Gene for enzyme having both alkaline pullulanase and alkaline α-amylase activities

Abstract

The present invention provides a DNA fragment encoding alkaline pullulanase exhibiting alkaline α-amylase activity, alkaline α-amylase possessing both an amino acid sequence described in SEQ ID NO:3 and a DNA fragment encoding the amylase, alkaline pullulanase possessing both an amino acid sequence described in SEQ ID NO:4 and a DNA fragment encoding the pullulanase, recombinant DNAs containing these DNA fragments, and transformed microorganisms harboring the recombinant DNAs. The technique of the present invention enables mass production of alkaline pullulanase exhibiting alkaline α-amylase activity.

Description

TECHNICAL FIELD

The present invention relates to the gene encoding an enzyme that exhibits both alkaline pullulanase activity and alkaline α-amylase activity (alkaline amylopullulanase), to alkaline α-amylase and alkaline pullulanase obtainable from expression of a fragment of the gene encoding the intact alkaline amylopullulanase, to the gene or fragments thereof encoding these enzymatic activities, and to recombinant DNAs and transformants bearing the gene and fragments thereof.

BACKGROUND ART

Alpha-amylase has long been used in a variety of fields. For example, it has been used for the saccharification of grains and potatoes in the fermentation industry, as starch paste removers in the textile industry, as digestives in the pharmaceutical industry, and for the manufacture of thick malt sugar syrups in the food industry. Alpha-amylase is an enzyme which acts on starch-related polysaccharides such as amylose or amylopectin, cutting solely the α-1,4-glucoside bond of the polysaccharide molecule. Crystalline samples or electrophoretically uniform samples of α-amylase have been obtained from a number of different sources including bacteria, fungi, plant seeds, and animal digestive glands. Pullulanase is an enzyme which hydrolyzes solely the α-1,6-glucoside bond present in starch, glycogen, amylopectin, and pullulan. Pullulanase was first found in a certain strain of Aerobacter aerogenes (Bender, H. and Wallenfels, K., Biochem . J., 334, 79 (1961)), and thereafter, was also found in many other microorganisms including genera Bacillus, Streptococcus and Clostridium. Pullulanase has become of interest in the starch-making industry because of its ability to produce, from starch, maltooligosaccharides such as glucose, maltose, maltotriose, maltopentaose, and maltohexaose when it is used in combination with endo-type amylase and exo-type amylase.

In order to simplify the process of the manufacture of saccharides in which two or more enzymes are used, as described above, pullulanase which also acts on the α-1,4-glucoside bond, in other words, pullulanase exhibiting α-amylase activity, is greatly desired. Bacillus subtilis TU strain is known to produce a pullulanase-amylase complex enzyme (Takasaki, Y., Agric. Biol. Chem., 51, 9 (1987), Japanese Patent Publication (kokoku) No. 1-18717). In addition, enzymes exhibiting the above two distinct enzymatic activities or so-called amylopullulanases have been reported for a number of bacteria including Bacillus circulans (Japanese Patent Application Laid-open (kokai) No. 64-60376), Bacillus sp. (Saha, B. C., et al., Enzyme Microb. Technol., 11, 760 (1989)), Thermoanaerobium brockii (Coleman, R. D. et al., J. Bacteriol., 169, 4302 (1987)), Thermoanaerobium sp. (Plant, A. R., et al., Appl. Microbiol. Biotechnol., 26, 427 (1987)), Clostridium thermohydrosulfuricum (Saha, B. C., et al., Biochem. J., 252, 343 (1988)), Clostridium thermosulfurogenes (Spreinat, A. et al., Appl. Microbiol. Biotechnol., 33, 511 (1990)), Thermus aquaticus (Plant, A. R., et al., Enzyme Microb. Technol., 8, 668 (1986)), Thermus sp. (Nakamura, N et al., Starch/Starke, 41, 112 (1989)), Thermoanaerobacterium saccharolyticum (Saha, B. C., et al., Appl. Environ. Microbiol., 56, 881 (1990)), and Pyrococcus furiosus and Thermococcus litoralis (Brown, S. H. and Kelley, R. M., Appl. Environ. Microbiol., 59, 2614 (1993)).

The present inventors have recently discovered that the efficacy of dish-washing detergents and detergents for clothes can be greatly improved, particularly on starch soils, when α-amylase and pullulanase are both incorporated into the detergents (Japanese Patent Application Laid-open (Kokai) No. 2-132193). However, most of the α-amylases and pullulanases previously found in the natural world exhibit maximal and stable enzymatic activities in the neutral to acidic pH ranges, but scarcely work in an alkaline solution of pH 9-10. There exist very few enzymes exhibiting maximal activities in the alkaline pH range (alkaline pullulanases), and only two reports of such enzymes have been published (Nakamura, N. and Horikoshi, K., Biochim. Bophys. Acta, 397, 188 (1975), Japanese Patent Publication (kokoku) No. 53-27786 and Ara et al. Japanese Patent Publication kokoku) No. 6-32613. Furthermore, an enzyme that has both alkaline α-amylase and alkaline pullulanase activities had not been reported until the present inventors discovered that an alkalophilic Bacillus sp. KSM-AP1378 (FERM BP-3048, deposited Jul. 24, 1989 in Fermentation Research Institute, Agency of Industrial Science and Technology of 1-3, Higashi 1-chome, Tsukuba-shi, Ibaraki, 305 Japan) having its optimum pH for growth in the alkaline range produces a novel alkaline amylopullulanase (formerly designated pullulanase Y) that has both alkaline pullulanase and alkaline α-amylase activities. They elucidated that this enzyme is useful as an additive in detergent compositions for automatic dishwashers and in detergent compositions for clothes (Japanese Patent Application Laid-open (kokai) No. 3-290498). Although this enzyme is constituted by a single enzyme molecule, it exhibits both alkaline α-amylase activity and alkaline pullulanase activity. Exploitation of this enzyme has proved very advantageous in culturing the bacteria and in purification of the enzyme, compared to the case in which the two enzymes are independently produced by two different bacteria.

The present inventors have attempted to improve productivity of the alkaline amylopullulanase (formerly designated pullulanase Y) producing bacterium, Bacillus sp. KSM-AP1378, through optimization of culturing methods. Nevertheless, it is still desired to improve further the enzyme productivity of the bacterium so as to advantageously produce the alkaline amylopullulanase on an industrial scale. It is noted that production of the enzyme can be further enhanced using genetic engineering and the activity of the enzyme itself can be improved by altering the gene encoding the enzyme using a protein engineering approach. Applying these approaches requires the gene encoding alkaline amylopullulanase.

Accordingly, an object of the present invention is to provide the gene encoding alkaline amylopullulanase, recombinant DNA comprising the gene, and a transformant harboring the recombinant DNA.

The DNA encoding the alkaline amylopullulanase gene may be further used to produce probes to be used in the isolation of additional, homologous alkaline amylopullulanase genes from other microorganisms. Thus, an additional object of the present invention is to provide a means of screening for and isolating additional alkaline amylopullulanase enzymes.

DISCLOSURE OF THE INVENTION

The present inventors isolated a DNA fragment encoding alkaline amylopullulanase from the chromosomal DNA of an alkalophilic Bacillus strain using shotgun cloning and PCR. When they transformed a microorganism with this DNA fragment ligated to a suitable vector, it was confirmed that the resultant recombinant microorganism produced alkaline amylopullulanase. Moreover, it was found that the amino acid sequence of the alkaline amylopullulanase encoded by the DNA fragment is completely different from those of previously known amylases and pullulanases, and that this enzyme has the feature that the amino terminal moiety of the enzyme molecule is alkaline α-amylase, and the carboxy terminal moiety of the enzyme molecule is alkaline pullulanase. The present invention was accomplished based on this finding.

Accordingly, the present invention provides a DNA fragment encoding alkaline amylopullulanase.

The present invention also provides alkaline α-amylase having the amino acid sequence described in SEQ ID NO:3 provided hereinbelow, as well as a DNA fragment encoding the alkaline α-amylase.

The present invention also provides alkaline pullulanase having the amino acid sequence described in SEQ ID NO:4 provided hereinbelow, as well as a DNA fragment encoding the alkaline pullulanase.

The present invention also provides recombinant DNA comprising a DNA fragment encoding the above-described alkaline amylopullulanase, alkaline α-amylase, or alkaline pullulanase.

The present invention also provides a transformed microorganism harboring recombinant DNA comprising a DNA fragment encoding the above-described alkaline amylopullulanase, alkaline α-amylase, or alkaline pullulanase.

The present invention further provides a method for producing alkaline amylopullulanase, alkaline α-amylase, or alkaline pullulanase, characterized by culturing the above-described transformed microorganism and collecting any one of the expressed enzymes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a restriction enzyme map of the alkaline amylopullulanase gene from Bacillus sp. KSM-AP1378 and positions of the primers.

FIG. 2 is a scheme of subcloning of the alkaline amylopullulanase gene from Bacillus sp. KSM-AP1378.

FIG. 3 is a graph showing the pH profiles of α-amylase activity and pullulanase activity of alkaline amylopullulanase.

FIG. 4 shows the result of Southern hybridization analysis of PstI digestion products of the chromosomal DNA of a strain KSM-AP1378 from Bacillus sp. KSM-AP1378 using fragment A as a probe. On the left-hand side of the Southern filter, the positions of a size marker for lambda DNA-HindIII digestion products (Boehringer Mannheim) which simultaneously underwent electrophoresis are indicated together with the sizes of the respective DNA fragments.

FIG. 5 shows the result of Southern hybridization analysis of XbaI digestion products of the chromosomal DNA of a strain KSM-AP1378 from Bacillus sp. KSM-AP1378 using fragment C as a probe. On the left-hand side of the Southern filter, the positions of a size marker for lambda DNA-HindIII digestion products (Boehringer Mannheim) which simultaneously underwent electrophoresis are indicated together with the sizes of the respective DNA fragments.

FIG. 6 shows nucleotide sequences of primers used for PCR (SEQ ID NO:7 to 14). Primers 1 (SEQ ID NO:7), 3 (SEQ ID NO:9), 5 (SEQ ID NO:10), and B (SEQ ID NO:14), were used as complementary sequences.

FIG. 7 shows the result of Southern hybridization analysis of EcoRI digestion products of the chromosomal DNA of a strain KSM-AP1378 from Bacillus sp. KSM-AP1378 using fragment D as a probe. On the left-hand side of the Southern filter, the positions of a size marker for lambda DNA-HindIII digestion products (Boehringer Mannheim) which simultaneously underwent electrophoresis are indicated together with the sizes of the respective DNA fragments.

FIG. 8 shows the result of Southern hybridization analysis of XbaI digestion products of the chromosomal DNA of a strain KSM-AP1378 from Bacillus sp. KSM-AP1378 using fragment E as a probe. On the left-hand side of the Southern filter, the positions of a size marker for lambda DNA-HindIII digestion products (Boehringer Mannheim) which simultaneously underwent electrophoresis are indicated together with the sizes of the respective DNA fragments.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

In the present invention, a useful microorganism which serves as an alkaline amylopullulanase gene donor may be, for example, Bacillus sp. KSM-AP1378, which is an alkalophilic Bacillus. This strain was isolated from the soil in the vicinity of the city of Tochigi in Tochigi Prefecture, Japan by the present inventors and identified as a strain producing significant amounts of alkaline amylopullulanase. This strain has,been deposited at the Fermentation Research Institute under BP-3048.

In order to obtain chromosomal DNA from a donor microorganism, methods proposed by Marmur, J. ( J. Mol. Biol., 3, 208 (1961)) and by Saito, H. and Miura, K. ( Biochim. Biophys. Acta, 72, 619 (1963)) may be used. Other similar methods may also be used.

DNA fragments comprising the alkaline amylopullulanase gene are prepared by cleaving the thus-obtained chromosomal DNA using restriction enzymes. Restriction enzymes which may be used are not particularly limited so long as they do not damage the gene. The alkaline amylopullulanase gene may also be obtained by PCR. For example, the gene may be obtained by synthesizing primers having sequences corresponding to those on the upstream side of the 5′-terminus and on the downstream side of the 3′-terminus of the essential region based on the nucleotide sequence described in SEQ ID NO:1, and conducting PCR using, as a template, the chromosomal DNA of an alkaline amylopullulanase-producing microorganism. Alternatively, an intact gene may be obtained by either method of first obtaining an alkaline pullulanase gene fragment from an alkaline amylopullulanase-producing microorganism using any procedure, followed by PCR which amplifies an alkaline α-amylase gene fragment existing on the upstream side of the former fragment, or conversely, via a method of first obtaining an alkaline α-amylase gene, followed by PCR which amplifies an alkaline pullulanase gene fragment existing on the downstream side of the gene.

The thus-prepared genetic fragment is then subjected to cloning. Host/vector systems which may be used are not particularly limited, so far as host bacterial strains express the alkaline amylopullulanase gene of the present invention, that the recombinant DNA can be replicated in the host bacteria, and that the recombinant DNA can stably harbor the integrated gene. For example, members of the EK system in which the host is E. coli K-12, and those of the BS system in which the host is Bacillus subtilis Marburg may be used. Use of the EK system which encompasses many kinds of vectors and is extensively studied genetically provides good results and thus is preferred. Specific examples of host bacteria include strains HB101, C600, and JM109 of the EK system, and strains BD170, MI11, and ISW1214 of the BS system. Specific examples of vectors include pBR322 and pUC18 of the EK system, and pUB110 and pHY300PLK of the BS system. A recombinant plasmid DNA is created by cleaving a vector with a restriction enzyme followed by ligation with the above-mentioned chromosomal or PCR-amplified DNA fragment. The ligation may be achieved, for example, through the use of a DNA ligase.

Methods for transforming host bacterial strains using recombinant DNA are not particularly limited. For example, a calcium chloride method (Mandel, M. and Higa, A., J. Mol. Biol., 53, 159 (1970)) may be used in the case of hosts of the EK system, and a protoplast method (Chang, C. and Cohen, S. N., Mol. Gen. Genet., 168, 111 (1978)) may be used in the case of hosts of the BS system.

Selection of recombinant microorganisms are performed as follows. First, microorganisms which have been transformed with DNA containing a vector-derived DNA fragment are selected using, as an index, a character such as antibiotics resistance coded on the vector DNA which is not inactivated by insertion of exogenous chromosomal or PCR-amplified DNA fragments. For example, in a specific case in which pBR322 of EK system is used as a vector, and a BamHI fragment of chromosomal DNA is inserted into the BamHI cleavage site of pBR322, the tetracycline resistant gene is inactivated, so a primary selection may be conducted using, as an index, ampicillin resistance without having a BamHI cleavage site in the gene. Subsequently, the selected microorganisms are transferred onto agar plates containing starch or pullulan using, for example, a replica method and are then cultured to form colonies. Colonies are detected that decompose starch, that form halos on the starch-containing agar plate, and that also form halos on the pullulan-containing agar plate.

The recombinant DNA harbored by the thus-obtained recombinant microorganism can be extracted using standard procedures for preparing plasmids or phage DNAs (Maniatis, T. et al., Molecular Cloning , Cold Spring Harbor Laboratory, New York (1982)). By cleaving the extracted recombinant DNA using a variety of restriction enzymes and analyzing cleavage patterns by electrophoresis, it is confirmed that the recombinant DNA is a ligated product of the vector DNA and a DNA fragment containing the alkaline amylopullulanase gene.

Fragments encoding the alkaline pullulanase activity, parts of the alkaline amylopullulanase of the present invention, are contained in a DNA fragment of about 9.4 kb, as shown in the restriction enzyme map of FIG. 1 , and are present in the segment of about 6.2 kb shown by the cross-hatched bar.

The fragment having a size of about 6.2 kb and containing the alkaline amylopullulanase gene has a nucleotide sequence shown by SEQ ID NO:2. In this sequence, the 5′ terminus and 3′terminus correspond to the left-hand side and the right-hand side, respectively, of the fragment of about 6.2 kb. In this sequence is observed an open reading frame (ORF) starting translation at the 145th ATG and coding for a sequence formed of 1938 amino acid residues described in SEQ ID NO:2. Fifteen bases (15b) upstream of the ORF, there exists a sequence GAAAGGGG which is highly complementary to the 3′ terminal sequence of the 16S ribosomal RNA of Bacillus subtilis (McLaughlin, J. R. et al., J. Biol. Chem., 256, 11283 (1981)). On a further upstream side extending from the 35th nucleotide, there exists a sequence TTTACA . . . 20 b . . . TAAATT which has high homology with the consensus sequence of a σ A -type promoter (Gitt, M. A. et al, J. Biol. Chem., 260, 7178 (1985)). On the downstream side of the translation termination codon TAA at the 5959th nucleotide, there exists an inverted repeated sequence (nucleotide Nos. 5961-6015) which is presumably a transcription terminator. In addition, the amino acid sequence of the 14 residues on the amino terminus side in alkaline amylopullulanase obtained through purifying a culture of Bacillus sp. KSM-AP1378 coincides with the sequence extending from the first amino acid (amino acids 1-14 in SEQ ID NO:2) deduced from the nucleotide sequence in the present DNA fragment.

When the nucleotide sequence of the gene of the present invention and a putative amino acid sequence were compared with those of α-amylase and pullulanase known hitherto, it was confirmed that the present gene is a novel one possessing a unique nucleotide sequence, with the amino acid sequence encoded by the gene being different from that of either α-amylase or pullulanase.

Moreover, the gene of the present invention is characterized in that it encodes an enzyme possessing two active centers, one for alkaline α-amylase and the other for alkaline pullulanase, in a single peptide chain of the protein. There is each of four sequences (regions I-IV; Nakajima, R. et al, Appl. Microbiol. Biotechnol., 23, 355 (1986)) observed uniquely for the active center of amylase, amino acids 430-613, and for pullulanase, amino acids 1364-1549. Specifically, in the amino acid sequence of SEQ ID NO:1, region I of alkaline α-amylase=430-435, region II of alkaline α-amylase=514-522, region III of alkaline α-amylase=547-550, region IV of alkaline α-amylase=608-613, region I of alkaline pullulanase=1364-1369, region II of alkaline pullulanase=1428-1436, region III of alkaline pullulanase=1461-1464, region IV of alkaline pullulanase 1544-1549. Moreover, between the structural genes presumably encoding alkaline α-amylase and alkaline pullulanase, respectively, an intervening sequence formed of 33 amino acids appears twice (in the amino acid of Sequence No. 2, 802-834 and 912-944). Therefore, by using the characteristic feature, it is also possible to express the alkaline α-amylase moiety and the alkaline pullulanase moiety in an independent manner. For example, if a gene encoding the amino acids stretching from the initiation codon to directly before the intervening sequence is inserted into a plasmid vector DNA and is introduced into a suitable host bacterium, it is possible to produce alkaline α-amylase alone (Sequence NO. 3). Likewise, if a gene containing the amino acids stretching directly after the intervening sequence to the 1906th amino acid is inserted into a plasmid vector DNA and is introduced into a suitable host bacterium, it is possible to produce alkaline pullulanase alone (SEQ ID NO:4).

An example of a preferred recombinant DNA containing the entire region of the alkaline amylopullulanase gene is plasmid pAP101 (FIG. 2 ). This plasmid has a size of 13.4 kb and is of a fragment containing the 6.2 kb alkaline amylopullulanase gene and part of pHY300PLK and pUC18. An example of a preferred recombinant microorganism harboring the recombinant DNA is an E. coli HB101(pAP101) strain. This strain is a product obtained by transforming E. coli HB101 strain with a recombinant plasmid, pAP101, using a standard transformation method. When this strain is cultured using a medium routinely employed for culturing E. coli , it produces alkaline amylopullulanase. The optimum reaction pHs of the thus-produced enzyme are pH 8-9 for the α-amylase activity and pH 9-10 for the pullulanase activity. This agrees well with the activity-pH relationship profiles determined for alkaline amylopullulanase produced by the gene donor bacterium Bacillus sp. KSM-AP1378 (FIG. 3 ).

The DNA fragments of the present invention are not necessarily limited only to those encoding the amino acid sequences shown in the below-described sequence listing so far as they encode a protein having the enzymatic activity of interest, and they encompass DNA fragments encoding an amino acid sequence in which one or more amino acids are substituted, added, deleted, inverted, or inserted. An example of such DNA is one encoding an amino acid sequence equivalent to the amino acid sequence described in SEQ ID NO:2 from which 32 amino acids on the N-terminal side have been deleted. Thus an alkaline amylopullulanase of SEQ ID NO:2 wherein between 1 to 32 amino acids have been deleted from the amino terminus is encompassed by the present invention.

When the thus-obtained transformants are cultured using known methods, alkaline α-amylase, alkaline pullulanase, or alkaline amylopullulanase can be produced. That is, if a transformant containing a domain encoding only alkaline α-amylase is used, alkaline α-amylase is obtained; if a transformant containing a domain encoding only alkaline pullulanase is used, alkaline pullulanase is obtained; and if a transformant containing a domain coding for the entire alkaline amylopullulanase is used, alkaline amylopullulanase is obtained.

The DNA fragments of the present invention may be further used as probes for the isolation of homologous alkaline amylopullulanase genes from other organisms.

EXAMPLES

The present invention will next be described in more detail by way of examples, which should not be construed as limiting the invention thereto. Concentrations in the Examples are all on a basis of % by weight.

Example 1

Isolation of Chromosomal DNA

Bacillus sp. KSM-AP1378 which produces alkaline amylopullulanase was inoculated into 5 ml of medium A (Table 1) and subjected to shaking culture at 30° C. for 24 hours. One ml of the culture was inoculated in 100 ml of the same medium, followed by shaking culture at 30° C. for a further 12 hours. Subsequently, cells were centrifugally collected and about 1 mg of chromosomal DNA was obtained in accordance with a method proposed by Saito and Miura (Saito, H. and Miura K., Biochim Biophys. Acta, 72, 619 (1963)).

TABLE 1
Composition of medium A
Pullulan                         1.0%
Tryptone                         0.2%
Yeast extract                    0.1%
KH                                                                        2                                                                    PO                                                                        4 0.03%
(NH                                                                        4                                                                    )                                                                        2                                                                    SO                                                                        4 0.1%
MgSO                                                                        4                                                                     · 7H                                                                        2                                                                    O 0.02%
CaCl                                                                        2                                                                     · 2H                                                                        2                                                                    O 0.02%
FeSO                                                                        4                                                                     · 7H                                                                        2                                                                    O 0.001%
MnCl                                                                        2                                                                     · 4H                                                                        2                                                                    O 0.0001%
Na                                                                        2                                                                    CO                                                                        3 0.5% (separately
                                 sterilized)
                                 pH: 10

Example 2

Isolation of DNA Fragment Encoding Alkaline Pullulanase

The chromosomal DNA (10 μg) obtained in Example 1 was cleaved using a restriction enzyme PstI, after which a vector plasmid pBR322 (1 μg, Boehringer Mannheim) which had been cleaved likewise with PstI was added and a ligation reaction was caused using T4 DNA ligase, thereby producing a mixture of recombinant plasmids. A suspension of E. coli which had undergone transformation with the recombinant plasmid mixture was spread onto an LB agar plate medium (1.0% tryptone (Difco), 0.5% yeast extract (Difco), 1.0% NaCl, and 1.5% agar (Wako Pure Chemical)) containing 15 μg/ml of tetracycline and cultured at 37° C. for 12 hours. On the colonies of transformed cells which emerged, 0.8% agar containing 0.2% pullulan, 0.8% red pullulan (Kanno, M. and Tomiura, E., Agric. Biol. Chem., 49, 1529 (1985)), 1 mg/ml of lysozyme, and a glycine-NaCl—NaOH buffer (pH 9.0) was overlaid and reaction was caused at 37° C. for 5 hours. As a result, a single strain was obtained which formed a transparent halo around a colony of the strain due to decomposition of red pullulan. This strain was isolated as a recombinant microorganism capable of producing alkaline pullulanase.

Example 3

Restriction Map of Plasmid With Alkaline Pullulanase DNA

The recombinant microorganism obtained in Example 2 was inoculated into 5 ml of an LB medium (1.0% tryptone (Difco), 0.5% yeast extract (Difco), 1.0% NaCl1) containing 15 μg/ml of tetracycline and cultured at 37° C. overnight. Thereafter, the culture was transferred into 500 ml of an LB medium, followed by shaking culture for 24 hours. Cells were centrifugally collected from the culture, and about 500 mg of a recombinant plasmid was obtained using a standard method (Maniatis, T. et al., Molecular Cloning , Cold Spring Harbor Laboratory (1982)). From a restriction enzyme map of the resultant recombinant plasmid, it was found that the plasmid contained a PstI fragment (fragment A) of about 6.3 kb, as shown in FIG. 1 . This plasmid was named pPU100. The E. coli HB101 strain transformed with the plasmid pPU100 was named HB100(pPU100).

Example 4

Measurement of Alkaline Pullulanase Activity

One ml of a culture of strain HB101(pPU100) which had been cultured overnight using 5 ml of an LB medium (containing tetracycline) was inoculated into 100 ml of an LB medium (containing tetracycline), followed by shaking culture at 37° C. for 24 hours. Subsequently, the cells collected through centrifugal separation were suspended in Tris-HCl buffer (pH 8.0) and the cells were disrupted by sonication. The cell debris was removed by centrifugal separation, and the supernatant was used as a cell-free extract. Similarly, a control cell-free extract was prepared using strain HB101(pBR322). Pullulanase activity of these extracts was measured. The pullulanase activity was measured by first causing a reaction in a reaction mixture containing 40 mM glycine-NaCl—NaOH buffer (pH 10) and pullulan (final concentration=0.25%) at 40° C. for 30 minutes, and the resultant reducing sugar was quantitatively determined by the 3,5-dinitrosalicylic acid (DNS) method (Miller, G. L., et al., Anal. Biochem., 2, 127 (1960)). The amount of enzyme which produces a quantity per minute of reducing sugar equivalent to 1 μmol of glucose is taken as 1 unit. As a result, pullulanase activity was detected in a cell-free extract of strain HB101(pPU100). Further, when the optimum working pH of the produced pullulanase was measured, it was found that the pullulanase was in fact an alkaline pullulanase having the optimum working pH of pH 9.5. For the measurement of enzymatic activity, the following buffers (each at 40 mM) were used:

pH 3.5-5.5: Acetate buffer

pH 5.5-8.5: Tris-maleic acid buffer

pH 8.5-10.5: Glycine-NaCl—NaOH buffer

pH 10.5-11.0: Na 2 CO 3 —NaHCO 3 buffer

Example 5

Southern Hybridization of Alkaline Amylopullulanase Gene With PstI Digested Chromosomal DNAs of Bacillus sp. KSM-AP1378

About 5 μg of pPU100 was cleaved with a restriction enzyme PstI and was then subjected to electrophoresis on an agarose gel. From the gel, about 0.5 μg of a PstI fragment having a size of about 6.3 kb was isolated using a Geneclean kit (Biolol Inc.). The PstI fragment was labelled using a DNA labelling & detection kit (Boehringer Mannheim) to prepare a probe DNA. Independently, chromosomal DNAs (3 μg each) derived from Bacillus sp. KSM-AP1378 cleaved with PstI were subjected to electrophoresis on an agarose gel, and the DNA bands were transferred onto a nylon membrane (Amersham) using a method proposed by Southern (Southern, E. M., J. Mol. Biol., 98, 503 (1975)). Hybridization with the probe DNA was investigated using a DNA labelling & detection kit. As a result, in PstI cleavage products of chromosomal DNAs derived from the KSM-AP1378 strain, presence of a DNA fragment having a size of about 6.3 kb that hybridized with the probe DNA was detected as shown in FIG. 4 . Thus, the PstI fragment having a size of about 6.3 kb contained in plasmid pPU100 was confirmed to be originated from the chromosomal DNA of Bacillus sp. KSM-AP1378.

Example 6

Construction of Plasmid Containing DNA Fragment Encoding Alkaline Pullulanase

A recombinant plasmid pHYPUL was created by inserting, between the PstI site and the BamHI site of plasmid pHY300PLK, a fragment having a size of about 3.5 kb (fragment B, FIG. 1 ) and obtained by cleaving a PstI fragment having a size of about 6.3 kb contained in plasmid pPU100 with BamHI. E. coli HB101 was transformed with the thus-created recombinant plasmid, and pullulanase activity was measured through a method similar to that of Example 4. As a result, a pullulanase activity having an optimum working pH in the pH range from 9 to 10 was observed. Thus, the essential domain of alkaline pullulanase was elucidated to be a stretch of about 3.5 kb from the PstI site to the BamHI site.

Example 7

Sequencing of DNA Fragments Encoding Alkaline Pullulanase

Using the fragment B obtained in Example 6, a commercially available deletion kit (Kilosequence Deletion kit, Takara Shuzo), and two suitable restriction enzymes, recombinant plasmid DNAs containing resultant reduced fragments were created, and the nucleotide sequences of the inserted fragments were determined. Nucleotide sequence was determined using a DNA sequencer (Model 370A, Applied Biosystems) and Taq-Dydeoxy Cycle Sequencing kit (Applied Biosystems) in accordance with a method using a fluorescent primer (Smith, L. M., et al., Nature, 321, 674 (1986)). By overlapping nucleotide sequences having sizes of about 300-450 bp from respective DNA samples, the 3038 bp sequence on the PstI site side of fragment B was determined. As a result, the open reading frame (ORF) of the alkaline pullulanase gene was found to continue to the upstream side of the PstI site, which is a terminus of the obtained fragment having a size of about 6.3 kb. Restriction Mapping of the Alkaline Amylopullulanase Gene

Example 8

Using a fragment of about 6.3 kb as shown in FIG. 1 , a PstI-XbaI 1.5 kb fragment (fragment C) was created, and labelled in a manner similar to that described in Example 5 to prepare a probe DNA (probe 1 ). Separately, chromosomal DNAs derived from Bacillus sp. KSM-AP1378 which had been cleaved with XbaI (3 μg each) were subjected to electrophoresis on an agarose gel, and the resultant DNA bands were transferred onto a nylon membrane (Amersham) in a manner similar to that described in Example 5, followed by hybridization with the probe. As a result, probe 1 was found to hybridize with an XbaI fragment having a size of about 2.3 kb, and from this, it was deduced that there exists an XbaI site about 0.8 kb upstream of a 6.3 kb fragment PstI-PstI on the chromosomal DNA derived from the KSM-AP1378 strain (FIG. 1 ). The stretch from the PstI site to the XbaI site having a length of about 0.8 kb was amplified using primers 1 and 2 ( FIGS. 1 and 6 ) each having 24 nucleotides and synthesized based on the nucleotide sequence determined in Example 7, circular DNAs (which were obtained through intramolecular ligation of chromosomal DNA of KSM-AP1378 cleaved with XbaI) which served as templates, and a PCR kit (Applied Biosystems) in accordance with an inverse PCR method (Triglia, T. et al., Nucleic Acids Res., 16, 81 (1988); one cycle=94° C.×1 min.+55° C.×1 min.+72° C.×3 min., 30 cycles). The sequence of the 0.8 kb fragment (fragment D) which had undergone the above amplification was determined in a manner similar to that described in Example 7. As a result, it was found that the ORF of alkaline pullulanase which continued from fragment C further extended to the upstream of fragment D (FIG. 1 ).

Example 9

The fragment having a size of about 0.8 kb and stretching from XbaI to PstI obtained in Example 8 was labelled in a manner similar to that described in Example 5 to prepare a probe DNA (probe 2). Separately, chromosomal DNAs derived from Bacillus sp. KSM-AP1378 which had been cleaved with EcoRI (3 μg each) were subjected to electrophoresis on an agarose gel, and the resultant DNA bands were transferred onto a nylon membrane (Amersham) in a manner similar to that described in Example 5, followed by hybridization with probe 2 . From the size of a hybridized EcoRI fragment (3.6 kb, FIG. 7 ), it was deduced that there exists an EcoRI site 1.2 kb upstream of fragment D obtained in Example 8. The stretch from the XbaI site to 1.2 kb upstream of this site was amplified using primers 3 and 4 ( FIGS. 1 and 6 ) having 24 nucleotides and synthesized based on the nucleotide sequence determined in Example 8 and circular DNAs (which were obtained through intramolecular ligation of chromosomal DNA of strain KSM-AP1378 cleaved with EcoRI) which served as templates in accordance with an inverse PCR method in a manner similar to that described in Example 8 (fragment E). The sequence of the 1.2 kb fragment which had undergone the above amplification was determined in a manner similar to that described in Example 7. As a result, it was found that the ORF of alkaline pullulanase which continued from fragment D further extended to the upstream of fragment E.

Example 10

The fragment E obtained in Example 9 was labelled in a manner similar to that described in Example 5 to prepare a probe DNA (probe 3 ). In a manner similar to Examples 8 and 9, hybridization analysis was performed on XbaI cleavage products of the chromosomal DNA derived from strain KSM-AP1378 (FIG. 8 ). As a result, as shown in FIG. 1 , it was deduced that there exists an XbaI site 1.1 kb upstream of the EcoRI site of fragment D in the chromosomal DNA derived from strain KSM-AP1378. The stretch from the EcoRI site to 1.1 kb upstream of this site was amplified using primers 5 and 6 ( FIGS. 1 and 6 each having 24 nucleotides and synthesized based on the nucleotide sequence determined in Example 9 and circular DNAs (which were obtained through intramolecular ligation of chromosomal DNA of strain KSM-AP1378 cleaved with XbaI) which served as templates in accordance with an inverse PCR method in a manner similar to that described in Example 8. The sequence of the 1.1 kb fragment (fragment F) which had undergone the above amplification was determined in a manner similar to that described in Example 7. As a result, it was confirmed that the 5′ region of the ORF of alkaline pullulanase gene which continued from fragment E existed in this fragment. The complete nucleotide sequence of the present gene and a deduced amino acid sequence are described in SEQ ID NO:1. Based on the fact that the putative sequence of Nos. 1 through 14 amino acids coincided with the sequence of amino terminus actually determined on Bacillus sp. KSM-AP1378 using alkaline amylopullulanase, it was presumed that the present gene encoded alkaline amylopullulanase.

Example 11

A 3.5 kb fragment (fragment G) containing an alkaline α-amylase domain of the alkaline amylopullulanase gene was amplified using primers A and B ( FIGS. 1 and 6 ) each having 25 nucleotides and synthesized based on the nucleotide sequence determined in Examples 7 and 10, the chromosomal DNA of strain KSM-AP1378 as a template, and a PCR kit (Applied Biosystems) in accordance with a PCR method (one cycle=94° C.×1 min.+55° C.×1 min.+72° C.×3 min., 30 cycles). The resultant DNA fragment was inserted into the SmaI site of a pUC18 plasmid vector, and then subjected to transformation using commercially available E. coli HB101 competent cells. The obtained transformants were replicated onto an LB medium containing 0.4% blue starch (Starch azure, Sigma) and 50 μg/ml of ampicillin, followed by culturing at 37° C. for 12 hours. A single strain which decomposed blue starch and thus formed a halo around its colony was isolated. In a manner similar to that described in Example 3, a plasmid (pAMY100) was prepared from this strain.

Example 12

Recombinant Production of Alkaline Amylopullulanase

A recombinant plasmid mixture was prepared by ligating, using a T4 ligase, a 7.7 kb fragment obtained by cleaving a plasmid pHYPUL (Example 3) containing an alkaline pullulanase domain of the alkaline amylopullulanase and pAMY100 (Example 11) containing the alkaline α-amylase domain of the same gene. E. coli HB101 was transformed with the recombinant plasmid mixture, and each of transformants which emerged was replicated onto an LB medium containing 0.4% blue starch and 50 μg/ml of ampicillin and also onto another LB medium containing 0.8% red pullulan (Kanno, M. and Tomiura, E., Agric. Biol. Chem., 49, 1529 (1985)) and 50 μg/ml of ampicillin, followed by culturing for growth at 37° C. for 12 hours. A strain which formed a halo around its colony on both plates was isolated as a recombinant E. coli capable of producing the alkaline amylopullulanase.

Example 13

Using the recombinant E. coli obtained in Example 12, about 500 μg of a recombinant plasmid was prepared in a manner similar to that described in Example 3. From a restriction enzyme map of the resultant recombinant plasmid, it was found that the plasmid contained a DNA fragment (fragment H) of about 7.0 kb as shown in FIG. 1 . This plasmid was named pAP101 (FIG. 2 ). E. coli HB101 transformed with the plasmid pAP101 was named HB101(pAP101).

Example 14

A cell-free extract was prepared using E. coli HB101(pAP101) in a manner similar to that described in Example 4. A control cell-free extract was also prepared using the HB101(pBR322) strain. α-Amylase and pullulanase activities of these extracts were measured. The α-amylase activity was measured by causing a reaction, at 50° C. for 15 minutes, in a reaction mixture containing 50 mM glycine-NaCl—NaOH buffer (pH 10) and soluble starch, and the resultant reducing sugar was quantitatively determined by the DNS method. The pullulanase activity was measured in a manner similar to that described in Example 4. In both cases, the amount of enzyme which produced a quantity per minute of reducing sugar equivalent to 1 μmol of glucose was taken as 1 unit. As a result, α-amylase and pullulanase activities were detected in a cell-free extract of strain HB101(pAP101). When the optimum working pHs of α-amylase and pullulanase were measured as described in Example 4, it was found that the maximum α-amylase activity and the maximum pullulanase activity were observed in pH ranges from 8 to 9 and from 9 to 10, respectively.

Example 15

Characterization of Alkaline Amylopullulanase

To 50 mg of an alkaline amylopullulanase enzyme (210 kDa; Japanese Patent Publication (kokoku) No. 6-32613) purified from a culture of Bacillus sp. KSM-AP1378, 0.1 mg of papain (Sigma, 5 U/mg) was added and hydrolysis was allowed to proceed at 30° C. for 2 minutes. Subsequently, the reaction was stopped by the addition of 10 μg of antipain (Furuka). The resulting decomposition product was fractionated using a DEAE 5PW column (7.5 mm×7.5 cm; Tosoh) to obtain protein fragments with 114 kDa and 102 kDa. Measurement of enzymatic activities of these two protein fragments revealed that the 102 kDa protein fragment possessed only alkaline pullulanase activity and the 114 kDa protein fragment possessed only alkaline α-amylase activity. The N-terminus of the amino acid sequence of the 102 kDa protein fragment possessing only pullulanase activity was determined to have the sequence Thr-Val-Pro-Leu-Ala-Leu-Val-Ser-Gly-Glu-Val-Leu-Ser-Asp-Lys-Leu, which agreed perfectly with 1014th-1029th amino acids deduced from the amino acid sequence described in SEQ ID NO: 2. Similarly, the N-terminus of the amino acid sequence of the 114 kDa protein fragment possessing only α-amylase activity was determined to have the sequence Glu-Thr-Gly-Asp-Lys-Arg-Ile-Glu-Phe-Ser-Tyr-Glu-Arg-Pro, which agreed perfectly with 1st-14th amino acids deduced from the amino acid sequence described in SEQ ID NO: 2. These results also proved that the present gene encodes an alkaline amylopullulanase protein having different active centers, i.e., active centers for pullulanase activity and for α-amylase activity.

Example 16

The recombinant plasmid pAP101 was introduced in B. subtilis ISW1214 and the transformed cells were grown at 31° C. for 60 hours, with shaking, in LB medium containing 15 μg/ml of tetraglycine. The alkaline amylopullulanase was found to be excreted at a level of 60 units per liter, in terms of the alkaline pullulanase activity. The expressed enzymes had pH optima of around 8-9 for the amylase activity and at 9.5 for the pullulanase activity, values close to the pH optima for the respective enzymatic activities of the alkaline amylopullulanase of Bacillus sp. KSM-AP1378. The molecular mass of the expressed amylopullulanase protein was approximately 200-210 kDa by sodium dodecyl sulfate gel electrophoresis, a value close to the enzyme of strain KSM-AP1378.

Reference Example 1

A Bacillus sp. KSM-AP1378 strain which produces alkaline amylopullulanase was inoculated into 10 ml of medium A (Table 1) and subjected to shaking culture at 30° C. for 2 days. Ten (10) ml of the culture was inoculated in 1 liter of the same medium, followed by shaking culture at 30° C. for a further 3 days. Subsequently, cells were centrifugally processed to obtain a crude enzymatic liquid containing alkaline amylopullulanase. This crude enzymatic liquid was purified through various treatments including adsorption onto DEAE cellulose, affinity chromatography on a column of Sepharose-α-cyclodextrin, and gel filtration on a column of Sephacryl S-200 to obtain an electrophoretically homogeneous sample of the enzyme. Using a protein sequencer 476A (Applied Biosystems), the N-terminus of the amino acid sequence of this enzyme was determined to have the sequence Glu-Thr-Gly-Asp-Lys-Arg-Ile-Glu-Phe-Ser-Tyr-Glu-Arg-Pro.

Reference Example 2

The optimum pHs for the α-amylase activity and pullulanase activity of alkaline amylopullulanase obtained in Reference example 1 were determined using a method described in Examples 4 and 14. As a result, the optimum pH for α-amylase activity was observed in the vicinity of pH 8.5, and that for pullulanase activity was observed in the vicinity of pH 9.5.

INDUSTRIAL APPLICABILITY

According to the present invention, it is possible to obtain a gene coding for alkaline amylopullulanase exhibiting the maximum activity in an alkaline pH range as well as a microorganism harboring such gene. Use of the present invention facilitates mass production of alkaline amylopullulanase. Alkaline amylopullulanase is characteristic in that it has different active centers, one for α-amylase and one for pullulanase, in a single protein of the enzyme.

14 1 6142 DNA Bacillus sp. CDS (145)..(5958) sig_peptide (145)..(240) mat_peptide (241)..(5958) 1tctagatgtg caattttgcg caaacgattt cacatttaca taaacaatct tggcatcaat 60taaattattt attgtgcaac tttgtgcaaa cgcttccaca ttttagcaag aaatgcaaat 120cattgtatgg aaaggggcag ggat atg aag aaa agg ttt caa agg ggt atg 171 Met Lys Lys Arg Phe Gln Arg Gly Met -30 -25gct ggt tta ctt tct att tta ctt att gtt tcc atg ttt gca ggc tat 219Ala Gly Leu Leu Ser Ile Leu Leu Ile Val Ser Met Phe Ala Gly Tyr -20 -15 -10cta ccg gca aga gca gcg gcc gaa acg gga gac aag cgg ata gaa ttc 267Leu Pro Ala Arg Ala Ala Ala Glu Thr Gly Asp Lys Arg Ile Glu Phe -5 -1 1 5agt tat gaa cgg cca gat gga aat tat gaa ggc tgg aat tta tgg gtc 315Ser Tyr Glu Arg Pro Asp Gly Asn Tyr Glu Gly Trp Asn Leu Trp Val 10 15 20 25tgg gga act ggt gtg aag gat gac cag ata gac ttt aca gaa ttc aag 363Trp Gly Thr Gly Val Lys Asp Asp Gln Ile Asp Phe Thr Glu Phe Lys 30 35 40gaa ggc aag gca tat gcc gac ata gca gta agc gat aat gcg gat aaa 411Glu Gly Lys Ala Tyr Ala Asp Ile Ala Val Ser Asp Asn Ala Asp Lys 45 50 55gtc ggt ttc att atc cgt aaa ggg gat tgg gaa gaa aag gac ttt gat 459Val Gly Phe Ile Ile Arg Lys Gly Asp Trp Glu Glu Lys Asp Phe Asp 60 65 70ggg gac agg tcg att acg atc aat aag atc gat aac atc acc aaa gtg 507Gly Asp Arg Ser Ile Thr Ile Asn Lys Ile Asp Asn Ile Thr Lys Val 75 80 85cat gta aca agc cag cag gaa aaa ttc ggg caa att cct gac ggc agc 555His Val Thr Ser Gln Gln Glu Lys Phe Gly Gln Ile Pro Asp Gly Ser 90 95 100 105cca cct gtt gtt gcg gac ggg aat gct gac ttc ttt ttc cgt gat aaa 603Pro Pro Val Val Ala Asp Gly Asn Ala Asp Phe Phe Phe Arg Asp Lys 110 115 120gaa ctg tac gca gca gga gaa atg gat aag gtt gag aaa gtc gaa ctg 651Glu Leu Tyr Ala Ala Gly Glu Met Asp Lys Val Glu Lys Val Glu Leu 125 130 135tcc att tta ggc gaa aaa tac gag atg aat ggt gag ccg gaa aag gag 699Ser Ile Leu Gly Glu Lys Tyr Glu Met Asn Gly Glu Pro Glu Lys Glu 140 145 150cgt ttt aca tat aca tta agc gat ctt cct aca ggc gag cat gaa tat 747Arg Phe Thr Tyr Thr Leu Ser Asp Leu Pro Thr Gly Glu His Glu Tyr 155 160 165act tat ttg gtg aca gtg gat gga cag aca gag gaa gtt acc gat cca 795Thr Tyr Leu Val Thr Val Asp Gly Gln Thr Glu Glu Val Thr Asp Pro170 175 180 185tat aac acg gtg gat gga agg tct gtt gtg gag tat gtg aca tcc gat 843Tyr Asn Thr Val Asp Gly Arg Ser Val Val Glu Tyr Val Thr Ser Asp 190 195 200gtg caa gta tcg gct tca ttt ata ccc gca aag gtt gat tat aac cag 891Val Gln Val Ser Ala Ser Phe Ile Pro Ala Lys Val Asp Tyr Asn Gln 205 210 215aac gct gtg gtg aag gta gac atc gaa tca gaa acg gag aca aaa atc 939Asn Ala Val Val Lys Val Asp Ile Glu Ser Glu Thr Glu Thr Lys Ile 220 225 230cgt gag atg tct atc aat ctt tca gaa atc ggc ggc aaa gag aaa gca 987Arg Glu Met Ser Ile Asn Leu Ser Glu Ile Gly Gly Lys Glu Lys Ala 235 240 245acc att gat cct gcg ctg aat gaa ttg aca gtt gcg gtc aag caa ggt 1035Thr Ile Asp Pro Ala Leu Asn Glu Leu Thr Val Ala Val Lys Gln Gly250 255 260 265gtg acg gca ggt gtg aaa aac ttg cct atc act gcg att gat gaa ttc 1083Val Thr Ala Gly Val Lys Asn Leu Pro Ile Thr Ala Ile Asp Glu Phe 270 275 280gga aat cgc cat gag gga tct gct acc tta gaa gtt cag gcg cgt act 1131Gly Asn Arg His Glu Gly Ser Ala Thr Leu Glu Val Gln Ala Arg Thr 285 290 295att aca ggt gaa aaa gca gat ttc gac tgg gat cag tct gtg gtt tat 1179Ile Thr Gly Glu Lys Ala Asp Phe Asp Trp Asp Gln Ser Val Val Tyr 300 305 310ttt atg ctg aca gat cga ttc ttt gat ggg gat tca tcg aac aat gac 1227Phe Met Leu Thr Asp Arg Phe Phe Asp Gly Asp Ser Ser Asn Asn Asp 315 320 325cct cat ggt att ggc tat gac aca agc aag tct ggt aca tac caa ggc 1275Pro His Gly Ile Gly Tyr Asp Thr Ser Lys Ser Gly Thr Tyr Gln Gly330 335 340 345gga gat ttt aag ggg atc acg caa agg ctt gat tac ttg gac gag ctt 1323Gly Asp Phe Lys Gly Ile Thr Gln Arg Leu Asp Tyr Leu Asp Glu Leu 350 355 360gga atc aat acg atc tgg atc agt ccg gtt gtc gat aat atc aaa ttt 1371Gly Ile Asn Thr Ile Trp Ile Ser Pro Val Val Asp Asn Ile Lys Phe 365 370 375gat gtt cga cac agt gaa gga cct gat aca cca tat tat gct tac cac 1419Asp Val Arg His Ser Glu Gly Pro Asp Thr Pro Tyr Tyr Ala Tyr His 380 385 390ggc tat tgg gcg gat aat ttc ggg gaa ttg aac ccg cat ttc ggt tcc 1467Gly Tyr Trp Ala Asp Asn Phe Gly Glu Leu Asn Pro His Phe Gly Ser 395 400 405atg gcg gat ttc cat gaa atg att gat gcg gca cat gaa cgc ggc att 1515Met Ala Asp Phe His Glu Met Ile Asp Ala Ala His Glu Arg Gly Ile410 415 420 425aaa atc atg gtt gat gtg gtg ttg aat cac act ggt tat gga ttg aaa 1563Lys Ile Met Val Asp Val Val Leu Asn His Thr Gly Tyr Gly Leu Lys 430 435 440cca ggt gac agc agc agt gtg gcg aac ttc ccg aca gat gag gac cga 1611Pro Gly Asp Ser Ser Ser Val Ala Asn Phe Pro Thr Asp Glu Asp Arg 445 450 455gct cgc ttt gac gga atg ctt cgt gat ggc gga tct ggt gaa gtt cga 1659Ala Arg Phe Asp Gly Met Leu Arg Asp Gly Gly Ser Gly Glu Val Arg 460 465 470ggc gag ctt gct ggc ctt cca gat ttt ctg acg gaa aac ccg gat gtc 1707Gly Glu Leu Ala Gly Leu Pro Asp Phe Leu Thr Glu Asn Pro Asp Val 475 480 485cgt gaa cag gtg gtg caa tgg cag acg gac tgg atc gaa aag tcc agg 1755Arg Glu Gln Val Val Gln Trp Gln Thr Asp Trp Ile Glu Lys Ser Arg490 495 500 505acg gca aag ggc aac acc atc gat tat ttc cgt gtc gac acc gtc aag 1803Thr Ala Lys Gly Asn Thr Ile Asp Tyr Phe Arg Val Asp Thr Val Lys 510 515 520cat gtg gaa gac acc act tgg atg gcg ttt aaa aat gct ttg aca aaa 1851His Val Glu Asp Thr Thr Trp Met Ala Phe Lys Asn Ala Leu Thr Lys 525 530 535gcg atg ccg gaa cac aag ctg att ggg gaa gca tgg gga gca aat gtc 1899Ala Met Pro Glu His Lys Leu Ile Gly Glu Ala Trp Gly Ala Asn Val 540 545 550aat gac gac cta ggt tat ctg aac agc gga atg atg gat tct tta ctg 1947Asn Asp Asp Leu Gly Tyr Leu Asn Ser Gly Met Met Asp Ser Leu Leu 555 560 565gat ttt gat ttc aaa aat tat gcc cgt gac ttt gca aac gga cag ctg 1995Asp Phe Asp Phe Lys Asn Tyr Ala Arg Asp Phe Ala Asn Gly Gln Leu570 575 580 585gat gcg gtt cag caa aaa ctt gag gcg cgt aac agc aag ttg aac aat 2043Asp Ala Val Gln Gln Lys Leu Glu Ala Arg Asn Ser Lys Leu Asn Asn 590 595 600act gca aca ctt ggt caa ttt tta gga agc cat gac gaa gac cgc ttc 2091Thr Ala Thr Leu Gly Gln Phe Leu Gly Ser His Asp Glu Asp Arg Phe 605 610 615tat gag gtg gtg gaa gga gac ctt ggc aag tat caa gtt gct gca tcc 2139Tyr Glu Val Val Glu Gly Asp Leu Gly Lys Tyr Gln Val Ala Ala Ser 620 625 630ctt caa ctg acg gca aag ggt cag cct gtt atc tat tac gga gaa gag 2187Leu Gln Leu Thr Ala Lys Gly Gln Pro Val Ile Tyr Tyr Gly Glu Glu 635 640 645ctg ggc ttg cct ggt aag aac gat tat ccg tat tat acg aac cgc cag 2235Leu Gly Leu Pro Gly Lys Asn Asp Tyr Pro Tyr Tyr Thr Asn Arg Gln650 655 660 665aac atg cct tgg gat gat gtg gat ggt aat gaa att cta gag cat tat 2283Asn Met Pro Trp Asp Asp Val Asp Gly Asn Glu Ile Leu Glu His Tyr 670 675 680caa aaa tta ctg gca ttc cgt aat gat aat ccg aac aca ttt gct aaa 2331Gln Lys Leu Leu Ala Phe Arg Asn Asp Asn Pro Asn Thr Phe Ala Lys 685 690 695gga gac cgc aaa aag gta gcg gga tct gac agt gaa gga tat ctt tta 2379Gly Asp Arg Lys Lys Val Ala Gly Ser Asp Ser Glu Gly Tyr Leu Leu 700 705 710ttt tca cgg acg tac ggg gaa aat tcc gtt tat gta ggt ttg aat acg 2427Phe Ser Arg Thr Tyr Gly Glu Asn Ser Val Tyr Val Gly Leu Asn Thr 715 720 725gaa gct gct gcg aaa gac gta acc ttg aac ttc ggt tct tca gaa gca 2475Glu Ala Ala Ala Lys Asp Val Thr Leu Asn Phe Gly Ser Ser Glu Ala730 735 740 745gtg gtg acg gac cgc tat tcc ggt cag gag tac caa gca aat gaa gaa 2523Val Val Thr Asp Arg Tyr Ser Gly Gln Glu Tyr Gln Ala Asn Glu Glu 750 755 760ggc caa gtg acg ttc tct att ccg gcg atg gaa gac ggg gga acg gtc 2571Gly Gln Val Thr Phe Ser Ile Pro Ala Met Glu Asp Gly Gly Thr Val 765 770 775ctg ctt gaa gtg gaa aat gga gca gtg cca cct gtg gag gaa gaa cca 2619Leu Leu Glu Val Glu Asn Gly Ala Val Pro Pro Val Glu Glu Glu Pro 780 785 790act gag cca ggt gaa atc gaa gaa aac acg ctt cgg att cac tac cag 2667Thr Glu Pro Gly Glu Ile Glu Glu Asn Thr Leu Arg Ile His Tyr Gln 795 800 805cgc aca gac aac agc tac gaa aac ctt ggt cta tgg tta tgg gga gac 2715Arg Thr Asp Asn Ser Tyr Glu Asn Leu Gly Leu Trp Leu Trp Gly Asp810 815 820 825gtc gcg gca cca tct gaa aac tgg cca tca ggc ggc aca ccg ttc caa 2763Val Ala Ala Pro Ser Glu Asn Trp Pro Ser Gly Gly Thr Pro Phe Gln 830 835 840gca ggt aat gta aca gac tat ggt gca tat gtc gat gtg gaa ttg gca 2811Ala Gly Asn Val Thr Asp Tyr Gly Ala Tyr Val Asp Val Glu Leu Ala 845 850 855gaa gat gct caa aat att gga ttc ctt gtt ttg aac acc aca aac ggt 2859Glu Asp Ala Gln Asn Ile Gly Phe Leu Val Leu Asn Thr Thr Asn Gly 860 865 870gac aag gac ggc ggc gac aaa gca gta gaa ttg ttc agt ccg gat tta 2907Asp Lys Asp Gly Gly Asp Lys Ala Val Glu Leu Phe Ser Pro Asp Leu 875 880 885aat gag att tgg atc aaa caa ggc tct gat gaa gta ttt tta tat gaa 2955Asn Glu Ile Trp Ile Lys Gln Gly Ser Asp Glu Val Phe Leu Tyr Glu890 895 900 905ccg gtg gac ctt ccg gca aat acg gtc cgc att cat tat gaa aga acc 3003Pro Val Asp Leu Pro Ala Asn Thr Val Arg Ile His Tyr Glu Arg Thr 910 915 920aat gcc gac tat gaa ggc tgg ggg tta tgg aac tgg gag gat gtc gag 3051Asn Ala Asp Tyr Glu Gly Trp Gly Leu Trp Asn Trp Glu Asp Val Glu 925 930 935tcc cca tct gac ggg tgg ccg aac ggt gcc gca gat gct gca ggt atc 3099Ser Pro Ser Asp Gly Trp Pro Asn Gly Ala Ala Asp Ala Ala Gly Ile 940 945 950ggt aaa tac ggt gct tac tac gac atc aag ctg aaa gaa gat gct aat 3147Gly Lys Tyr Gly Ala Tyr Tyr Asp Ile Lys Leu Lys Glu Asp Ala Asn 955 960 965aaa att ggt ttc ctt ttt gtg aac aaa caa tct ggt ggc caa acg gga 3195Lys Ile Gly Phe Leu Phe Val Asn Lys Gln Ser Gly Gly Gln Thr Gly970 975 980 985gat atg acg ttt gat atg ctg aaa caa tac aac caa ctt ttt gta aaa 3243Asp Met Thr Phe Asp Met Leu Lys Gln Tyr Asn Gln Leu Phe Val Lys 990 995 1000gag ggc gag gac aag gtc tac acc aat cct tac ggg acc gtg cca ttg 3291Glu Gly Glu Asp Lys Val Tyr Thr Asn Pro Tyr Gly Thr Val Pro Leu 1005 1010 1015gcg ctt gtg tct gga gag gta ttg tca gac aag ttg atc agt ctt act 3339Ala Leu Val Ser Gly Glu Val Leu Ser Asp Lys Leu Ile Ser Leu Thr 1020 1025 1030ttt acc agg aca gaa gga ttg gat ttg gag gaa ttg aaa gaa cag cta 3387Phe Thr Arg Thr Glu Gly Leu Asp Leu Glu Glu Leu Lys Glu Gln Leu 1035 1040 1045gaa atc aag gat gtg gac ggg aac gat gtt tcg ttt aca gat gtg aca 3435Glu Ile Lys Asp Val Asp Gly Asn Asp Val Ser Phe Thr Asp Val Thr1050 1055 1060 1065att gaa ggc gag aaa acg gtc cat gtc cac ggc gag ttt gac ttg gag 3483Ile Glu Gly Glu Lys Thr Val His Val His Gly Glu Phe Asp Leu Glu 1070 1075 1080aaa atc ccg ttc tct gtg acc tat ctg gac cgc acc att tct gta aaa 3531Lys Ile Pro Phe Ser Val Thr Tyr Leu Asp Arg Thr Ile Ser Val Lys 1085 1090 1095tca ggc tgg aaa ctg atc gac gaa atg tat gcc tat gat gga aag ctt 3579Ser Gly Trp Lys Leu Ile Asp Glu Met Tyr Ala Tyr Asp Gly Lys Leu 1100 1105 1110ggg gca gaa ttg cat gaa gac ggg acg gct act ttg aaa gta tgg tcg 3627Gly Ala Glu Leu His Glu Asp Gly Thr Ala Thr Leu Lys Val Trp Ser 1115 1120 1125cca aaa gcg gac aat gtg tct gtt gta ctt tat gac aaa gtt gac cag 3675Pro Lys Ala Asp Asn Val Ser Val Val Leu Tyr Asp Lys Val Asp Gln1130 1135 1140 1145aac gag gtt gta gac acc att gaa atg gta aaa ggg gac cgc ggt gtc 3723Asn Glu Val Val Asp Thr Ile Glu Met Val Lys Gly Asp Arg Gly Val 1150 1155 1160tgg tct gta aag cta act aag gat aat aca ggc ctt gat agt ttg aaa 3771Trp Ser Val Lys Leu Thr Lys Asp Asn Thr Gly Leu Asp Ser Leu Lys 1165 1170 1175ggt tac tat tac cac tat gaa atc acg cat ggt gac gta acg aat ctt 3819Gly Tyr Tyr Tyr His Tyr Glu Ile Thr His Gly Asp Val Thr Asn Leu 1180 1185 1190gct cta gat ccg tat gcc aaa tca atg gcg gcg tgg aat aac gaa gcg 3867Ala Leu Asp Pro Tyr Ala Lys Ser Met Ala Ala Trp Asn Asn Glu Ala 1195 1200 1205ggg gac aag gta gga aaa gcg gcg atc gtg gac atc ggc tcc att ggg 3915Gly Asp Lys Val Gly Lys Ala Ala Ile Val Asp Ile Gly Ser Ile Gly1210 1215 1220 1225cct gag ctt gat tat gcc gac atc cct ggc ttt gaa aag cgc gaa gac 3963Pro Glu Leu Asp Tyr Ala Asp Ile Pro Gly Phe Glu Lys Arg Glu Asp 1230 1235 1240acc atc atc tac gag gtg cat gta cgt gac ttc act tcc gac ccg aat 4011Thr Ile Ile Tyr Glu Val His Val Arg Asp Phe Thr Ser Asp Pro Asn 1245 1250 1255atc ggt gag gac ctg aag gca cag ttc ggt aca ttt gct tct ttc gtg 4059Ile Gly Glu Asp Leu Lys Ala Gln Phe Gly Thr Phe Ala Ser Phe Val 1260 1265 1270gaa aag ctg gat tac att caa gag tta ggt gtc act cac att caa ttg 4107Glu Lys Leu Asp Tyr Ile Gln Glu Leu Gly Val Thr His Ile Gln Leu 1275 1280 1285ttg cct gtg atg agc tat tat ttc agc aat gaa ttt gag tct ggg gag 4155Leu Pro Val Met Ser Tyr Tyr Phe Ser Asn Glu Phe Glu Ser Gly Glu1290 1295 1300 1305cgc atg ctg gag tat gct tca acg ggg acg aat tac aat tgg ggc tat 4203Arg Met Leu Glu Tyr Ala Ser Thr Gly Thr Asn Tyr Asn Trp Gly Tyr 1310 1315 1320gac ccg cac aat tac ttc tcc tta tcc ggc atg tac tcc gaa aac cct 4251Asp Pro His Asn Tyr Phe Ser Leu Ser Gly Met Tyr Ser Glu Asn Pro 1325 1330 1335gag gac ccg gaa ctg aga atc aaa gaa ttc aag aat ctg atc aac gag 4299Glu Asp Pro Glu Leu Arg Ile Lys Glu Phe Lys Asn Leu Ile Asn Glu 1340 1345 1350att cat aag cgc gac atg ggt gtg gta ctt gat gtg gtg ttt aac cac 4347Ile His Lys Arg Asp Met Gly Val Val Leu Asp Val Val Phe Asn His 1355 1360 1365acc gca cag gtt cac att ttc gag gac ctt gta cca aac tac tat cac 4395Thr Ala Gln Val His Ile Phe Glu Asp Leu Val Pro Asn Tyr Tyr His1370 1375 1380 1385ttc atg gat gcg gac gga acc cca aga act agc ttt ggc ggt gga cgt 4443Phe Met Asp Ala Asp Gly Thr Pro Arg Thr Ser Phe Gly Gly Gly Arg 1390 1395 1400ctt gga acg aca cat gaa atg tcc cgc cgt gtg ctc gta gat tcc atc 4491Leu Gly Thr Thr His Glu Met Ser Arg Arg Val Leu Val Asp Ser Ile 1405 1410 1415aag cat tgg gtg gat gaa tat aag gtg gac gga ttc cgt ttt gac atg 4539Lys His Trp Val Asp Glu Tyr Lys Val Asp Gly Phe Arg Phe Asp Met 1420 1425 1430atg ggt gac cat gat gca gag agt att cag att gct ttt gac gaa gcc 4587Met Gly Asp His Asp Ala Glu Ser Ile Gln Ile Ala Phe Asp Glu Ala 1435 1440 1445aaa aaa ttg aac ccg aat atc gtc atg atc ggg gaa ggc tgg gta aca 4635Lys Lys Leu Asn Pro Asn Ile Val Met Ile Gly Glu Gly Trp Val Thr1450 1455 1460 1465ttt gct ggt gac gag ggc gag ccg gtc cag gcg gcc gat caa caa tgg 4683Phe Ala Gly Asp Glu Gly Glu Pro Val Gln Ala Ala Asp Gln Gln Trp 1470 1475 1480atg caa tat acc gaa gca gtg ggt agc ttc tcg gat gaa ttc cgc aac 4731Met Gln Tyr Thr Glu Ala Val Gly Ser Phe Ser Asp Glu Phe Arg Asn 1485 1490 1495gag ctg aaa tcc ggt ttc gga agc gaa gga cag cca cgt ttc atc aca 4779Glu Leu Lys Ser Gly Phe Gly Ser Glu Gly Gln Pro Arg Phe Ile Thr 1500 1505 1510ggt ggc gcg gtc aat gtg caa caa att ttc gat aac atc aaa gca cag 4827Gly Gly Ala Val Asn Val Gln Gln Ile Phe Asp Asn Ile Lys Ala Gln 1515 1520 1525cct cat aac ttt atg gcc gat caa cca ggc gat gtg gtc caa tac atc 4875Pro His Asn Phe Met Ala Asp Gln Pro Gly Asp Val Val Gln Tyr Ile1530 1535 1540 1545gag gcc cat gac aac ctg acg tta tac gat gtc atc gca caa tct atc 4923Glu Ala His Asp Asn Leu Thr Leu Tyr Asp Val Ile Ala Gln Ser Ile 1550 1555 1560aaa aaa gat ccg gaa atc gcg gaa aac gat tta gag att cat aag cgt 4971Lys Lys Asp Pro Glu Ile Ala Glu Asn Asp Leu Glu Ile His Lys Arg 1565 1570 1575att cgc gtg ggt aat gcc atg gtc ttg acg tct caa ggt acg gca ttc 5019Ile Arg Val Gly Asn Ala Met Val Leu Thr Ser Gln Gly Thr Ala Phe 1580 1585 1590tta cac gca gga cag gaa ttt ggt cgt aca aag caa tgg aga gca cct 5067Leu His Ala Gly Gln Glu Phe Gly Arg Thr Lys Gln Trp Arg Ala Pro 1595 1600 1605gca acg gag gca ccg tac aag tct acg tat atg aca gat gct gat ggc 5115Ala Thr Glu Ala Pro Tyr Lys Ser Thr Tyr Met Thr Asp Ala Asp Gly1610 1615 1620 1625aat ccg ttc gtg tat cca tat ttc atc cac gat tcc tat gat tcc tcg 5163Asn Pro Phe Val Tyr Pro Tyr Phe Ile His Asp Ser Tyr Asp Ser Ser 1630 1635 1640gat atc atc aat cgt ttt gat tgg gaa aaa gcg aca gat gcc gag aaa 5211Asp Ile Ile Asn Arg Phe Asp Trp Glu Lys Ala Thr Asp Ala Glu Lys 1645 1650 1655tac cct gtc aac aat gtg aca cgt gac tac acg gca ggc ttg atc gag 5259Tyr Pro Val Asn Asn Val Thr Arg Asp Tyr Thr Ala Gly Leu Ile Glu 1660 1665 1670ctg cgt cgt tca tct gat gct ttc cgt tta ggt tct cgt gaa ttg gtc 5307Leu Arg Arg Ser Ser Asp Ala Phe Arg Leu Gly Ser Arg Glu Leu Val 1675 1680 1685gat tcc aat gtg aca atg gtt gat gcc ccg gaa atc aag gag cag gat 5355Asp Ser Asn Val Thr Met Val Asp Ala Pro Glu Ile Lys Glu Gln Asp1690 1695 1700 1705ctc gtt gtt gcc tac cgc agt gtt tcg act gcc ggt gtg gag tat tac 5403Leu Val Val Ala Tyr Arg Ser Val Ser Thr Ala Gly Val Glu Tyr Tyr 1710 1715 1720aca ttc gtg aat gcg gac act tcc agt aga aca ttg acc tta ggg cag 5451Thr Phe Val Asn Ala Asp Thr Ser Ser Arg Thr Leu Thr Leu Gly Gln 1725 1730 1735gat ttg aca gag ggc gta gtg gtg gtc gat gca gaa gag gct aat gta 5499Asp Leu Thr Glu Gly Val Val Val Val Asp Ala Glu Glu Ala Asn Val 1740 1745 1750gcc ggt gta gct gag cct gct ggt ttc gaa ttg acg gca gaa ggc atc 5547Ala Gly Val Ala Glu Pro Ala Gly Phe Glu Leu Thr Ala Glu Gly Ile 1755 1760 1765aca ctt gag cca ttg act acg gtt gtc gtc cgt gta ggc gag cag gaa 5595Thr Leu Glu Pro Leu Thr Thr Val Val Val Arg Val Gly Glu Gln Glu1770 1775 1780 1785ggg aca gac ccg ggt gat ggg gac ggc gat ggc aat acg ccg cca cca 5643Gly Thr Asp Pro Gly Asp Gly Asp Gly Asp Gly Asn Thr Pro Pro Pro 1790 1795 1800ggc gac ggc gat ggc gat gga aac acg cca cca cca ggg gat ggg gat 5691Gly Asp Gly Asp Gly Asp Gly Asn Thr Pro Pro Pro Gly Asp Gly Asp 1805 1810 1815ggc gat gga aac acg cct cct cca ggc aac ggt aat ggc aat aat cca 5739Gly Asp Gly Asn Thr Pro Pro Pro Gly Asn Gly Asn Gly Asn Asn Pro 1820 1825 1830gga aca cca cca gga aag ggt gga gaa aac cct ggt aaa ggc aaa aac 5787Gly Thr Pro Pro Gly Lys Gly Gly Glu Asn Pro Gly Lys Gly Lys Asn 1835 1840 1845gac aaa aca ccg cct ggc aaa ggt ggg gac aat cca ggt aag ggg aac 5835Asp Lys Thr Pro Pro Gly Lys Gly Gly Asp Asn Pro Gly Lys Gly Asn1850 1855 1860 1865aag cta cca ctt acc gca acc gga aca ctt aat tac atc ctg ttt ggt 5883Lys Leu Pro Leu Thr Ala Thr Gly Thr Leu Asn Tyr Ile Leu Phe Gly 1870 1875 1880gca ata atg ttg gtt ctt ggg acg ctg ctg tat cta ggg gtc aga aga 5931Ala Ile Met Leu Val Leu Gly Thr Leu Leu Tyr Leu Gly Val Arg Arg 1885 1890 1895aaa gca gga ttg aaa gaa aaa acc tta taaaaacaac ggaaaagtgt 5978Lys Ala Gly Leu Lys Glu Lys Thr Leu 1900 1905ggcaggggaa tatcccgcca cactttttcg ttattataag gcattatttg cttgtagatt 6038aaggattcgc tataggttat tttgtgtaac gtacattact tttccgttgg gccatattta 6098ttttccatac cgctcatttt tcttttccat tgggaccaca ttta 6142 2 1938 PRT Bacillus sp. 2Met Lys Lys Arg Phe Gln Arg Gly Met Ala Gly Leu Leu Ser Ile Leu -30 -25 -20Leu Ile Val Ser Met Phe Ala Gly Tyr Leu Pro Ala Arg Ala Ala Ala -15 -10 -5 -1Glu Thr Gly Asp Lys Arg Ile Glu Phe Ser Tyr Glu Arg Pro Asp Gly 1 5 10 15Asn Tyr Glu Gly Trp Asn Leu Trp Val Trp Gly Thr Gly Val Lys Asp 20 25 30Asp Gln Ile Asp Phe Thr Glu Phe Lys Glu Gly Lys Ala Tyr Ala Asp 35 40 45Ile Ala Val Ser Asp Asn Ala Asp Lys Val Gly Phe Ile Ile Arg Lys 50 55 60Gly Asp Trp Glu Glu Lys Asp Phe Asp Gly Asp Arg Ser Ile Thr Ile 65 70 75 80Asn Lys Ile Asp Asn Ile Thr Lys Val His Val Thr Ser Gln Gln Glu 85 90 95Lys Phe Gly Gln Ile Pro Asp Gly Ser Pro Pro Val Val Ala Asp Gly 100 105 110Asn Ala Asp Phe Phe Phe Arg Asp Lys Glu Leu Tyr Ala Ala Gly Glu 115 120 125Met Asp Lys Val Glu Lys Val Glu Leu Ser Ile Leu Gly Glu Lys Tyr 130 135 140Glu Met Asn Gly Glu Pro Glu Lys Glu Arg Phe Thr Tyr Thr Leu Ser145 150 155 160Asp Leu Pro Thr Gly Glu His Glu Tyr Thr Tyr Leu Val Thr Val Asp 165 170 175Gly Gln Thr Glu Glu Val Thr Asp Pro Tyr Asn Thr Val Asp Gly Arg 180 185 190Ser Val Val Glu Tyr Val Thr Ser Asp Val Gln Val Ser Ala Ser Phe 195 200 205Ile Pro Ala Lys Val Asp Tyr Asn Gln Asn Ala Val Val Lys Val Asp 210 215 220Ile Glu Ser Glu Thr Glu Thr Lys Ile Arg Glu Met Ser Ile Asn Leu225 230 235 240Ser Glu Ile Gly Gly Lys Glu Lys Ala Thr Ile Asp Pro Ala Leu Asn 245 250 255Glu Leu Thr Val Ala Val Lys Gln Gly Val Thr Ala Gly Val Lys Asn 260 265 270Leu Pro Ile Thr Ala Ile Asp Glu Phe Gly Asn Arg His Glu Gly Ser 275 280 285Ala Thr Leu Glu Val Gln Ala Arg Thr Ile Thr Gly Glu Lys Ala Asp 290 295 300Phe Asp Trp Asp Gln Ser Val Val Tyr Phe Met Leu Thr Asp Arg Phe305 310 315 320Phe Asp Gly Asp Ser Ser Asn Asn Asp Pro His Gly Ile Gly Tyr Asp 325 330 335Thr Ser Lys Ser Gly Thr Tyr Gln Gly Gly Asp Phe Lys Gly Ile Thr 340 345 350Gln Arg Leu Asp Tyr Leu Asp Glu Leu Gly Ile Asn Thr Ile Trp Ile 355 360 365Ser Pro Val Val Asp Asn Ile Lys Phe Asp Val Arg His Ser Glu Gly 370 375 380Pro Asp Thr Pro Tyr Tyr Ala Tyr His Gly Tyr Trp Ala Asp Asn Phe385 390 395 400Gly Glu Leu Asn Pro His Phe Gly Ser Met Ala Asp Phe His Glu Met 405 410 415Ile Asp Ala Ala His Glu Arg Gly Ile Lys Ile Met Val Asp Val Val 420 425 430Leu Asn His Thr Gly Tyr Gly Leu Lys Pro Gly Asp Ser Ser Ser Val 435 440 445Ala Asn Phe Pro Thr Asp Glu Asp Arg Ala Arg Phe Asp Gly Met Leu 450 455 460Arg Asp Gly Gly Ser Gly Glu Val Arg Gly Glu Leu Ala Gly Leu Pro465 470 475 480Asp Phe Leu Thr Glu Asn Pro Asp Val Arg Glu Gln Val Val Gln Trp 485 490 495Gln Thr Asp Trp Ile Glu Lys Ser Arg Thr Ala Lys Gly Asn Thr Ile 500 505 510Asp Tyr Phe Arg Val Asp Thr Val Lys His Val Glu Asp Thr Thr Trp 515 520 525Met Ala Phe Lys Asn Ala Leu Thr Lys Ala Met Pro Glu His Lys Leu 530 535 540Ile Gly Glu Ala Trp Gly Ala Asn Val Asn Asp Asp Leu Gly Tyr Leu545 550 555 560Asn Ser Gly Met Met Asp Ser Leu Leu Asp Phe Asp Phe Lys Asn Tyr 565 570 575Ala Arg Asp Phe Ala Asn Gly Gln Leu Asp Ala Val Gln Gln Lys Leu 580 585 590Glu Ala Arg Asn Ser Lys Leu Asn Asn Thr Ala Thr Leu Gly Gln Phe 595 600 605Leu Gly Ser His Asp Glu Asp Arg Phe Tyr Glu Val Val Glu Gly Asp 610 615 620Leu Gly Lys Tyr Gln Val Ala Ala Ser Leu Gln Leu Thr Ala Lys Gly625 630 635 640Gln Pro Val Ile Tyr Tyr Gly Glu Glu Leu Gly Leu Pro Gly Lys Asn 645 650 655Asp Tyr Pro Tyr Tyr Thr Asn Arg Gln Asn Met Pro Trp Asp Asp Val 660 665 670Asp Gly Asn Glu Ile Leu Glu His Tyr Gln Lys Leu Leu Ala Phe Arg 675 680 685Asn Asp Asn Pro Asn Thr Phe Ala Lys Gly Asp Arg Lys Lys Val Ala 690 695 700Gly Ser Asp Ser Glu Gly Tyr Leu Leu Phe Ser Arg Thr Tyr Gly Glu705 710 715 720Asn Ser Val Tyr Val Gly Leu Asn Thr Glu Ala Ala Ala Lys Asp Val 725 730 735Thr Leu Asn Phe Gly Ser Ser Glu Ala Val Val Thr Asp Arg Tyr Ser 740 745 750Gly Gln Glu Tyr Gln Ala Asn Glu Glu Gly Gln Val Thr Phe Ser Ile 755 760 765Pro Ala Met Glu Asp Gly Gly Thr Val Leu Leu Glu Val Glu Asn Gly 770 775 780Ala Val Pro Pro Val Glu Glu Glu Pro Thr Glu Pro Gly Glu Ile Glu785 790 795 800Glu Asn Thr Leu Arg Ile His Tyr Gln Arg Thr Asp Asn Ser Tyr Glu 805 810 815Asn Leu Gly Leu Trp Leu Trp Gly Asp Val Ala Ala Pro Ser Glu Asn 820 825 830Trp Pro Ser Gly Gly Thr Pro Phe Gln Ala Gly Asn Val Thr Asp Tyr 835 840 845Gly Ala Tyr Val Asp Val Glu Leu Ala Glu Asp Ala Gln Asn Ile Gly 850 855 860Phe Leu Val Leu Asn Thr Thr Asn Gly Asp Lys Asp Gly Gly Asp Lys865 870 875 880Ala Val Glu Leu Phe Ser Pro Asp Leu Asn Glu Ile Trp Ile Lys Gln 885 890 895Gly Ser Asp Glu Val Phe Leu Tyr Glu Pro Val Asp Leu Pro Ala Asn 900 905 910Thr Val Arg Ile His Tyr Glu Arg Thr Asn Ala Asp Tyr Glu Gly Trp 915 920 925Gly Leu Trp Asn Trp Glu Asp Val Glu Ser Pro Ser Asp Gly Trp Pro 930 935 940Asn Gly Ala Ala Asp Ala Ala Gly Ile Gly Lys Tyr Gly Ala Tyr Tyr945 950 955 960Asp Ile Lys Leu Lys Glu Asp Ala Asn Lys Ile Gly Phe Leu Phe Val 965 970 975Asn Lys Gln Ser Gly Gly Gln Thr Gly Asp Met Thr Phe Asp Met Leu 980 985 990Lys Gln Tyr Asn Gln Leu Phe Val Lys Glu Gly Glu Asp Lys Val Tyr 995 1000 1005Thr Asn Pro Tyr Gly Thr Val Pro Leu Ala Leu Val Ser Gly Glu Val 1010 1015 1020Leu Ser Asp Lys Leu Ile Ser Leu Thr Phe Thr Arg Thr Glu Gly Leu025 1030 1035 1040Asp Leu Glu Glu Leu Lys Glu Gln Leu Glu Ile Lys Asp Val Asp Gly 1045 1050 1055Asn Asp Val Ser Phe Thr Asp Val Thr Ile Glu Gly Glu Lys Thr Val 1060 1065 1070His Val His Gly Glu Phe Asp Leu Glu Lys Ile Pro Phe Ser Val Thr 1075 1080 1085Tyr Leu Asp Arg Thr Ile Ser Val Lys Ser Gly Trp Lys Leu Ile Asp 1090 1095 1100Glu Met Tyr Ala Tyr Asp Gly Lys Leu Gly Ala Glu Leu His Glu Asp105 1110 1115 1120Gly Thr Ala Thr Leu Lys Val Trp Ser Pro Lys Ala Asp Asn Val Ser 1125 1130 1135Val Val Leu Tyr Asp Lys Val Asp Gln Asn Glu Val Val Asp Thr Ile 1140 1145 1150Glu Met Val Lys Gly Asp Arg Gly Val Trp Ser Val Lys Leu Thr Lys 1155 1160 1165Asp Asn Thr Gly Leu Asp Ser Leu Lys Gly Tyr Tyr Tyr His Tyr Glu 1170 1175 1180Ile Thr His Gly Asp Val Thr Asn Leu Ala Leu Asp Pro Tyr Ala Lys185 1190 1195 1200Ser Met Ala Ala Trp Asn Asn Glu Ala Gly Asp Lys Val Gly Lys Ala 1205 1210 1215Ala Ile Val Asp Ile Gly Ser Ile Gly Pro Glu Leu Asp Tyr Ala Asp 1220 1225 1230Ile Pro Gly Phe Glu Lys Arg Glu Asp Thr Ile Ile Tyr Glu Val His 1235 1240 1245Val Arg Asp Phe Thr Ser Asp Pro Asn Ile Gly Glu Asp Leu Lys Ala 1250 1255 1260Gln Phe Gly Thr Phe Ala Ser Phe Val Glu Lys Leu Asp Tyr Ile Gln265 1270 1275 1280Glu Leu Gly Val Thr His Ile Gln Leu Leu Pro Val Met Ser Tyr Tyr 1285 1290 1295Phe Ser Asn Glu Phe Glu Ser Gly Glu Arg Met Leu Glu Tyr Ala Ser 1300 1305 1310Thr Gly Thr Asn Tyr Asn Trp Gly Tyr Asp Pro His Asn Tyr Phe Ser 1315 1320 1325Leu Ser Gly Met Tyr Ser Glu Asn Pro Glu Asp Pro Glu Leu Arg Ile 1330 1335 1340Lys Glu Phe Lys Asn Leu Ile Asn Glu Ile His Lys Arg Asp Met Gly345 1350 1355 1360Val Val Leu Asp Val Val Phe Asn His Thr Ala Gln Val His Ile Phe 1365 1370 1375Glu Asp Leu Val Pro Asn Tyr Tyr His Phe Met Asp Ala Asp Gly Thr 1380 1385 1390Pro Arg Thr Ser Phe Gly Gly Gly Arg Leu Gly Thr Thr His Glu Met 1395 1400 1405Ser Arg Arg Val Leu Val Asp Ser Ile Lys His Trp Val Asp Glu Tyr 1410 1415 1420Lys Val Asp Gly Phe Arg Phe Asp Met Met Gly Asp His Asp Ala Glu425 1430 1435 1440Ser Ile Gln Ile Ala Phe Asp Glu Ala Lys Lys Leu Asn Pro Asn Ile 1445 1450 1455Val Met Ile Gly Glu Gly Trp Val Thr Phe Ala Gly Asp Glu Gly Glu 1460 1465 1470Pro Val Gln Ala Ala Asp Gln Gln Trp Met Gln Tyr Thr Glu Ala Val 1475 1480 1485Gly Ser Phe Ser Asp Glu Phe Arg Asn Glu Leu Lys Ser Gly Phe Gly 1490 1495 1500Ser Glu Gly Gln Pro Arg Phe Ile Thr Gly Gly Ala Val Asn Val Gln505 1510 1515 1520Gln Ile Phe Asp Asn Ile Lys Ala Gln Pro His Asn Phe Met Ala Asp 1525 1530 1535Gln Pro Gly Asp Val Val Gln Tyr Ile Glu Ala His Asp Asn Leu Thr 1540 1545 1550Leu Tyr Asp Val Ile Ala Gln Ser Ile Lys Lys Asp Pro Glu Ile Ala 1555 1560 1565Glu Asn Asp Leu Glu Ile His Lys Arg Ile Arg Val Gly Asn Ala Met 1570 1575 1580Val Leu Thr Ser Gln Gly Thr Ala Phe Leu His Ala Gly Gln Glu Phe585 1590 1595 1600Gly Arg Thr Lys Gln Trp Arg Ala Pro Ala Thr Glu Ala Pro Tyr Lys 1605 1610 1615Ser Thr Tyr Met Thr Asp Ala Asp Gly Asn Pro Phe Val Tyr Pro Tyr 1620 1625 1630Phe Ile His Asp Ser Tyr Asp Ser Ser Asp Ile Ile Asn Arg Phe Asp 1635 1640 1645Trp Glu Lys Ala Thr Asp Ala Glu Lys Tyr Pro Val Asn Asn Val Thr 1650 1655 1660Arg Asp Tyr Thr Ala Gly Leu Ile Glu Leu Arg Arg Ser Ser Asp Ala665 1670 1675 1680Phe Arg Leu Gly Ser Arg Glu Leu Val Asp Ser Asn Val Thr Met Val 1685 1690 1695Asp Ala Pro Glu Ile Lys Glu Gln Asp Leu Val Val Ala Tyr Arg Ser 1700 1705 1710Val Ser Thr Ala Gly Val Glu Tyr Tyr Thr Phe Val Asn Ala Asp Thr 1715 1720 1725Ser Ser Arg Thr Leu Thr Leu Gly Gln Asp Leu Thr Glu Gly Val Val 1730 1735 1740Val Val Asp Ala Glu Glu Ala Asn Val Ala Gly Val Ala Glu Pro Ala745 1750 1755 1760Gly Phe Glu Leu Thr Ala Glu Gly Ile Thr Leu Glu Pro Leu Thr Thr 1765 1770 1775Val Val Val Arg Val Gly Glu Gln Glu Gly Thr Asp Pro Gly Asp Gly 1780 1785 1790Asp Gly Asp Gly Asn Thr Pro Pro Pro Gly Asp Gly Asp Gly Asp Gly 1795 1800 1805Asn Thr Pro Pro Pro Gly Asp Gly Asp Gly Asp Gly Asn Thr Pro Pro 1810 1815 1820Pro Gly Asn Gly Asn Gly Asn Asn Pro Gly Thr Pro Pro Gly Lys Gly825 1830 1835 1840Gly Glu Asn Pro Gly Lys Gly Lys Asn Asp Lys Thr Pro Pro Gly Lys 1845 1850 1855Gly Gly Asp Asn Pro Gly Lys Gly Asn Lys Leu Pro Leu Thr Ala Thr 1860 1865 1870Gly Thr Leu Asn Tyr Ile Leu Phe Gly Ala Ile Met Leu Val Leu Gly 1875 1880 1885Thr Leu Leu Tyr Leu Gly Val Arg Arg Lys Ala Gly Leu Lys Glu Lys 1890 1895 1900Thr Leu1905 3 833 PRT Bacillus sp. 3Met Lys Lys Arg Phe Gln Arg Gly Met Ala Gly Leu Leu Ser Ile Leu 1 5 10 15Leu Ile Val Ser Met Phe Ala Gly Tyr Leu Pro Ala Arg Ala Ala Ala 20 25 30Glu Thr Gly Asp Lys Arg Ile Glu Phe Ser Tyr Glu Arg Pro Asp Gly 35 40 45Asn Tyr Glu Gly Trp Asn Leu Trp Val Trp Gly Thr Gly Val Lys Asp 50 55 60Asp Gln Ile Asp Phe Thr Glu Phe Lys Glu Gly Lys Ala Tyr Ala Asp 65 70 75 80Ile Ala Val Ser Asp Asn Ala Asp Lys Val Gly Phe Ile Ile Arg Lys 85 90 95Gly Asp Trp Glu Glu Lys Asp Phe Asp Gly Asp Arg Ser Ile Thr Ile 100 105 110Asn Lys Ile Asp Asn Ile Thr Lys Val His Val Thr Ser Gln Gln Glu 115 120 125Lys Phe Gly Gln Ile Pro Asp Gly Ser Pro Pro Val Val Ala Asp Gly 130 135 140Asn Ala Asp Phe Phe Phe Arg Asp Lys Glu Leu Tyr Ala Ala Gly Glu145 150 155 160Met Asp Lys Val Glu Lys Val Glu Leu Ser Ile Leu Gly Glu Lys Tyr 165 170 175Glu Met Asn Gly Glu Pro Glu Lys Glu Arg Phe Thr Tyr Thr Leu Ser 180 185 190Asp Leu Pro Thr Gly Glu His Glu Tyr Thr Tyr Leu Val Thr Val Asp 195 200 205Gly Gln Thr Glu Glu Val Thr Asp Pro Tyr Asn Thr Val Asp Gly Arg 210 215 220Ser Val Val Glu Tyr Val Thr Ser Asp Val Gln Val Ser Ala Ser Phe225 230 235 240Ile Pro Ala Lys Val Asp Tyr Asn Gln Asn Ala Val Val Lys Val Asp 245 250 255Ile Glu Ser Glu Thr Glu Thr Lys Ile Arg Glu Met Ser Ile Asn Leu 260 265 270Ser Glu Ile Gly Gly Lys Glu Lys Ala Thr Ile Asp Pro Ala Leu Asn 275 280 285Glu Leu Thr Val Ala Val Lys Gln Gly Val Thr Ala Gly Val Lys Asn 290 295 300Leu Pro Ile Thr Ala Ile Asp Glu Phe Gly Asn Arg His Glu Gly Ser305 310 315 320Ala Thr Leu Glu Val Gln Ala Arg Thr Ile Thr Gly Glu Lys Ala Asp 325 330 335Phe Asp Trp Asp Gln Ser Val Val Tyr Phe Met Leu Thr Asp Arg Phe 340 345 350Phe Asp Gly Asp Ser Ser Asn Asn Asp Pro His Gly Ile Gly Tyr Asp 355 360 365Thr Ser Lys Ser Gly Thr Tyr Gln Gly Gly Asp Phe Lys Gly Ile Thr 370 375 380Gln Arg Leu Asp Tyr Leu Asp Glu Leu Gly Ile Asn Thr Ile Trp Ile385 390 395 400Ser Pro Val Val Asp Asn Ile Lys Phe Asp Val Arg His Ser Glu Gly 405 410 415Pro Asp Thr Pro Tyr Tyr Ala Tyr His Gly Tyr Trp Ala Asp Asn Phe 420 425 430Gly Glu Leu Asn Pro His Phe Gly Ser Met Ala Asp Phe His Glu Met 435 440 445Ile Asp Ala Ala His Glu Arg Gly Ile Lys Ile Met Val Asp Val Val 450 455 460Leu Asn His Thr Gly Tyr Gly Leu Lys Pro Gly Asp Ser Ser Ser Val465 470 475 480Ala Asn Phe Pro Thr Asp Glu Asp Arg Ala Arg Phe Asp Gly Met Leu 485 490 495Arg Asp Gly Gly Ser Gly Glu Val Arg Gly Glu Leu Ala Gly Leu Pro 500 505 510Asp Phe Leu Thr Glu Asn Pro Asp Val Arg Glu Gln Val Val Gln Trp 515 520 525Gln Thr Asp Trp Ile Glu Lys Ser Arg Thr Ala Lys Gly Asn Thr Ile 530 535 540Asp Tyr Phe Arg Val Asp Thr Val Lys His Val Glu Asp Thr Thr Trp545 550 555 560Met Ala Phe Lys Asn Ala Leu Thr Lys Ala Met Pro Glu His Lys Leu 565 570 575Ile Gly Glu Ala Trp Gly Ala Asn Val Asn Asp Asp Leu Gly Tyr Leu 580 585 590Asn Ser Gly Met Met Asp Ser Leu Leu Asp Phe Asp Phe Lys Asn Tyr 595 600 605Ala Arg Asp Phe Ala Asn Gly Gln Leu Asp Ala Val Gln Gln Lys Leu 610 615 620Glu Ala Arg Asn Ser Lys Leu Asn Asn Thr Ala Thr Leu Gly Gln Phe625 630 635 640Leu Gly Ser His Asp Glu Asp Arg Phe Tyr Glu Val Val Glu Gly Asp 645 650 655Leu Gly Lys Tyr Gln Val Ala Ala Ser Leu Gln Leu Thr Ala Lys Gly 660 665 670Gln Pro Val Ile Tyr Tyr Gly Glu Glu Leu Gly Leu Pro Gly Lys Asn 675 680 685Asp Tyr Pro Tyr Tyr Thr Asn Arg Gln Asn Met Pro Trp Asp Asp Val 690 695 700Asp Gly Asn Glu Ile Leu Glu His Tyr Gln Lys Leu Leu Ala Phe Arg705 710 715 720Asn Asp Asn Pro Asn Thr Phe Ala Lys Gly Asp Arg Lys Lys Val Ala 725 730 735Gly Ser Asp Ser Glu Gly Tyr Leu Leu Phe Ser Arg Thr Tyr Gly Glu 740 745 750Asn Ser Val Tyr Val Gly Leu Asn Thr Glu Ala Ala Ala Lys Asp Val 755 760 765Thr Leu Asn Phe Gly Ser Ser Glu Ala Val Val Thr Asp Arg Tyr Ser 770 775 780Gly Gln Glu Tyr Gln Ala Asn Glu Glu Gly Gln Val Thr Phe Ser Ile785 790 795 800Pro Ala Met Glu Asp Gly Gly Thr Val Leu Leu Glu Val Glu Asn Gly 805 810 815Ala Val Pro Pro Val Glu Glu Glu Pro Thr Glu Pro Gly Glu Ile Glu 820 825 830Glu 4 893 PRT Bacillus sp. 4Thr Val Pro Leu Ala Leu Val Ser Gly Glu Val Leu Ser Asp Lys Leu 1 5 10 15Ile Ser Leu Thr Phe Thr Arg Thr Glu Gly Leu Asp Leu Glu Glu Leu 20 25 30Lys Glu Gln Leu Glu Ile Lys Asp Val Asp Gly Asn Asp Val Ser Phe 35 40 45Thr Asp Val Thr Ile Glu Gly Glu Lys Thr Val His Val His Gly Glu 50 55 60Phe Asp Leu Glu Lys Ile Pro Phe Ser Val Thr Tyr Leu Asp Arg Thr 65 70 75 80Ile Ser Val Lys Ser Gly Trp Lys Leu Ile Asp Glu Met Tyr Ala Tyr 85 90 95Asp Gly Lys Leu Gly Ala Glu Leu His Glu Asp Gly Thr Ala Thr Leu 100 105 110Lys Val Trp Ser Pro Lys Ala Asp Asn Val Ser Val Val Leu Tyr Asp 115 120 125Lys Val Asp Gln Asn Glu Val Val Asp Thr Ile Glu Met Val Lys Gly 130 135 140Asp Arg Gly Val Trp Ser Val Lys Leu Thr Lys Asp Asn Thr Gly Leu145 150 155 160Asp Ser Leu Lys Gly Tyr Tyr Tyr His Tyr Glu Ile Thr His Gly Asp 165 170 175Val Thr Asn Leu Ala Leu Asp Pro Tyr Ala Lys Ser Met Ala Ala Trp 180 185 190Asn Asn Glu Ala Gly Asp Lys Val Gly Lys Ala Ala Ile Val Asp Ile 195 200 205Gly Ser Ile Gly Pro Glu Leu Asp Tyr Ala Asp Ile Pro Gly Phe Glu 210 215 220Lys Arg Glu Asp Thr Ile Ile Tyr Glu Val His Val Arg Asp Phe Thr225 230 235 240Ser Asp Pro Asn Ile Gly Glu Asp Leu Lys Ala Gln Phe Gly Thr Phe 245 250 255Ala Ser Phe Val Glu Lys Leu Asp Tyr Ile Gln Glu Leu Gly Val Thr 260 265 270His Ile Gln Leu Leu Pro Val Met Ser Tyr Tyr Phe Ser Asn Glu Phe 275 280 285Glu Ser Gly Glu Arg Met Leu Glu Tyr Ala Ser Thr Gly Thr Asn Tyr 290 295 300Asn Trp Gly Tyr Asp Pro His Asn Tyr Phe Ser Leu Ser Gly Met Tyr305 310 315 320Ser Glu Asn Pro Glu Asp Pro Glu Leu Arg Ile Lys Glu Phe Lys Asn 325 330 335Leu Ile Asn Glu Ile His Lys Arg Asp Met Gly Val Val Leu Asp Val 340 345 350Val Phe Asn His Thr Ala Gln Val His Ile Phe Glu Asp Leu Val Pro 355 360 365Asn Tyr Tyr His Phe Met Asp Ala Asp Gly Thr Pro Arg Thr Ser Phe 370 375 380Gly Gly Gly Arg Leu Gly Thr Thr His Glu Met Ser Arg Arg Val Leu385 390 395 400Val Asp Ser Ile Lys His Trp Val Asp Glu Tyr Lys Val Asp Gly Phe 405 410 415Arg Phe Asp Met Met Gly Asp His Asp Ala Glu Ser Ile Gln Ile Ala 420 425 430Phe Asp Glu Ala Lys Lys Leu Asn Pro Asn Ile Val Met Ile Gly Glu 435 440 445Gly Trp Val Thr Phe Ala Gly Asp Glu Gly Glu Pro Val Gln Ala Ala 450 455 460Asp Gln Gln Trp Met Gln Tyr Thr Glu Ala Val Gly Ser Phe Ser Asp465 470 475 480Glu Phe Arg Asn Glu Leu Lys Ser Gly Phe Gly Ser Glu Gly Gln Pro 485 490 495Arg Phe Ile Thr Gly Gly Ala Val Asn Val Gln Gln Ile Phe Asp Asn 500 505 510Ile Lys Ala Gln Pro His Asn Phe Met Ala Asp Gln Pro Gly Asp Val 515 520 525Val Gln Tyr Ile Glu Ala His Asp Asn Leu Thr Leu Tyr Asp Val Ile 530 535 540Ala Gln Ser Ile Lys Lys Asp Pro Glu Ile Ala Glu Asn Asp Leu Glu545 550 555 560Ile His Lys Arg Ile Arg Val Gly Asn Ala Met Val Leu Thr Ser Gln 565 570 575Gly Thr Ala Phe Leu His Ala Gly Gln Glu Phe Gly Arg Thr Lys Gln 580 585 590Trp Arg Ala Pro Ala Thr Glu Ala Pro Tyr Lys Ser Thr Tyr Met Thr 595 600 605Asp Ala Asp Gly Asn Pro Phe Val Tyr Pro Tyr Phe Ile His Asp Ser 610 615 620Tyr Asp Ser Ser Asp Ile Ile Asn Arg Phe Asp Trp Glu Lys Ala Thr625 630 635 640Asp Ala Glu Lys Tyr Pro Val Asn Asn Val Thr Arg Asp Tyr Thr Ala 645 650 655Gly Leu Ile Glu Leu Arg Arg Ser Ser Asp Ala Phe Arg Leu Gly Ser 660 665 670Arg Glu Leu Val Asp Ser Asn Val Thr Met Val Asp Ala Pro Glu Ile 675 680 685Lys Glu Gln Asp Leu Val Val Ala Tyr Arg Ser Val Ser Thr Ala Gly 690 695 700Val Glu Tyr Tyr Thr Phe Val Asn Ala Asp Thr Ser Ser Arg Thr Leu705 710 715 720Thr Leu Gly Gln Asp Leu Thr Glu Gly Val Val Val Val Asp Ala Glu 725 730 735Glu Ala Asn Val Ala Gly Val Ala Glu Pro Ala Gly Phe Glu Leu Thr 740 745 750Ala Glu Gly Ile Thr Leu Glu Pro Leu Thr Thr Val Val Val Arg Val 755 760 765Gly Glu Gln Glu Gly Thr Asp Pro Gly Asp Gly Asp Gly Asp Gly Asn 770 775 780Thr Pro Pro Pro Gly Asp Gly Asp Gly Asp Gly Asn Thr Pro Pro Pro785 790 795 800Gly Asp Gly Asp Gly Asp Gly Asn Thr Pro Pro Pro Gly Asn Gly Asn 805 810 815Gly Asn Asn Pro Gly Thr Pro Pro Gly Lys Gly Gly Glu Asn Pro Gly 820 825 830Lys Gly Lys Asn Asp Lys Thr Pro Pro Gly Lys Gly Gly Asp Asn Pro 835 840 845Gly Lys Gly Asn Lys Leu Pro Leu Thr Ala Thr Gly Thr Leu Asn Tyr 850 855 860Ile Leu Phe Gly Ala Ile Met Leu Val Leu Gly Thr Leu Leu Tyr Leu865 870 875 880Gly Val Arg Arg Lys Ala Gly Leu Lys Glu Lys Thr Leu 885 890 5 16 PRT Bacillus sp. 5Thr Val Pro Leu Ala Leu Val Ser Gly Glu Val Leu Ser Asp Lys Leu 1 5 10 15 6 14 PRT Bacillus sp. 6Glu Thr Gly Asp Lys Arg Ile Glu Phe Ser Tyr Glu Arg Pro 1 5 10 7 24 DNA Artificial Sequence Description of Artificial Sequence Primer 1 7ctgcaggtat cggtaaatac ggtg 24 8 24 DNA Artificial Sequence Description of Artificial Sequence Primer 2 8tgacgtaacg aatcttgctc taga 24 9 24 DNA Artificial Sequence Description of Artificial Sequence Primer 3 9tctagagcat tatcaaaaat tact 24 10 24 DNA Artificial Sequence Description of Artificial Sequence Primer 4 10ccggaactga gaatcaaaga attc 24 11 24 DNA Artificial Sequence Description of Artificial Sequence Primer 5 11gaattcggaa atcgccatga ggga 24 12 23 DNA Artificial Sequence Description of Artificial Sequence Primer 6 12gtggatggta atgaaattct aga 23 13 25 DNA Artificial Sequence Description of Artificial Sequence Primer A 13tctagatgtg caattttgcg caaac 25 14 25 DNA Artificial Sequence Description of Artificial Sequence Primer B 14aagcttgggg cagaattgca tgaag 25

Claims

1. An isolated DNA fragment encoding an amylopullulanase which exhibits both alkaline pullulanase and alkaline α-amylase activities and having a nucleotide sequence shown in SEQ ID NO:1.

2. An isolated DNA fragment encoding alkaline α-amylase, wherein said alkaline α-amylase has an amino acid sequence of SEQ ID NO:3.

3. The isolated DNA fragment of claim 1, which further comprises a nucleotide sequence capable of regulating expression of a gene.

4. A recombinant DNA comprising the DNA fragment of claim 1.

5. A transformed microorganism comprising the recombinant DNA of claim 4.

6. A method for producing alkaline amylopullulanase, alkaline α-amylase, or alkaline pullulanase, comprising culturing the transformed microorganism of claim 5 and isolating the alkaline amylopullulanase, alkaline α-amylase or alkaline pullulanase produced by the microorganism.

7. An isolated DNA fragment encoding a protein exhibiting alkaline α-amylase activity and alkaline pullulanase activity, wherein said protein has an amino acid sequence shown in SEQ ID NO:2, wherein amino acids (−32) to (−1) are deleted.

8. An isolated DNA fragment encoding a protein exhibiting alkaline α-amylase activity, wherein said protein has an amino acid sequence shown in SEQ ID NO:3, wherein amino acids 1 to 32 are deleted.