr Ile Pr - #o Ala Ala Ala Lys Glu 50 - # 55 - # 60 - - CCA GAG TTG GAG ATT CCA TCA CTT TGC CAG CA - #A TAC AGC CAG TAC TTT 240 Pro Glu Leu Glu Ile Pro Ser Leu Cys Gln Gl - #n Tyr Ser Gln Tyr Phe 65 - # 70 - # 75 - # 80 - - TCA ATT GGT GTT GCA ATA CCA TAT AGA GTG CT - #C CAA AAC CCG GTA GAA 288 Ser Ile Gly Val Ala Ile Pro Tyr Arg Val Le - #u Gln Asn Pro Val Glu 85 - # 90 - # 95 - - AGA GCA ATG GTT TTA AAG CAT TTC AAC AGT AT - #T ACT GCT GAA AAT GAG 336 Arg Ala Met Val Leu Lys His Phe Asn Ser Il - #e Thr Ala Glu Asn Glu 100 - # 105 - # 110 - - ATG AAG CCC GAT GCT ATA CAA AGA ACA GAA GG - #G CAG TTC AAT TTC GAT 384 Met Lys Pro Asp Ala Ile Gln Arg Thr Glu Gl - #y Gln Phe Asn Phe Asp 115 - # 120 - # 125 - - GTT GCA GAC CAG TAT GTT GAC TTT GCA CAG AG - #C AAT AAT ATT GGA ATA 432 Val Ala Asp Gln Tyr Val Asp Phe Ala Gln Se - #r Asn Asn Ile Gly Ile 130 - # 135 - # 140 - - AGA GGT CAT ACA CTG GTT TGG CAT CAA CAA AC - #T CCA GAT TGG TTT TTC 480 Arg Gly His Thr Leu Val Trp His Gln Gln Th - #r Pro Asp Trp Phe Phe 145 1 - #50 1 - #55 1 -#60 - - CAG CAT TCT GAC GGT TCG CCA CTT GAT CCA AA - #C AAT TCT GAA GACAAG 528 Gln His Ser Asp Gly Ser Pro Leu Asp Pro As - #n Asn Ser Glu Asp Lys 165 - # 170 - # 175 - - CAG CTT TTG AGA AAT AGG TTA AAA ACA CAC AT - #T CAG ACA CTT GTT GGA 576 Gln Leu Leu Arg Asn Arg Leu Lys Thr His Il - #e Gln Thr Leu Val Gly 180 - # 185 - # 190 - - AGA TAT GCA GAG AAA GTT TAT GCA TGG GAT GT - #T GTA AAT GAA GCA ATT 624 Arg Tyr Ala Glu Lys Val Tyr Ala Trp Asp Va - #l Val Asn Glu Ala Ile 195 - # 200 - # 205 - - GAT GAA AAT CAA CCG GAT GGA TAT AGA AGA AG - #T GAA TGG TAC AGA ATT 672 Asp Glu Asn Gln Pro Asp Gly Tyr Arg Arg Se - #r Glu Trp Tyr Arg Ile 210 - # 215 - # 220 - - TTA GGA CCA ACT CCA GAA ACA GGC GGA ATA CC - #A GAG TAT ATA ATC CTT 720 Leu Gly Pro Thr Pro Glu Thr Gly Gly Ile Pr - #o Glu Tyr Ile Ile Leu 225 2 - #30 2 - #35 2 -#40 - - GCA TTC CAG TAT GCA CGG GAA GCT GAC CCG AA - #C GCA AAA CTT TTCTAC 768 Ala Phe Gln Tyr Ala Arg Glu Ala Asp Pro As - #n Ala Lys Leu Phe Tyr 245 - # 250 - # 255 - - AAC GAT TAC AGC ACT GAA AAT CCA AAG AAG AG - #A CAG TTT ATT TAC AAC 816 Asn Asp Tyr Ser Thr Glu Asn Pro Lys Lys Ar - #g Gln Phe Ile Tyr Asn 260 - # 265 - # 270 - - ATG GTC AAA GCT TTG CAT GAT AGA GGT CTC AT - #T GAT GGT GTT GGT CTG 864 Met Val Lys Ala Leu His Asp Arg Gly Leu Il - #e Asp Gly Val Gly Leu 275 - # 280 - # 285 - - CAG GGA CAT ATT AAT GTG GAT TCG CCT GCA GT - #C AAA GAA ATA GAA GAT 912 Gln Gly His Ile Asn Val Asp Ser Pro Ala Va - #l Lys Glu Ile Glu Asp 290 - # 295 - # 300 - - ACA ATC AAT TTA TTC AGC ACA ATA CCG GGT CT - #T CAA ATT CAA ATA ACA 960 Thr Ile Asn Leu Phe Ser Thr Ile Pro Gly Le - #u Gln Ile Gln Ile Thr 305 3 - #10 3 - #15 3 -#20 - - GAG CTT GAT ATC AGC GTA TAT ACA AGC AGC AC - #T CAG CAA TAT GACACA 1008 Glu Leu Asp Ile Ser Val Tyr Thr Ser Ser Th - #r Gln Gln Tyr Asp Thr 325 - # 330 - # 335 - - TTA CCA CAG GAT ATT ATG ATT AAA CAG GCT TT - #A AAA TTC AAA GAG CTG 1056 Leu Pro Gln Asp Ile Met Ile Lys Gln Ala Le - #u Lys Phe Lys Glu Leu 340 - # 345 - # 350 - - TTT GAA ATG TTA AAG CGC CAC AGC GAC AGA AT - #C ACA AAT GTT ACA CTT 1104 Phe Glu Met Leu Lys Arg His Ser Asp Arg Il - #e Thr Asn Val Thr Leu 355 - # 360 - # 365 - - TGG GGT CTC AAA GAT GAT TAT CCA TGG CTG TC - #A AAA GAT AGA AGT AAC 1152 Trp Gly Leu Lys Asp Asp Tyr Pro Trp Leu Se - #r Lys Asp Arg Ser Asn 370 - # 375 - # 380 - - TGG CCA CTG CTA TTT GAT AGT AAC TAC CAG GC - #A AAA TAC AAT TAC TGG 1200 Trp Pro Leu Leu Phe Asp Ser Asn Tyr Gln Al - #a Lys Tyr Asn Tyr Trp 385 3 - #90 3 - #95 4 -#00 - - GCT ATT GTA GAA CCT TCG GTG TTG CCT GTT GC - #T ATA AAT AAG GGATAT 1248 Ala Ile Val Glu Pro Ser Val Leu Pro Val Al - #a Ile Asn Lys Gly Tyr 405 - # 410 - # 415 - - GCG AAC AAT GCA CAG CCA AGA ATT GAT GGG AT - #T ATG GAT AAA GAA TAC 1296 Ala Asn Asn Ala Gln Pro Arg Ile Asp Gly Il - #e Met Asp Lys Glu Tyr 420 - # 425 - # 430 - - AAA GGA ACC ATT CCA CTT TCG GTT TTG AAT GA - #T GCA GGG CAG GAT ATT 1344 Lys Gly Thr Ile Pro Leu Ser Val Leu Asn As - #p Ala Gly Gln Asp Ile 435 - # 440 - # 445 - - GCT CAG GTA AGG GCA CTG TGG AGT GGC AAT GA - #G CTT TGT CTT TAT GTC 1392 Ala Gln Val Arg Ala Leu Trp Ser Gly Asn Gl - #u Leu Cys Leu Tyr Val 450 - # 455 - # 460 - - ACT GTA AAT GAT TCA AGT GTG GAT GCT AAC AA - #T GAT AGG GTT GTA ATT 1440 Thr Val Asn Asp Ser Ser Val Asp Ala Asn As - #n Asp Arg Val Val Ile 465 4 - #70 4 - #75 4 -#80 - - TTC ATT GAT CAG GAC AAT GGA AAG TTG CCA GA - #G TTA AAA GAT GATGAC 1488 Phe Ile Asp Gln Asp Asn Gly Lys Leu Pro Gl - #u Leu Lys Asp Asp Asp 485 - # 490 - # 495 - - TTC TGG GTT TCA ATT TCG AGA AAT GGC ACA AA - #G AAT CAA TCC AAA ACT 1536 Phe Trp Val Ser Ile Ser Arg Asn Gly Thr Ly - #s Asn Gln Ser Lys Thr 500 - # 505 - # 510 - - GGC TAT GTA AAA GAT TAT GTA GTG TTA CAG CA - #A TTA AAT GGA TAT ACA 1584 Gly Tyr Val Lys Asp Tyr Val Val Leu Gln Gl - #n Leu Asn Gly Tyr Thr 515 - # 520 - # 525 - - ATG GAG GTT AAG CTG CTT TTA AAC AAC AGT TT - #A GCA ATT AAC ACA AAT 1632 Met Glu Val Lys Leu Leu Leu Asn Asn Ser Le - #u Ala Ile Asn Thr Asn 530 - # 535 - # 540 - - A - # - # - # 1633 - - - - (2) INFORMATION FOR SEQ ID NO: 9: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 544 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #9: - - Cys Thr Ile Lys Trp Gln Gln Thr Val Pro Se - #r Gly Val Trp Thr Glu 1 5 - # 10 - # 15 - - Val Ser Gly Ser Tyr Thr Val Pro Gln Thr Al - #a Thr Gln Leu Ile Phe 20 - # 25 - # 30 - - Tyr Val Glu Ser Pro Asn Ala Thr Leu Asp Ph - #e Tyr Leu Asp Asp Phe 35 - # 40 - # 45 - - Thr Val Ile Asp Lys Asn Pro Val Thr Ile Pr - #o Ala Ala Ala Lys Glu 50 - # 55 - # 60 - - Pro Glu Leu Glu Ile Pro Ser Leu Cys Gln Gl - #n Tyr Ser Gln Tyr Phe 65 - # 70 - # 75 - # 80 - - Ser Ile Gly Val Ala Ile Pro Tyr Arg Val Le - #u Gln Asn Pro Val Glu 85 - # 90 - # 95 - - Arg Ala Met Val Leu Lys His Phe Asn Ser Il - #e Thr Ala Glu Asn Glu 100 - # 105 - # 110 - - Met Lys Pro Asp Ala Ile Gln Arg Thr Glu Gl - #y Gln Phe Asn Phe Asp 115 - # 120 - # 125 - - Val Ala Asp Gln Tyr Val Asp Phe Ala Gln Se - #r Asn Asn Ile Gly Ile 130 - # 135 - # 140 - - Arg Gly His Thr Leu Val Trp His Gln Gln Th - #r Pro Asp Trp Phe Phe 145 1 - #50 1 - #55 1 -#60 - - Gln His Ser Asp Gly Ser Pro Leu Asp Pro As - #n Asn Ser Glu AspLys 165 - # 170 - # 175 - - Gln Leu Leu Arg Asn Arg Leu Lys Thr His Il - #e Gln Thr Leu Val Gly 180 - # 185 - # 190 - - Arg Tyr Ala Glu Lys Val Tyr Ala Trp Asp Va - #l Val Asn Glu Ala Ile 195 - # 200 - # 205 - - Asp Glu Asn Gln Pro Asp Gly Tyr Arg Arg Se - #r Glu Trp Tyr Arg Ile 210 - # 215 - # 220 - - Leu Gly Pro Thr Pro Glu Thr Gly Gly Ile Pr - #o Glu Tyr Ile Ile Leu 225 2 - #30 2 - #35 2 -#40 - - Ala Phe Gln Tyr Ala Arg Glu Ala Asp Pro As - #n Ala Lys Leu PheTyr 245 - # 250 - # 255 - - Asn Asp Tyr Ser Thr Glu Asn Pro Lys Lys Ar - #g Gln Phe Ile Tyr Asn 260 - # 265 - # 270 - - Met Val Lys Ala Leu His Asp Arg Gly Leu Il - #e Asp Gly Val Gly Leu 275 - # 280 - # 285 - - Gln Gly His Ile Asn Val Asp Ser Pro Ala Va - #l Lys Glu Ile Glu Asp 290 - # 295 - # 300 - - Thr Ile Asn Leu Phe Ser Thr Ile Pro Gly Le - #u Gln Ile Gln Ile Thr 305 3 - #10 3 - #15 3 -#20 - - Glu Leu Asp Ile Ser Val Tyr Thr Ser Ser Th - #r Gln Gln Tyr AspThr 325 - # 330 - # 335 - - Leu Pro Gln Asp Ile Met Ile Lys Gln Ala Le - #u Lys Phe Lys Glu Leu 340 - # 345 - # 350 - - Phe Glu Met Leu Lys Arg His Ser Asp Arg Il - #e Thr Asn Val Thr Leu 355 - # 360 - # 365 - - Trp Gly Leu Lys Asp Asp Tyr Pro Trp Leu Se - #r Lys Asp Arg Ser Asn 370 - # 375 - # 380 - - Trp Pro Leu Leu Phe Asp Ser Asn Tyr Gln Al - #a Lys Tyr Asn Tyr Trp 385 3 - #90 3 - #95 4 -#00 - - Ala Ile Val Glu Pro Ser Val Leu Pro Val Al - #a Ile Asn Lys GlyTyr 405 - # 410 - # 415 - - Ala Asn Asn Ala Gln Pro Arg Ile Asp Gly Il - #e Met Asp Lys Glu Tyr 420 - # 425 - # 430 - - Lys Gly Thr Ile Pro Leu Ser Val Leu Asn As - #p Ala Gly Gln Asp Ile 435 - # 440 - # 445 - - Ala Gln Val Arg Ala Leu Trp Ser Gly Asn Gl - #u Leu Cys Leu Tyr Val 450 - # 455 - # 460 - - Thr Val Asn Asp Ser Ser Val Asp Ala Asn As - #n Asp Arg Val Val Ile 465 4 - #70 4 - #75 4 -#80 - - Phe Ile Asp Gln Asp Asn Gly Lys Leu Pro Gl - #u Leu Lys Asp AspAsp 485 - # 490 - # 495 - - Phe Trp Val Ser Ile Ser Arg Asn Gly Thr Ly - #s Asn Gln Ser Lys Thr 500 - # 505 - # 510 - - Gly Tyr Val Lys Asp Tyr Val Val Leu Gln Gl - #n Leu Asn Gly Tyr Thr 515 - # 520 - # 525 - - Met Glu Val Lys Leu Leu Leu Asn Asn Ser Le - #u Ala Ile Asn Thr Asn 530 - # 535 - # 540 - - - - (2) INFORMATION FOR SEQ ID NO: 10: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1125 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (A) ORGANISM: Extremophile (C) INDIVIDUAL ISOLATE: - #TG456 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..1125 (D) OTHER INFORMATION: - #/partial /product=- # "xylanase C" /gene= - #"xynC" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #10: - - CGC GAG TTA TTA CTT TAT GTT GAG GCG CAA AA - #T GCA AAT TTG GCT TTC 48 Arg Glu Leu Leu Leu Tyr Val Glu Ala Gln As - #n Ala Asn Leu Ala Phe 1 5 - # 10 - # 15 - - TGG GTT GAT GAT TTA AAG ATT TAT GAT TTA TC - #C AAG CTG GCT GAA CCT 96 Trp Val Asp Asp Leu Lys Ile Tyr Asp Leu Se - #r Lys Leu Ala Glu Pro 20 - # 25 - # 30 - - GAA TGG GAG ATA CCA TCT TTG ATA GAA AAG TA - #T AAA GAT TAT TTC AAA 144 Glu Trp Glu Ile Pro Ser Leu Ile Glu Lys Ty - #r Lys Asp Tyr Phe Lys 35 - # 40 - # 45 - - GTA GGG GTA GCT TTG TCT TAC AAA AGC ATT GC - #T YCT GAT ACA GAG AAG 192 Val Gly Val Ala Leu Ser Tyr Lys Ser Ile Al - #a Xaa Asp Thr Glu Lys 50 - # 55 - # 60 - - AAG ATG GTT TTG AAG CAT TTC AAT AGT ATT AC - #T GCA GGG AAT GAA ATG 240 Lys Met Val Leu Lys His Phe Asn Ser Ile Th - #r Ala Gly Asn Glu Met 65 - # 70 - # 75 - # 80 - - AAA CCA TCA GAG TTA CTT ATC AGT GAA AAT AA - #T TAT AAC TTT AGT AAA 288 Lys Pro Ser Glu Leu Leu Ile Ser Glu Asn As - #n Tyr Asn Phe Ser Lys 85 - # 90 - # 95 - - GCA GAT GAA TTT GTA AAT TTT GCA ACA AGT AA - #C AAC ATT GCC ATC AGA 336 Ala Asp Glu Phe Val Asn Phe Ala Thr Ser As - #n Asn Ile Ala Ile Arg 100 - # 105 - # 110 - - GGT CAT ACA CTG GTT TGG CAT GAG CAA ACA CC - #C GAC TGG TTT TTC AAG 384 Gly His Thr Leu Val Trp His Glu Gln Thr Pr - #o Asp Trp Phe Phe Lys 115 - # 120 - # 125 - - GAT GCA AAT GGA AAT ACC TTG AGC AAG GAT GC - #A TTG CTA AGC AGA TTA 432 Asp Ala Asn Gly Asn Thr Leu Ser Lys Asp Al - #a Leu Leu Ser Arg Leu 130 - # 135 - # 140 - - AAG CAG TAT ATT TAT ACG GTA GTG GGA AGA TA - #T AAA GGG AAG GTT TAT 480 Lys Gln Tyr Ile Tyr Thr Val Val Gly Arg Ty - #r Lys Gly Lys Val Tyr 145 1 - #50 1 - #55 1 -#60 - - GCA TGG GAT GTG GTA AAT RAA GCA ATA GAT GA - #A AGT CAA GGT AATGGA 528 Ala Trp Asp Val Val Asn Xaa Ala Ile Asp Gl - #u Ser Gln Gly Asn Gly 165 - # 170 - # 175 - - TTC AGG AGA TCT AAC TGG TAC AAC ATT TGT GG - #T CCC GAA TAT ATT GAA 576 Phe Arg Arg Ser Asn Trp Tyr Asn Ile Cys Gl - #y Pro Glu Tyr Ile Glu 180 - # 185 - # 190 - - AAG GCT TTT ATA TGG GCA CAT GAR GCC GAT CC - #A GAC GCA AAA TTG TTT 624 Lys Ala Phe Ile Trp Ala His Glu Ala Asp Pr - #o Asp Ala Lys Leu Phe 195 - # 200 - # 205 - - TAC AAC GAT TAC AAC ACA GAA AAC AGT CAG AA - #G AGA CAG TTT ATT TMC 672 Tyr Asn Asp Tyr Asn Thr Glu Asn Ser Gln Ly - #s Arg Gln Phe Ile Xaa 210 - # 215 - # 220 - - AAC ATG ATT AAG AGT CTC AAG GAA AAA GGT GT - #T CCA ATT CAT GGA ATA 720 Asn Met Ile Lys Ser Leu Lys Glu Lys Gly Va - #l Pro Ile His Gly Ile 225 2 - #30 2 - #35 2 -#40 - - GGA TTG CGG TGT CAT ATA AAT CTT GAT TGG CC - #C TCG ATT AGC GAGATA 768 Gly Leu Arg Cys His Ile Asn Leu Asp Trp Pr - #o Ser Ile Ser Glu Ile 245 - # 250 - # 255 - - GAG AAC ACC ATA AAA TTG TTC AGC TCT ATA CC - #T GGA TTG GAG ATA CAC 816 Glu Asn Thr Ile Lys Leu Phe Ser Ser Ile Pr - #o Gly Leu Glu Ile His 260 - # 265 - # 270 - - ATT ACG GAG CTT GAT ATG AGT TTT TAT CAG TG - #G GGT TCG AGT ACC AGT 864 Ile Thr Glu Leu Asp Met Ser Phe Tyr Gln Tr - #p Gly Ser Ser Thr Ser 275 - # 280 - # 285 - - TAT TCA ACG CCA CCM AGA GAT CTC CTG ATA AA - #A CAG GCA ATG AGA TAT 912 Tyr Ser Thr Pro Pro Arg Asp Leu Leu Ile Ly - #s Gln Ala Met Arg Tyr 290 - # 295 - # 300 - - AAG GAG TTA TTC GAT TTA TTT AAA AAG TAC AA - #T GTA ATA ACT AAT GTA 960 Lys Glu Leu Phe Asp Leu Phe Lys Lys Tyr As - #n Val Ile Thr Asn Val 305 3 - #10 3 - #15 3 -#20 - - ACA TTC TGG GGA CTA AAG GAT GAT TAC TCA TG - #G CTG AGT CAA AACTTT 1008 Thr Phe Trp Gly Leu Lys Asp Asp Tyr Ser Tr - #p Leu Ser Gln Asn Phe 325 - # 330 - # 335 - - GGA AAA AGT GAT TAC CCG TTG TTA TTT GAT GG - #A AAC TAT AAG TCA AAA 1056 Gly Lys Ser Asp Tyr Pro Leu Leu Phe Asp Gl - #y Asn Tyr Lys Ser Lys 340 - # 345 - # 350 - - TAT GCC TTT TGG AGC CTG ATT GAG CCA ACT GT - #G GTG CCG GTT ACC GGT 1104 Tyr Ala Phe Trp Ser Leu Ile Glu Pro Thr Va - #l Val Pro Val Thr Gly 355 - # 360 - # 365 - - CAT AGC TGT TTT TGC GCC ATG - # - # 1125 His Ser Cys Phe Cys Ala Met 370 - # 375 - - - - (2) INFORMATION FOR SEQ ID NO: 11: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 375 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #11: - - Arg Glu Leu Leu Leu Tyr Val Glu Ala Gln As - #n Ala Asn Leu Ala Phe 1 5 - # 10 - # 15 - - Trp Val Asp Asp Leu Lys Ile Tyr Asp Leu Se - #r Lys Leu Ala Glu Pro 20 - # 25 - # 30 - - Glu Trp Glu Ile Pro Ser Leu Ile Glu Lys Ty - #r Lys Asp Tyr Phe Lys 35 - # 40 - # 45 - - Val Gly Val Ala Leu Ser Tyr Lys Ser Ile Al - #a Xaa Asp Thr Glu Lys 50 - # 55 - # 60 - - Lys Met Val Leu Lys His Phe Asn Ser Ile Th - #r Ala Gly Asn Glu Met 65 - # 70 - # 75 - # 80 - - Lys Pro Ser Glu Leu Leu Ile Ser Glu Asn As - #n Tyr Asn Phe Ser Lys 85 - # 90 - # 95 - - Ala Asp Glu Phe Val Asn Phe Ala Thr Ser As - #n Asn Ile Ala Ile Arg 100 - # 105 - # 110 - - Gly His Thr Leu Val Trp His Glu Gln Thr Pr - #o Asp Trp Phe Phe Lys 115 - # 120 - # 125 - - Asp Ala Asn Gly Asn Thr Leu Ser Lys Asp Al - #a Leu Leu Ser Arg Leu 130 - # 135 - # 140 - - Lys Gln Tyr Ile Tyr Thr Val Val Gly Arg Ty - #r Lys Gly Lys Val Tyr 145 1 - #50 1 - #55 1 -#60 - - Ala Trp Asp Val Val Asn Xaa Ala Ile Asp Gl - #u Ser Gln Gly AsnGly 165 - # 170 - # 175 - - Phe Arg Arg Ser Asn Trp Tyr Asn Ile Cys Gl - #y Pro Glu Tyr Ile Glu 180 - # 185 - # 190 - - Lys Ala Phe Ile Trp Ala His Glu Ala Asp Pr - #o Asp Ala Lys Leu Phe 195 - # 200 - # 205 - - Tyr Asn Asp Tyr Asn Thr Glu Asn Ser Gln Ly - #s Arg Gln Phe Ile Xaa 210 - # 215 - # 220 - - Asn Met Ile Lys Ser Leu Lys Glu Lys Gly Va - #l Pro Ile His Gly Ile 225 2 - #30 2 - #35 2 -#40 - - Gly Leu Arg Cys His Ile Asn Leu Asp Trp Pr - #o Ser Ile Ser GluIle 245 - # 250 - # 255 - - Glu Asn Thr Ile Lys Leu Phe Ser Ser Ile Pr - #o Gly Leu Glu Ile His 260 - # 265 - # 270 - - Ile Thr Glu Leu Asp Met Ser Phe Tyr Gln Tr - #p Gly Ser Ser Thr Ser 275 - # 280 - # 285 - - Tyr Ser Thr Pro Pro Arg Asp Leu Leu Ile Ly - #s Gln Ala Met Arg Tyr 290 - # 295 - # 300 - - Lys Glu Leu Phe Asp Leu Phe Lys Lys Tyr As - #n Val Ile Thr Asn Val 305 3 - #10 3 - #15 3 -#20 - - Thr Phe Trp Gly Leu Lys Asp Asp Tyr Ser Tr - #p Leu Ser Gln AsnPhe 325 - # 330 - # 335 - - Gly Lys Ser Asp Tyr Pro Leu Leu Phe Asp Gl - #y Asn Tyr Lys Ser Lys 340 - # 345 - # 350 - - Tyr Ala Phe Trp Ser Leu Ile Glu Pro Thr Va - #l Val Pro Val Thr Gly 355 - # 360 - # 365 - - His Ser Cys Phe Cys Ala Met 370 - # 375 - - - - (2) INFORMATION FOR SEQ ID NO: 12: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1244 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: DNA (genomic) - - (iii) HYPOTHETICAL: NO - - (iii) ANTI-SENSE: NO - - (vi) ORIGINAL SOURCE: (A) ORGANISM: Extremophile (C) INDIVIDUAL ISOLATE: - #TG456 - - (ix) FEATURE: (A) NAME/KEY: CDS (B) LOCATION: 1..1107 (D) OTHER INFORMATION: - #/partial /product=- # "xylanase D" /gene= - #"xynD" - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #12: - - AAA GTC TTG CTG GCT GCT CTG ATG TGT GTT GT - #G TTG GCT AAT CCT TTT 48 Lys Val Leu Leu Ala Ala Leu Met Cys Val Va - #l Leu Ala Asn Pro Phe 1 5 - # 10 - # 15 - - TAT GCA CAG GCA GCC ATG ACA TTT ACC TCT AA - #T GCA ACT GGG ACA TAC 96 Tyr Ala Gln Ala Ala Met Thr Phe Thr Ser As - #n Ala Thr Gly Thr Tyr 20 - # 25 - # 30 - - GAT GGT TAC TAC TAC GAG TTG TGG AAG GAC AC - #A GGG AAT ACT ACC ATG 144 Asp Gly Tyr Tyr Tyr Glu Leu Trp Lys Asp Th - #r Gly Asn Thr Thr Met 35 - # 40 - # 45 - - ACA GTT GAC ACA GGA GGA AGA TTT AGC TGT CA - #G TGG AGT AAC ATT AAC 192 Thr Val Asp Thr Gly Gly Arg Phe Ser Cys Gl - #n Trp Ser Asn Ile Asn 50 - # 55 - # 60 - - AAT GCA CTC TTC AGA ACA GGT AAA AAG TTT AG - #C ACT GCA TGG AAT CAG 240 Asn Ala Leu Phe Arg Thr Gly Lys Lys Phe Se - #r Thr Ala Trp Asn Gln 65 - # 70 - # 75 - # 80 - - CTT GGG ACT GTA AAG ATT ACC TAC TCT GCT AC - #C TAC AAT CCA AAT GGC 288 Leu Gly Thr Val Lys Ile Thr Tyr Ser Ala Th - #r Tyr Asn Pro Asn Gly 85 - # 90 - # 95 - - AAT TCC TAT CTC TGC ATT TAT GGA TGG TCA AG - #A AAT CCA CTT GTT GAA 336 Asn Ser Tyr Leu Cys Ile Tyr Gly Trp Ser Ar - #g Asn Pro Leu Val Glu 100 - # 105 - # 110 - - TTT TAT ATC GTT GAA AGC TGG GGC TCA TGG CG - #T CCG CCC GGG GCA ACG 384 Phe Tyr Ile Val Glu Ser Trp Gly Ser Trp Ar - #g Pro Pro Gly Ala Thr 115 - # 120 - # 125 - - TCA CTT GGC ACT GTA ACA ATT GAT GGA GCA AC - #A TAT GAT ATT TAT AAG 432 Ser Leu Gly Thr Val Thr Ile Asp Gly Ala Th - #r Tyr Asp Ile Tyr Lys 130 - # 135 - # 140 - - ACA ACT CGT GTT AAT CAG CCA TCT ATC GAA GG - #A ACA AGA ACA TTT GAT 480 Thr Thr Arg Val Asn Gln Pro Ser Ile Glu Gl - #y Thr Arg Thr Phe Asp 145 1 - #50 1 - #55 1 -#60 - - CAG TAC TGG AGT GTT AGG ACA TCA AAG AGA AC - #A AGT GGT ACT GTTACT 528 Gln Tyr Trp Ser Val Arg Thr Ser Lys Arg Th - #r Ser Gly Thr Val Thr 165 - # 170 - # 175 - - GTA ACT GAT CAT TTC AAA GCA TGG GCT GCA AA - #A GGT TTG AAC CTG GGT 576 Val Thr Asp His Phe Lys Ala Trp Ala Ala Ly - #s Gly Leu Asn Leu Gly 180 - # 185 - # 190 - - ACA ATT GAC CAG ATT ACA CTC TGT GTG GAA GG - #Y TAC CAR AGC AGC GGC 624 Thr Ile Asp Gln Ile Thr Leu Cys Val Glu Gl - #y Tyr Gln Ser Ser Gly 195 - # 200 - # 205 - - TCA GCA AAT ATA ACA CAG AAT ACA TTT ACT AT - #T GGT GGT TCG AGT AGT 672 Ser Ala Asn Ile Thr Gln Asn Thr Phe Thr Il - #e Gly Gly Ser Ser Ser 210 - # 215 - # 220 - - GGC TCA AGT AAT GGT TCA AAT AAC GGT TCA AA - #T GAT GGT TCC AAT GGA 720 Gly Ser Ser Asn Gly Ser Asn Asn Gly Ser As - #n Asp Gly Ser Asn Gly 225 2 - #30 2 - #35 2 -#40 - - GGA ACA AAT GCA GGA ATT TCA ACY GCA AGC AG - #G ATA GAA TGT GAAAGT 768 Gly Thr Asn Ala Gly Ile Ser Thr Ala Ser Ar - #g Ile Glu Cys Glu Ser 245 - # 250 - # 255 - - ATG TCG CTC AGC GGY CCT TAT GTT TCA AGA AT - #T ACT TAT CCA TTT AAT 816 Met Ser Leu Ser Gly Pro Tyr Val Ser Arg Il - #e Thr Tyr Pro Phe Asn 260 - # 265 - # 270 - - GGT ATA GCA CTT TAT GCG AAC GGA GAT AGA GC - #A ACG GCA AAT GTA AAC 864 Gly Ile Ala Leu Tyr Ala Asn Gly Asp Arg Al - #a Thr Ala Asn Val Asn 275 - # 280 - # 285 - - TTT TCA GCA AGC CGT AAC TAT ACT TTT AAA TT - #A CGT GGA TGT GGA AAT 912 Phe Ser Ala Ser Arg Asn Tyr Thr Phe Lys Le - #u Arg Gly Cys Gly Asn 290 - # 295 - # 300 - - AAC AAT AAT TTG GCA TCA GTT GAT TTA CTG AT - #A GAT GGA AAG AAA GTA 960 Asn Asn Asn Leu Ala Ser Val Asp Leu Leu Il - #e Asp Gly Lys Lys Val 305 3 - #10 3 - #15 3 -#20 - - GGT TCG TTC TAT TAT AAG GGA ACA TAT CCT TG - #G GAA GCY TCT ATAAAT 1008 Gly Ser Phe Tyr Tyr Lys Gly Thr Tyr Pro Tr - #p Glu Ala Ser Ile Asn 325 - # 330 - # 335 - - AAT GTG TAT GTA AGT GCA GGT ACC CAC AGA GW - #G GAG CTT GTA CTT TCT 1056 Asn Val Tyr Val Ser Ala Gly Thr His Arg Xa - #a Glu Leu Val Leu Ser 340 - # 345 - # 350 - - GCT GAT AAT GGT ACA TGG GAT GTC TAT GCG GA - #T TAT TTG TTA ATA CAA 1104 Ala Asp Asn Gly Thr Trp Asp Val Tyr Ala As - #p Tyr Leu Leu Ile Gln 355 - # 360 - # 365 - - TGAAATTCGG AAATGTTTTT AAAAATACTG CTTCGRAGAA GCAGGTATTT TT -#TTATGTTC 1164 - - ACTATTATAA AGCGATTGAA GTCAGTCTTA GTTCATCCTA GTTGTTCTTC AR -#ACCGRTCA 1224 - - TAGCTGTTTC CKGCGCCATG - # - # 124 - #4 - - - - (2) INFORMATION FOR SEQ ID NO: 13: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 368 amino - #acids (B) TYPE: amino acid (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: protein - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #13: - - Lys Val Leu Leu Ala Ala Leu Met Cys Val Va - #l Leu Ala Asn Pro Phe 1 5 - # 10 - # 15 - - Tyr Ala Gln Ala Ala Met Thr Phe Thr Ser As - #n Ala Thr Gly Thr Tyr 20 - # 25 - # 30 - - Asp Gly Tyr Tyr Tyr Glu Leu Trp Lys Asp Th - #r Gly Asn Thr Thr Met 35 - # 40 - # 45 - - Thr Val Asp Thr Gly Gly Arg Phe Ser Cys Gl - #n Trp Ser Asn Ile Asn 50 - # 55 - # 60 - - Asn Ala Leu Phe Arg Thr Gly Lys Lys Phe Se - #r Thr Ala Trp Asn Gln 65 - # 70 - # 75 - # 80 - - Leu Gly Thr Val Lys Ile Thr Tyr Ser Ala Th - #r Tyr Asn Pro Asn Gly 85 - # 90 - # 95 - - Asn Ser Tyr Leu Cys Ile Tyr Gly Trp Ser Ar - #g Asn Pro Leu Val Glu 100 - # 105 - # 110 - - Phe Tyr Ile Val Glu Ser Trp Gly Ser Trp Ar - #g Pro Pro Gly Ala Thr 115 - # 120 - # 125 - - Ser Leu Gly Thr Val Thr Ile Asp Gly Ala Th - #r Tyr Asp Ile Tyr Lys 130 - # 135 - # 140 - - Thr Thr Arg Val Asn Gln Pro Ser Ile Glu Gl - #y Thr Arg Thr Phe Asp 145 1 - #50 1 - #55 1 -#60 - - Gln Tyr Trp Ser Val Arg Thr Ser Lys Arg Th - #r Ser Gly Thr ValThr 165 - # 170 - # 175 - - Val Thr Asp His Phe Lys Ala Trp Ala Ala Ly - #s Gly Leu Asn Leu Gly 180 - # 185 - # 190 - - Thr Ile Asp Gln Ile Thr Leu Cys Val Glu Gl - #y Tyr Gln Ser Ser Gly 195 - # 200 - # 205 - - Ser Ala Asn Ile Thr Gln Asn Thr Phe Thr Il - #e Gly Gly Ser Ser Ser 210 - # 215 - # 220 - - Gly Ser Ser Asn Gly Ser Asn Asn Gly Ser As - #n Asp Gly Ser Asn Gly 225 2 - #30 2 - #35 2 -#40 - - Gly Thr Asn Ala Gly Ile Ser Thr Ala Ser Ar - #g Ile Glu Cys GluSer 245 - # 250 - # 255 - - Met Ser Leu Ser Gly Pro Tyr Val Ser Arg Il - #e Thr Tyr Pro Phe Asn 260 - # 265 - # 270 - - Gly Ile Ala Leu Tyr Ala Asn Gly Asp Arg Al - #a Thr Ala Asn Val Asn 275 - # 280 - # 285 - - Phe Ser Ala Ser Arg Asn Tyr Thr Phe Lys Le - #u Arg Gly Cys Gly Asn 290 - # 295 - # 300 - - Asn Asn Asn Leu Ala Ser Val Asp Leu Leu Il - #e Asp Gly Lys Lys Val 305 3 - #10 3 - #15 3 -#20 - - Gly Ser Phe Tyr Tyr Lys Gly Thr Tyr Pro Tr - #p Glu Ala Ser IleAsn 325 - # 330 - # 335 - - Asn Val Tyr Val Ser Ala Gly Thr His Arg Xa - #a Glu Leu Val Leu Ser 340 - # 345 - # 350 - - Ala Asp Asn Gly Thr Trp Asp Val Tyr Ala As - #p Tyr Leu Leu Ile Gln 355 - # 360 - # 365__________________________________________________________________________

Number	Date	Country
0 511 933 A2	Apr 1992	EPX
0 538 177 A1	Oct 1992	EPX
WO 9319171	Mar 1993	WOX
WO 9512668	Nov 1994	WOX

Thermostable xylanases

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Foreign Referenced Citations (4)

Non-Patent Literature Citations (4)

Entry
Ruttersmith, R.M., et al., Cellulolytic and Hemicellulolytic Enzymes Functional Above 100.degree.C; Annals of NY Acad. of Sci., pp. 137-141, vol. 672 (Enzyme Engineering XI), (1992).
Sakka, K., et al., Nucleotide Sequence of the Clostridium stercorarium xynA Gene Encoding Xylanase A: Identification of Catalytic and Cellulose Binding Domains; Biosci, Biotech. Biochem. (1993) 57:273-277.
Sakka, K. et al., Cloning and Expression in Escherichia coli of Clostridium stercorarium Strain F-9 Genes Related to Xylan Hydrolysis, Agric. Biol. Chem. (1990), 54:337-342.
Irwin, D., Characterization and Sequence of a Thermomonospora fusca Xylanase, App. Envir. Micro. (1994) p. 763-770.