Patent Application
20210009982
This application claims the benefit under 35 USC 119(a) of Korean Patent Application No. 10-2019-0019901 filed on Feb. 20, 2019, in the Korean Intellectual Property Office, the entire disclosures of which are incorporated herein by reference for all purposes.
The present disclosure relates to an agarase-3,6-anhydro-L-galactosidase-arabinose isomerase enzyme complex and a method for producing tagatose from agar using the same. More particularly, the present disclosure relates to a method for preparing tagatose using agarooligosaccharide present in marine biomass (agar). It relates to an agarase complex consisting of agarase, 3,6-anhydro-L-galactosidase and arabinose isomerase, and a method for degrading agar and producing tagatose using the same.
Recently, marine algae having cell walls consisting of many fibrils and various polysaccharides is drawing attentions as a new raw material of bioenergy. Marine algae is advantageous in that the pretreatment process can be simplified due to low (hardly soluble) lignin content. In addition, the marine algae is composed of about 60-95% of water and other components about 50% of which are carbohydrates. The carbohydrates can be converted to monosaccharides for producing bioenergy and biochemicals.
In Korea and Japan, the red algae layer (mostly Porphyra yezoensis) is cultivated actively. Red algae accounts for more than half of the marine algae growing wild in Korea. The red algae that may be used in the present disclosure is agar. Agar is the most diverse species of red algae with superior productivity. Agar consists of about 50-70% of galactan, which is the main ingredient, as well as about 15-25% of cellulose, less than 15% or proteins and less than 7% of lipids.
If agar, which is the representative byproduct in processing and extraction of red algae, is degraded effectively, galactose or glucose useful for ethanol production can be obtained. In addition, the metabolites such as dioses, trioses, oligosaccharides, etc. produced during the degradation can be useful physiologically active substances. At present, seaweed polysaccharides such as agar and carrageenan are extracted from red algae through treatment with alkalis, acids, enzymes, etc. and are usefully used industrially as food or cosmetic additives or healthful food resources. However, because red algae has a complicated structure difficult to be degraded, there is difficulty in using it as a substrate for biofuel production. Also, there are problems in disposing of byproducts and wastes. Agarase, which is an enzyme that degrades agar, hydrolyzes β-1,4 linkages in agarose and produces neoagarooligosaccharides with galactose disaccharide or trisaccharide residues. κ-Carrageenase, which is an enzyme that degrades κ-carrageenan, breaks down the 3-,4-linkage galactose units of κ-carrageenan to produce disaccharide carrageenan residues. Agarase can be classified into α-agarase and β-agarase based on the linkage degraded by the enzyme. The α-agarase degrades the α-1,3 linkages in the galactose residues in agarose to produce agarooligosaccharides. The agarooligosaccharides are reported to have apoptosis-inducing activity, anticancer activity, antiviral activity, antioxidant activity, immunomodulatory activity, antiallergic activity, antiinflammatory activity, etc. And, the β-agarase degrades the β-1,4 linkages in the galactose residues in agarose to produce neoagarooligosaccharides. The neoagarooligosaccharides are reported to inhibit bacterial growth and have antioxidant activity, starch aging-inhibiting effect, skin-moisturizing effect, skin-whitening effect, etc.
Cellulose is one of the most abundant biomass in nature. The enzymes that degrade cellulose are produced by fibrous fungi or several bacteria. Among them, anaerobic bacteria in the class Clostridia produce enzyme complexes using domains called cohesion and dockerin. Since the enzyme complex has several cohesin domains in the scaffold protein, binding is possible with enzymes having dockerin domains. Also, the scaffold protein has a carbohydrate-binding module (CBM), which improves the efficiency of complex formation. An enzyme having the dockerin domain and capable of forming an enzyme complex is called a chimeric enzyme. By using an enzyme having a dockerin domain engineered to bind a specific cohesin domain, a complex can be formed as desired by selecting the necessary enzyme. The formed enzyme complex degrades a polysaccharide into smaller polysaccharide units, which are degraded further into smaller disaccharides or monosaccharides by the next enzyme.
Tagatose is a rare sugar contained in trace amounts in dairy products or some plants, and is used in diet food products as a low-calorie sweetener. Generally, D-tagatose is an isomer of galactose and a C4 epimer of D-fructose. It is a low-calorie sweetener which is 92% as sweet as table sugar, but with only about 30% of the calories (1.5 kcal/g). Additionally, it is a non-caloric sweetener which is hardly metabolized during the in-vivo absorption process. 15-20% of the amount of tagatose ingested is absorbed into the body, but this absorption does not affect the blood glucose level because it is due to decomposition by microorganisms in the large intestine not by human's own digestive capability. Accordingly, it is expected to provide a blood glucose level-controlling effect for diabetic patients, and is known to provide food for enteric microorganisms, thereby helping excretion. Tagatose is a healthful sweetener that can be safely included in chocolate, gums, bread, candies, etc. favored by children, instead of sugar, because it does not cause tooth decay. Therefore, it is drawing a lot of attentions as a substance that can contribute to the prevention of diseases caused by excessive sugar intake. Additionally, since tagatose has superior stability against heat and pH, with a boiling point of 134° C. and a pH of 2-7, it is not readily broken down, unlike most artificial sweeteners. It has physical and chemical properties very similar to those of sugar and is an important sugar substitute because it is a ketose exhibiting the characteristic of browning, which is very similar to that of fructose.
For these reasons, tagatose is drawing attentions as a functional sugar such as a food supplement or a diet sweetener. Therefore, there is a growing need for the development of a method for effectively producing tagatose in the food industry. It is because tagatose is a rare sugar included in trace amounts in dairy products or some plants and it cannot be synthesized chemically. It was recently reported that L-arabinose isomerase converts L-arabinose into L-ribulose and D-galactose into tagatose (patent document 1). At present, tagatose is being produced by isomerization of galactose via bioconversion using L-arabinose isomerase (patent document 2). Galactose is obtained from lactose. However, stable and consistent large-scale production is difficult because the supply and demand of lactose are unstable, lactose is more expensive than glucose or fructose, and its price varies greatly depending on the dairy market situation.
Therefore, methods for producing tagatose from glucose or fructose, which are advantageous in terms of stable supply and demand and low cost, as substrates using enzymes are being studied actively. But, the production of tagatose from fructose through a single enzyme reaction is not known yet. In addition, the conversion is hardly achieved and the production yield is very low with epimerases known thus far, as such single enzymes. Accordingly, a method for using red algae, the supply and demand of which are stable and the cost of which is low, as a substrate is necessary.
The present disclosure is directed to providing an enzyme complex which convers red algae-derived agar, as a marine biomass, into tagatose, and a method for preparing the same.
The present disclosure is also directed to providing a method for preparing tagatose by degrading red algae biomass using the enzyme complex.
In an aspect, the present disclosure provides an agarase complex wherein: 1) a fusion protein 1 in which a monosaccharide convertase and a dockerin module are bound; 2) a fusion protein 2 in which agarase and a dockerin module are bound; and 3) a fusion protein 3 in which 3,6-anhydro-L-galactosidase and a dockerin module are bound; are linked via dockerin-cohesin binding by a mini scaffold protein including a cohesin module.
The monosaccharide convertase may be Lactobacillus-derived arabinose isomerase represented by an amino acid sequence of SEQ ID NO 1, although not being limited thereto.
The dockerin may be a cellulase-derived dockerin selected from a group consisting of endo-β-1,4-glucanase B, endo-β-1,4-xylanase B and exo-glucanase S. Specifically, the dockerin may have a base sequence of SEQ ID NO 35. But, considering genetic code degeneracy, a base sequence having 80% homology, specifically 85% homology, more specifically 90% homology, most specifically 95% homology, to the base sequence of SEQ ID NO 3 may also be included in the base sequence of the dockerin of the present disclosure, although not being limited thereto.
The agarase may be an agarase derived from one selected from a group consisting of Pseudomonas, Saccharophagus and Aleromonas, although not being limited thereto. More specifically, the agarase may be β-agarase, specifically one having a base sequence of SEQ ID NO 26. But, considering genetic code degeneracy, a base sequence having 80% homology, specifically 85% homology, more specifically 90% homology, most specifically 95% homology, to the base sequence of SEQ ID NO 26 may also be included in the base sequence of the β-agarase of the present disclosure, although not being limited thereto.
Specifically, the 3,6-anhydro-L-galactosidase may be derived from Zobellia and may have a base sequence of SEQ ID NO 36. But, considering genetic code degeneracy, a base sequence having 80% homology, specifically 85% homology, more specifically 90% homology, most specifically 95% homology, to the base sequence of SEQ ID NO 36 may also be included in the base sequence of the 3,6-anhydro-L-galactosidase of the present disclosure, although not being limited thereto.
The mini scaffold protein may be one selected from a group consisting of mini cellulose-binding protein A (mCbpA), Clostridium thermocellulm-derived mini scaffold protein (mCipA) and Clostridium cellulolyticum-derived mini scaffold protein (mCipC). More specifically, it may be mini cellulose-binding protein A (mCbpA) having a base sequence of SEQ ID NO 17. But, considering genetic code degeneracy, a base sequence having 80% homology, specifically 85% homology, more specifically 90% homology, most specifically 95% homology, to the base sequence of SEQ ID NO 17 may also be included in the base sequence of the mini cellulose-binding protein A (mCbpA) of the present disclosure, although not being limited thereto.
The enzyme complex may be agarase-3,6-anhydro-L-galactosidase-arabinose isomerase or β-agarase-3,6-anhydro-L-galactosidase-arabinose isomerase, although not being limited thereto.
In another aspect, the present disclosure provides a method for producing tagatose by degrading biomass using the agarase complex.
The biomass may be agar selected from purified agar, red algae-derived agar or agar present in red algae, although not being limited thereto.
In another aspect, the present disclosure provides a method for preparing an agarase complex, which includes: (a) a step of preparing a fusion protein 1 by linking a dockerin module to arabinose isomerase; (b) a step of preparing a fusion protein 2 by linking a dockerin module to β-agarase; (c) a step of preparing a fusion protein 3 by linking a dockerin module to 3,6-anhydro-L-galactosidase; (d) a step of preparing a mini scaffold protein having a cohesin module; and (e) a step of preparing an agarase complex by binding the cohesin module to the dockerin modules by quantifying the fusion proteins 1-3 and the mini scaffold protein of the step (d) to the same concentration of 2-20 nmol, more specifically 10 nmol, and the same proportion (1:1:1:1) and mixing them in a binding solution comprising 25 mM calcium chloride (CaCl2)) and conducting reaction at 4° C. for 24 hours.
In the step (e), if the concentration of the fusion proteins and the mini scaffold protein is lower than 2 nmol or higher than 20 nmol, or if they are mixed with different proportions, the binding efficiency of the dockerin modules and the cohesin module is low.
In the present disclosure, “endoglucanase” refers to an enzyme which catalyzes the production of glucose polymers (cellobiose, cellotriose, etc.) by hydrolyzing the β-1,4-D-glycosidic bond of cellulose, and includes the enzyme endo-β-1,4-glucanase (EC 3.2.1.4, endoglucanase).
In the present disclosure, “cellulose-binding protein A” is a protein derived from Clostridium cellulovorans, and is a scaffold protein forming a cellulosome. Since the cellulose-binding protein has a carbohydrate-binding module which recognizes cellulose and binds strongly thereto, it allows easy access to a carbohydrate or cellulose for an enzyme binding to the protein. The cellulose-binding protein has a cohesin domain which binds specifically to the dockerin domain possessed by the enzyme of cellulosome-producing bacteria. Therefore, the number of the binding enzymes is determined by the number of cohesins.
In the present disclosure, the dockerin module of a bacterium in the genus Clostridium refers to a module possessed by a cellulosomal cellulase protein which forms the enzyme complex cellulosome through interaction with a cohesin module which is a portion of the cellulose-binding protein of a bacterium in the genus Clostridium.
In the present disclosure, “dockerin-cohesin binding” refers to the binding between the dockerin module of a cellulosome-forming enzyme and the cohesin module of a scaffold protein during the process whereby a cellulosome capable of degrading cellulose is formed (Bayer et al. Annual Review of Microbiol, 2004, 58, 521-554).
In the present disclosure, for the dockerin-cohesin binding, type I dockerin and cohesion of a strain producing a cellulosome may be used without limitation. Specifically, those derived from the same species may be used when considering species specificity. For example, dockerin type I derived from Clostridium cellulovorans, such as EngH, EngK, ExgS, EngL, ManA, EngM and EngN, and cohesin type I of cbpA derived from Clostridium cellulovorans may be used, although not being limited thereto.
In the present disclosure, a “vector” refers to a gene construct including an essential regulatory element operably linked so that the gene construct can be expressed as a target protein in a suitable host cell. When the vector is a replicable expression vector, it may include a replication origin which is a specific nucleic acid sequence at which replication is initiated.
In general, a plasmid vector is an extra-chromosomal circular double-stranded DNA, which is present in a cell and has various functions. It produces antibiotic-resistant substances and bacteriocins, thereby acting as an inhibitor to kill bacteria or host cells, and performs physiological functions such as pigment formation, compound decomposition and nitrogen fixation. It has a restriction enzyme site for insertion of foreign DNA fragments of up to about 10 kb in length.
The vector according to the present disclosure may contain a selection marker. The selection marker is for selecting cells transfected with the vector. Markers for conferring selectable phenotypes such as drug resistance, nutritional requirement, and resistance to cytotoxic agents or expression of surface proteins may be used. Under the environment treated with a selective agent, the transformed cells can be selected because only the cells expressing the selection marker survive. Representative examples of the selection marker include auxotrophic markers ura4, leu1, his3, etc. However, the types of the marker that can be used in the present disclosure are not limited to those examples.
The vector related with the present disclosure includes a plasmid vector (e.g., pSC101, ColE1, pBR322, pUC8/9, pHC79, pUC19, etc.), a cosmid vector, a bacteriophage vector (e.g., gt4B, -Charon, z1, M13, etc.), a viral vector, etc., although not being limited thereto.
A plasmid used as a vector and capable of inserting relatively small DNA fragments only, which is the major drawback of a bacteriophage, can clone larger DNA fragments using a cosmid, which is a manipulated hybrid of a plasmid and a phage DNA.
There is a cos site which is packed into a phage particle, and it has a gene that can select the plasmid and the start point of replication of the plasmid replicated in the bacterial host. Like a bacteriophage vector, it is packed in a protein envelope in vitro. But, once the packed DNA has infected the E. coli host cell, the DNA is replicated in the plasmid form rather than the bacteriophage DNA and is not lysed. Its size is 2.5 kb. After the host cell has been infected and packaged and the cos site has been split from 37 kb to 52 kb, a foreign DNA is housed as an insert. Generally, 35-45 kb can be cloned into a cosmid vector.
A phage, which is a common form of the bacteriophage vector, originates from a 50-kb double-stranded wild-type genome with cohesive termini or cos with complementary ends of single-stranded 12 nucleotides capable of forming base pairs. In the lytic pathway, new viruses are replicated in the host cell, and the host cell is lysed after the offspring viruses are released. This type of DNA accommodates up to 5% of the genome, i.e., 3 kb of its total 52 kb, and a vector that creates a space for foreign DNA is free of non-essential DNA fragments.
The viral vector may be a vector derived from a retrovirus, e.g., human immunodeficiency virus (HIV), murine leukemia virus (MLV), avian sarcoma and leukosis virus (ASLV), spleen necrosis virus (SNV), Rous sarcoma virus (RSV), mouse mammary tumor virus (MMTV), etc., adenovirus, an adeno-associated virus (AAV), herpes simplex virus, etc., although not being limited thereto.
In the present disclosure, a “primer” refers to a single-stranded oligonucleotide. It includes a ribonucleotide and may be specifically a deoxyribonucleotide. The primer is hybridized or annealed to a portion of a template to form a double-stranded structure. In the present disclosure, a primer may be hybridized or annealed to an NGS adapter sequence. The annealing refers to apposition of an oligonucleotide or a nucleic acid to a template nucleic acid, and the apposition refers to formation of a nucleic acid molecule complementary to the template nucleic acid or a part thereof by polymerization of nucleotides using a polymerase. The hybridization refers to formation of a duplex structure by pairing of two single-stranded nucleic acids with complementary base sequences. The primer may serve as a starting point of synthesis under conditions for inducing the synthesis of an elongated product of the primer complementary to the template.
In the present disclosure “operably linked” means that a nucleotide sequence encoding a target protein is linked in such a way as to perform general functions. The operable linkage to a recombinant vector may be achieved using a genetic recombination technique well known in the art, and site-specific DNA cleavage and ligation may be easily achieved using enzymes generally known in the art.
In the present disclosure, the “regulatory element” refers to an undecoded nucleic acid sequence that helps to improve the transcription, translation or expression of a nucleic acid sequence encoding a protein or affects the same. The expression vector of the present disclosure necessarily includes the genetic circuit of the present disclosure as the regulatory element, and may include an expression control sequence that may affect protein expression, e.g., a start codon, a stop codon, a polyadenylation signal, an enhancer, a signal sequence for membrane targeting or secretion, etc.
In the present disclosure, the “host cell” refers to a cell which parasitizes another microorganism or gene and supplies nutrition thereto, and means a cell in which a vector is transformed into the host cell to exert various genetic or molecular effects in the host cell. A foreign DNA such as a vector may be inserted into the host cell when the cell is in a competent state capable of accepting the foreign DNA. When a vector is successfully introduced into a host cell, the genetic trait of the vector is provided to the host cell.
Specifically, the host microorganism of the present disclosure may be Gram-negative bacteria. The Gram-negative bacteria include bacteria in the genus Salmonella (Salmonella sp.), the genus Acinebacter (Acinebacter sp.), the genus Escherichia (Escherichia sp.), the genus Pseudomonas (Pseudomonas sp.), the genus Klebsiella (Klebsiella sp.), etc., e.g., Salmonella typhimurium, Acinebacter calcoaceticus, E. coli, Pseudomonas aeruginosa, Klebsiella aerogenes, Acinetobacter baumannii, Klebsiella pneumoniae, etc. However, the host cell that can be transformed with the vector of the present disclosure is not limited to those described above.
Transformation can be used to introduce a vector into a host cell. The “transformation” refers to a phenomenon in which DNA is introduced into a host and the DNA becomes replicable as a factor of chromosome or by chromosomal integration. The introduction of the foreign DNA into the cell results in artificial genetic change. Any transformation method can be used for the transformation according to common methods in the art. In general, the transformation method includes CaCl2) precipitation, the Hanahan method in which the effect of the CaCl2) method is improved by using DMSO (dimethyl sulfoxide), electroporation, calcium phosphate precipitation, protoplast fusion, agitation using silicon carbide fibers, Agrobacteria-mediated transformation, transformation using polyethylene glycol (PEG), dextran sulfate-, lipofectamine- and drying/inhibition-mediated transformation, etc. The method for transforming the plasmid of the present disclosure is not limited to the above examples, and the transformation methods commonly used in the art can be used without limitation.
The host cell transformed by the above-described method can be cultured as necessary via culturing methods commonly used in the art, and the culture medium and culturing period can be selected as desired by those skilled in the art.
Specifically, E. coli cultured in an LB (Luria-Bertani) medium for 8 hours may be cultured further for 12 hours to induce the production of proteins from recombinant genes. As the medium, various media that can be generally used in the art may be used.
A method for producing tagatose according to the present disclosure is environment-friendly because only an enzyme obtained from a microorganism is used, and the production efficiency can be maximized whereas the production cost is reduced greatly because only a simple process of enzyme complex formation is necessary and an inexpensive biomass substrate is used. That is to say, by using the enzyme complex according to the present disclosure, agar obtained from the marine biomass red algae can be degraded effectively and galactose obtained as a degradation product can be converted into tagatose, which is a useful rare sugar, effectively.
Hereinafter, the present disclosure will be described in detail through examples. However, the following examples are for illustrative purposes only and it will be apparent to those of ordinary skill in the art that the scope of the present disclosure is not limited by the examples.
In order to prepare a novel enzyme complex, a vector and a transformant including genes encoding the components of the enzyme complex were prepared.
1.1 Lactobacillus-Derived Arabinose Isomerase Expression Vector
For cloning of proteins for producing tagatose from an agar degradation product as a substrate, a vector expressing the arabinose isomerase gene was prepared first.
Referring to the base sequence of the arabinose isomerase (LsAraA) gene from the gDNA of bacteria in the genus Lactobacillus, primers were designed and synthesized such that the Sac I recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 2) and the Hind III recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 3). Then, PCR was conducted using the synthesized primers. As a result, the PCR band of the 1479-bp arabinose isomerase (LsAraA) gene (SEQ ID NO 4) was observed (result not shown).
Then, the arabinose isomerase (LsAraA) gene was purified, ligated to the E. coli expression vector pColdII, and transformed into E. coli BL21 using the restriction enzymes Sac I and Hind III. The transformant was named BL21/LsAraA. Then, the ligated recombinant plasmid DNA was isolated from the transformant. The recombinant plasmid vector was named pColdII LsAraA.
1.2 Preparation of Lactobacillus-Derived Arabinose Isomerase Expression Vector and Transformant Fused with Dockerin
An expression vector and a transformant wherein the arabinose isomerase enzyme of Example 1.1 was fused with a cellulase-derived dockerin domain were prepared.
A. Arabinose Isomerase Gene Fragment
Referring to the base sequence of the arabinose isomerase (LsAraA) gene from the genomic DNA of bacteria in the genus Lactobacillus, primers were designed and synthesized such that the Sac I recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 5) and the 10-bp sequence at the N-terminal of the dockerin moiety of the endo-β-1,4-glucanase B gene derived from Clostridium cellulovorans was inserted to the 5′ end of a reverse primer (SEQ ID NO 6). Then, PCR was conducted using the synthesized primers. As a result, the PCR bands of the Sac I recognition sequence capable of recognizing the dockerin moiety and the 1521-bp arabinose isomerase (LsAraA) gene were observed (result not shown).
B. Dockerin Fragment
In addition, referring to the base sequence of the dockerin moiety of the endo-β-1,4-glucanase B gene from the gDNA of Clostridium cellulovorans, primers were designed and synthesized such that the 10-bp sequence at the C-terminal of the arabinose isomerase (LsAraA) gene was inserted to the 5′ end of a forward primer (SEQ ID NO 7) and the Kpn I recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 8).
The 10-bp sequence at the N-terminal of the dockerin moiety of the endo-β-1,4-glucanase B gene is represented by SEQ ID NO 9, and the 10-bp sequence at the C-terminal of the arabinose isomerase (LsAraA) gene is represented by SEQ ID NO 10.
Then, PCR was conducted using the synthesized primers. As a result, the PCR band of the dockerin moiety of the 195-bp endo-β-1,4-glucanase B gene (SEQ ID NO 11) was observed.
C. Preparation of Fusion Protein Expression Vector and Transformant
The gene amplification product of the arabinose isomerase (LsAraA) gene and the dockerin domain of cellulase obtained above was subjected to electrophoresis on 0.8% agarose gel, and the DNA fragments on the agarose gel were recovered using a gel extraction kit (GeneAll).
Using the two recovered DNA fragments, primers were designed and synthesized such that the Sac I recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 12) and the Kpn I recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 13).
Then, overlap PCR was conducted using the recovered DNA fragments in order to link the arabinose isomerase (LsAraA) gene with the dockerin domain of cellulase. The overlap PCR reaction was conducted at 94° C. for 2 minutes followed by 10 cycles of 94° C. for 30 seconds, 52° C. for 25 minutes and 72° C. for 5 minutes, finally at 72° C. for 5 minutes. As a result of the PCR, a PCR band of the bacterium-derived expansin gene linked with the 1671-bp dockerin domain of cellulase (SEQ ID NO 14) was observed (result not shown).
After purifying the dockerin-fused arabinose isomerase LsAraA Doc gene, a recombinant expression vector was prepared by ligating the SacI and KpnI restriction enzyme sequences to the E. coli expression vector pColdII. Then, a transformant was prepared by transforming E. coli BL21 with the expression vector. Then, the plasmid DNA of the ligated recombinant expression vector was isolated from the transformant. The recombinant vector was named pColdII LsAraA-Doc (
1.3 Confirmation of Expression of Novel Enzyme Complex in Transformant
In order to investigate protein expression in the transformant obtained in Example 1, purification and SDS-PAGE were performed using His-Tag.
Expression was induced in the E. coli transformant with IPTG at 16° C. for 12 hours using 1 mM IPTG. After creating a condition where the arabinose isomerase enzyme and the dockerin-fused arabinose isomerase enzyme can be expressed, the cells were cultured at 16° C. for 12 hours under shaking and then centrifuged. The cells were lysed by sonication and then centrifuged. Proteins obtained by concentrating the supernatant (Millipore, Amicon 10 kDa cutoff) was loaded onto SDS-PAGE. Then, the proteins were analyzed by western blot using the His-tag attached at the N-terminal. As a result, the arabinose isomerase enzyme and the dockerin-fused arabinose isomerase enzyme were observed at the expected locations (
2.1 Construction of Expression Vector for Enzyme Complex
For cloning of the mini cellulose-binding protein A gene having a cellulose-binding module (CBM) and two cohesin modules of cellulose-binding protein A which is the primary scaffolding subunit of Clostridium cellulovorans, primers were synthesized such that the BamHl recognition sequence (ggatcc) was inserted to the 5′ end of a forward primer (SEQ ID NO 15) and the XhoI recognition sequence (ctcgag) was inserted to the 5′ end of a reverse primer (SEQ ID NO 16) referring to the base sequence. As a result, a 1659-bp PCR band containing the mCbpA gene (SEQ ID NO 17) which is a part of the cellulose-binding protein A gene derived from Clostridium cellulovorans was observed (result not shown).
2.2 Confirmation of Enzyme Complex Formation
In order to confirm the formation of a complex through binding between the arabinose isomerase linked with the dockerin module of the endo-β-1,4-glucanase B gene and the mini cellulose-binding protein mCbpA, the two proteins were mixed and incubated at low temperature and then incubated to induce complex formation. For the complex formation, the mini scaffold protein and the arabinose isomerase were quantitated both to 10 nmol and then mixed in a binding solution containing 25 mM CaCl2). For binding between the cohesin module and the dockerin module, reaction was conducted at 4° C. for 24 hours.
The formation of a complex through binding between the arabinose isomerase enzyme linked with the dockerin module of the endo-β-1,4-glucanase B gene and the mini cellulose-binding protein mCbpA was confirmed by measuring increased tagatose conversion activity. As a result of measuring tagatose conversion activity for mCbpA, arabinose isomerase and arabinose isomerase-mCbpA using galactose as a substrate, the degradation activity was increased in the order of mCbpA (M), arabinose isomerase (LsAraA, L) and arabinose isomerase-mCbpA (LM) (
In addition, since the fusion protein with the mini cellulose-binding protein mCbpA showed higher tagatose conversion activity than arabinose isomerase (LsAraA) alone, it was confirmed that mCbpA improves the tagatose conversion activity of arabinose isomerase (LsAraA).
For production of tagatose from the less expensive substrate agar, a fusion protein including agarase and dockerin and a fusion protein including 3,6-anhydro-L-galactosidase and dockerin were designed.
3.1 Preparation of Enzyme Complex (Fusion of β-Agarase and Dockerin)
A. Isolation of β-Agarase Gene
In order to bind β-agarase to the dockerin gene, primers for processing both ends of the β-agarase gene were prepared. Primers were designed and synthesized such that the Sac I recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 18) and the referring to the base sequence of the β-agarase AgaB gene from the genomic DNA of bacteria in the genus Zobellia and a 10-bp sequence at the N-terminal was inserted to the 5′ end of a reverse primer (SEQ ID NO 19) referring to the base sequence of the dockerin moiety of the endo-β-1,4-glucanase B gene derived from Clostridium cellulovorans. Then, PCR was conducted using the synthesized primers. The PCR reaction was conducted at 95° C. for 5 minutes, followed by 30 cycles of 95° C. for 1 minute, 52° C. for 1 minute and 72° C. for 2 minutes, finally at 72° C. for 5 minutes. As a result, a 1005-bp PCR band containing the β-agarase gene (SEQ ID NO 20) was observed (result not shown).
B. Processing of β-Agarase Gene
Referring to the base sequence of the dockerin moiety of the endo-β-1,4-glucanase B gene from the gDNA of Clostridium cellulovorans, primers were designed and synthesized such that a 10-bp sequence at the C-terminal of the β-agarase AgaB gene from the genomic DNA of bacteria in the genus Zobellia was inserted to the 5′ end of a forward primer (SEQ ID NO 21) and the NotI recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 22). Then, PCR was conducted using the synthesized primers. The PCR reaction was conducted at 95° C. for 5 minutes, followed by 30 cycles of 95° C. for 1 minute, 52° C. for 1 minute and 72° C. for 2 minutes, finally at 72° C. for 5 minutes. As a result, a 211-bp PCR band containing the dockerin moiety of the endo-β-1,4-glucanase B gene (SEQ ID NO 23) was observed (result not shown).
C. Construction of Enzyme Complex (β Agarase-Dockerin) Expression Vector
The gene amplification product of the β agarase AgaB gene and the dockerin domain of the cellulase obtained above was subjected to electrophoresis on 0.8% agarose gel. The DNA fragments on the agarose gel were recovered using a gel extraction kit (GeneAll).
Then, overlap PCR was conducted using the recovered DNA fragments in order to link the β agarase AgaB gene with the dockerin domain of cellulase. The overlap PCR reaction was conducted at 94° C. for 2 minutes, followed by 10 cycles of 94° C. for 30 seconds, 52° C. for 25 minutes and 72° C. for 5 minutes, finally at 72° C. for 5 minutes. From the recovered two DNA fragments, primers were designed and synthesized such that the SacI recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 24) and the NotI recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 25). After conducting PCR at 95° C. for 5 minutes, followed by 30 cycles of 95° C. for 1 minute, 52° C. for 1 minute and 72° C. for 2 minutes, finally at 72° C. for 5 minutes, a 1225-bp PCR band containing the chimeric β-agarase AgaB gene derived from Zobellia galactanivorans with the dockerin domain of cellulase linked (SEQ ID NO 26) was observed as the PCT product (result not shown).
Then, after cleaving the dockerin-fused chimeric β-agarase AgaB gene and the AgaB Doc gene, E. coli BL21 was transformed by ligating to the E. coli expression vector pET22b(+) with SacI and NotI. Then, the ligated recombinant plasmid DNA was isolated from the transformant. The recombinant vector was named pET22(+) AgaB-Doc, and the E. coli transformant was named BL21/AgaB-Doc.
3.2 Preparation of Enzyme Complex (Fusion of 3,6-Anhydro-L-Galactosidase and Dockerin)
A. Isolation of 3,6-Anhydro-L-Galactosidase Gene
For cloning of the dockerin domain of cellulase for 3,6-anhydro-L-galactosidase with dockerin bound, primers were designed and synthesized such that the EcoRI recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 27) referring to the base sequence of the 3,6-anhydro-L-galactosidase AhgA gene from the genomic DNA of bacteria in the genus Zobellia and a 10-bp sequence at the N-terminal was inserted to the 5′ end of a reverse primer (SEQ ID NO 28) referring to the base sequence of the dockerin moiety of the endo-β-1,4-glucanase B gene derived from Clostridium cellulovorans. Then, PCR was conducted using the synthesized primers. The PCR reaction was conducted at 95° C. for 5 minutes, followed by 30 cycles of 95° C. for 1 minute, 52° C. for 1 minute and 72° C. for 2 minutes, finally at 72° C. for 5 minutes. As a result, a 1224-bp PCR band containing 3,6-anhydro-L-galactosidase (SEQ ID NO 29) was observed (result not shown).
B. Isolation of Dockerin Gene
Referring to the base sequence of the dockerin moiety of the endo-β-1,4-glucanase B gene from the gDNA of Clostridium cellulovorans, primers were designed and synthesized such that a 10-bp sequence at the C-terminal of the 3,6-anhydro-L-galactosidase AhgA gene from the genomic DNA of bacteria in the genus Zobellia was inserted to the 5′ end of a forward primer (SEQ ID NO 30) and the Hind III recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 31). Then, PCR was conducted using the synthesized primers. The PCR reaction was conducted at 95° C. for 5 minutes, followed by 30 cycles of 95° C. for 1 minute, 52° C. for 1 minute and 72° C. for 2 minutes, finally at 72° C. for 5 minutes. As a result, a 211-bp PCR band containing the dockerin moiety of the endo-β-1,4-glucanase B gene (SEQ ID NO 32) was observed.
C. Construction of Enzyme Complex (Galactosidase-Dockerin) Expression Vector
The gene amplification product of the 3,6-anhydro-L-galactosidase AhgA gene and the dockerin domain of cellulase obtained above was subjected to electrophoresis on 0.8% agarose gel, and the DNA fragments on the agarose gel were recovered using a gel extraction kit (GeneAll).
Then, overlap PCR was conducted using the recovered DNA fragments in order to link the 3,6-anhydro-L-galactosidase AhgA gene and the dockerin domain of cellulase. From the recovered two DNA fragments, primers were designed and synthesized such that the EcoR I recognition sequence was inserted to the 5′ end of a forward primer (SEQ ID NO 33) and the HindIII recognition sequence was inserted to the 5′ end of a reverse primer (SEQ ID NO 34). After conducting PCR at 95° C. for 5 minutes, followed by 30 cycles of 95° C. for 1 minute, 52° C. for 1 minute and 72° C. for 2 minutes, finally at 72° C. for 5 minutes, a 1383-bp PCR band containing the chimeric 3,6-anhydro-L-galactosidase AhgA gene (SEQ ID NO 36) derived from Zobeffia galactanivorans with the dockerin domain of cellulase linked (SEQ ID NO 35) was observed (result not shown).
Expression was induced in the BL21/AgaB-Doc and BL21/AhgA-Doc recombinant strains using 1 mM IPTG at 16° C. for 12 hours. After centrifugation, the cells were lysed by sonication and then centrifuged. Proteins were obtained by concentrating the supernatant (Millipore, Amicon 10 kDa cutoff).
Tagatose conversion activity was investigated using agar as a substrate. More specifically, purified agar was degraded using dockerin-agarase (cAgaB), dockerin-3,6-anhydro-L-galactosidase (cAhgA), dockerin-agarase (cAgaB) or dockerin-3,6-anhydro-L-galactosidase (cAhgA), and then tagatose conversion activity was analyzed after adding the dockerin-arabinose isomerase fusion protein (LsAraA).
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Finally, the enzyme complex according to the present disclosure (β-agarase-3,6-anhydro-L-galactosidase-arabinose isomerase) was prepared as follows. The mini scaffold protein, β-agarase, 3,6-anhydro-L-galactosidase and arabinose isomerase were quantitated to the same concentration of 10 nmol and same proportion and then mixed in a binding solution containing 25 mM CaCl2). Then, reaction was conducted at 4° C. for 24 hours for binding between the cohesin module and the dockerin module.
The activity of the complexes consisting of β-agarase-3,6-anhydro-L-galactosidase-arabinose isomerase and mCbpA with various compositions was analyzed using various agar (purified agar and red algae agar) substrates.
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| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2019-0019901 | Feb 2019 | KR | national |
