- Research article
- Open Access
Heterologous expression of a tannic acid-inducible laccase3 of Cryphonectria parasitica in Saccharomyces cerevisiae
© Kim et al; licensee BioMed Central Ltd. 2010
- Received: 22 September 2009
- Accepted: 24 February 2010
- Published: 24 February 2010
A tannic acid-inducible and mycoviral-regulated laccase3 (lac3) from the chestnut blight fungus Cryphonectria parasitica has recently been identified, but further characterization was hampered because of the precipitation of protein products by tannic acid supplementation. The present study investigated the heterologous expression of the functional laccase3 using a yeast Saccharomyces cerevisiae.
Laccase activity in the culture broth of transformants measured using a laccase-specific substrate suggested that the lac3 gene was successfully expressed and the corresponding protein product secreted into the culture media. In addition, activity staining and Western blot analysis of a native gel revealed that the enzyme activity co-existed with the protein product specific to anti-laccase3 antibody, confirming that the cloned lac3 gene is responsible for the laccase activity. When transformants were grown on plates containing tannic acid-supplemented media, brown coloration was observed around transformed cells, indicating the oxidation of tannic acid. However, the enzymatic activity was measurable only in the selective ura- media and was negligible in nonselective nutrient-rich culture conditions. This was in part because of the increased plasmid instability in the nonselective media. Moreover, the protein product of lac3 appears to be sensitive to the cultured nonselective nutrient-rich broth, because a rapid decline in enzymatic activity was observed when the cultured broth of ura- media was mixed with that of nonselective nutrient-rich broth. In addition, constitutive expression of the lac3 gene resulted in a reduced cell number of the lac3 transformants compared to that of vector-only transformed control. However, the presence of recombinant vector without lac3 induction did not affect the growth of transformants.
The results suggest that expression of the lac3 gene has an inhibitory effect on the growth of transformed S. cerevisiae and that the controlled expression of lac3 is appropriate for the possible application of recombinant yeast to the treatment of phenolic compounds.
- Tannic Acid
- Laccase Activity
- Plasmid Stability
- Aspartyl Protease
- Lac3 Gene
Laccases are multi-copper-binding phenoloxidases (EC 220.127.116.11) that were first detected in the Japanese lac tree Toxicodendron verniciflua; they are also found in certain other plants as well as many insects and a variety of fungi [1–3]. Laccases are particularly widespread in ligninolytic basidiomycetes, and more than 125 different basidiomeceteous laccase genes have been described . The biological functions of laccase in fungi are diverse, as laccase is implicated in various cellular processes, including delignification [5, 6], sporulation , pigment production [8–10], fruiting body formation , and pathogenesis [11, 12].
Using oxygen as the final electron acceptor, laccases catalyze the oxidation of a number of aromatic substances such as diphenols, methoxy-substituted monophenols, and aromatic amines . Many laccases are characterized by the presence of one type-1, one type-2, and two type-3 copper ions. One electron at a time is removed from the substrate by a type-1 copper ion and is transferred to the type-2/type-3 copper site, where molecular oxygen is reduced to water . Because of their low substrate specificity, industrial applications for laccases include delignification , the purification of colored waste water , textile dye decoloration , beverage and food treatment , the sulfurization and solublization of coal to their use in enzyme-based biosensors , and the transformation and inactivation of toxic environmental pollutants . In addition, recent studies have shown that the substrate specificity of the enzyme can be broadened in the presence of redox mediators . Given the versatility and broad spectrum of substrate specificity, laccases could become among the most important biocatalysts in fungal biotechnology .
At least three different laccases are present in chestnut blight fungus C. parasitica . Among these, laccase3 is of interest because it is induced specifically by the presence of tannic acid but not by other commonly known fungal laccase inducers such as ferulic acid and 2,5-xylidine, which are structurally related to lignin . In addition, given that C. parasitica is a necrotic fungus rather than a wood-decaying fungus, laccase3 is unique to C. parasitica and is predicted to be involved in overcoming tannic acids, an abundant group of phenolic compounds found in the bark of chestnut tree that function as a natural barriers against pathogen infection. The phenolic metabolism in plants is complex and yields a wide array of compounds ranging from flower pigments to the complex phenolics of the plant cell wall lignin. However, the group of phenolics known as tannic acids is clearly distinguished from other plant phenolics in terms of chemical reactivity and biological activity . Tannic acids are water-soluble phenolic compounds with molecular weights between 500 and 3,000 that exhibit distinct properties such as the ability to precipitate alkaloids, gelatin, and other proteins . The characteristic that sets tannic acids apart from all other phenolics is their ability to precipitate proteins. Therefore, having an enzyme capable of degrading tannic acid or that is insensitive to the presence of tannic acid may be useful for various applications of plant tissue materials. Thus, producing laccase3 on an industrial scale may be useful for processing plant materials with high contents of tannic acid.
Because laccases are notoriously difficult to express in nonfungal systems , several fungi, including Saccharomyces cerevisiae [25, 26], Trichoderma reesei , Aspergillus oryzae , Pichia pastoris , Kluyveromyces lactis , A. sojae , and A. niger , were used for the heterologous expression of laccase. Although P. pastoris has been used as a heterologous host for laccase more often than S. cerevisiae in yeast because of its higher production levels, successful expression in S. cerevisiae has been reported . In addition, S. cerevisiae has a long history of application as a GRAS (Generally Recognized As Safe) organism without the integration of expression constructs. Therefore, we report here the heterologous expression of a novel laccase3 using S. cerevisiae and its effects on the transformed S. cerevisiae.
Analysis of transformed S. cerevisiae
From 10 to 20 transformants of S. cerevisiae representing each recombinant plasmid were selected on ura- medium. Colony PCR using the DNA preparations from these putative transformations revealed the presence of amplified 1.8-kb DNA fragment, indicating that the recombinant plasmid was transferred into yeast. In addition, transformation of E. coli using DNA preparations from all selected transformants confirmed the presence of the recombinant plasmid in yeast.
Expression of LAC3 protein using constitutive promoter
Plasmid stability and cell growth of recombinant strains
CFUs of recombinant strains on YEPD and ura- selective media.
917 ± 27 3
892 ± 22
819 ± 16
813 ± 24
302 ± 17
189 ± 6
98 ± 5
100 ± 4
311 ± 14
217 ± 8
103 ± 3
112 ± 4
351 ± 11
218 ± 7
112 ± 5
112 ± 3
Cell growth was also compared between lac3 transformants and a mock transformant. Compared to the mock transformant, which exhibited 917 CFUs on a YEPD plate, lac3 transformants exhibited less than 40% growth. In addition, when cells were grown in ura- selective broth, further reduction in cell growth (≥ 25% of CFUs) was observed compared to that of a mock transformant (892 CFUs; Table 1).
Effect of cultured broth on expressed LAC3
Even though the number of cells harboring the plasmid was significantly reduced during cultivation of the TYEGLAC3-1 transformant in nonselective YEPD media, a large number of cells still contained the plasmid. It was interesting that no laccase activity was detected in the cultured supernatant of YEPD. We therefore examined enzyme stability by measuring enzyme activity followed by mixing the supernatant of ura- selective broth containing laccase activity with the supernatant of cultured YEPD broth. After 24 h of incubation at 25°C, no laccase activity was observed. However, mixtures with fresh YEPD media or reaction buffer showed laccase activity, indicating that expressed laccase activity is sensitive to cultured YEPD media, whereas laccase activity in the ura- selective media is stably maintained.
Expression of LAC3 protein using an inducible GAL1 promoter
CFUs of recombinant strains TYEGALLAC3-6 on induction and non-induction media.
792 ± 28 3
749 ± 11
763 ± 13
711 ± 23
768 ± 15
391 ± 21
690 ± 17
175 ± 15
Laccase catalyzes one-electron oxidation of diverse substrates with the concomitant reduction of molecular oxygen to water by the transfer of four electrons. Laccases are divided into "low-redox potential" and "high-redox potential" laccases depending on the structure and properties of the copper centers . We recently characterized a new laccase, laccase3, which is induced by the presence of tannic acid . Sequence comparison indicates that laccase3 belongs to the "low-redox potential" group, which is more common in fungi with the exception of white-rot fungi . Given that this enzyme is specific to tannic acid and represents a new laccase from necrotic but not wood-decaying fungus, characterizing its biochemical properties is of interest. However, like most other laccases produced by fungi, its expression level is far too low, and the presence of tannic acid appears to be a limiting factor for protein purification because it precipitates the protein. Therefore, the heterologous expression of functional laccase3 is required for a better understanding and application of this enzyme.
Compared to previous studies that used S. cerevisiae as a laccase expression host, the present study showed a relatively high maximum enzyme activity of 41.5 U/L [25, 37, 38]. However, improved laccase production using S. cerevisiae was achieved by direct evolution and expression of the mature form of laccase, which replaced the endogenous prepropeptide with that of the S. cerevisiae α-factor and removed the inhibitory C-terminal extension [25, 32]. Laccase3 from C. parasitica, like some other laccases from ascomycetes, does not have a C-terminal extension and exhibits C-terminal ends with the last four amino acids of Asp-Ser-Gly-Ile, which represent the processing site . Thus, replacing the endogenous laccase signal peptide with the rice amylase1A signal peptide represents the engineered portion of the recombinant laccase3 gene construct in this study, which may be further manipulated to produce economical levels of expression. In addition to conventional laccase activity on a commonly known substrate such as DMOP, yeast-expressed laccase3 showed the characteristic enzyme activity on tannic acid, which was visualized by coloring the tannic acid-supplemented media on which the recombinant strains expressing laccase3 were grown. Therefore, these results potentiate the possible application of the recombinant yeast strain for treating phenolic waste even in the presence of tannic acid. In addition, the plate assay based on the color reaction showed a clear contrast; i.e., recipient cells showed no browning around the colonies, but dark browning around the colonies was observed in transformants. As in the case of the Bavendamm assay, used to measure the phenol oxidase activity, the area of the colored zone appears to correlate with enzyme activity . Therefore, this test can be further applied as a simple screening method for selecting transformants with higher laccase activity.
Selection pressure to maintain the recombinant vector designed to express the laccase constitutively resulted in a growth defect as detected by the reduced number of cells. However, harboring the vector only without the laccase gene or maintaining the recombinant vector designed to induce the laccase expression under non-inducing conditions did not result in any growth defects. In addition, no significant growth defect was observed by expressing other foreign protein products using a similar constitutive promoter [34, 35]. Moreover, growth defects of transformants using an inducible promoter for laccase expression were observed only when transformants were cultured under induction conditions. Therefore, expression of recombinant laccase3 appears to be harmful to the host cell. This is in accordance with most previous studies, in that an inducible instead of a constitutive promoter was used for the successful expression of laccase in yeast. Like other ligninolytic enzymes, laccases are notoriously bad at producing large amounts as recombinant proteins . One of the possible limitations to the mass production of recombinant laccase is the harmful effect on cell growth observed in this study. Therefore, controlled expression of laccase via the application of an inducible promoter is suggested for the large-scale production of recombinant laccase. Further studies examining the effect of laccase expression on the growth of S. cerevisiae will be of interest.
The expressed protein product of laccase3 was labile to the cultured media of nutrient-rich YEPD. The instability of expressed laccase activity could be due in part to the protease activity in cultured media, because pepstatin (for aspartyl protease) was able to preserve some residual laccase activity. The lack of protection using other protease inhibitors such as aprotinin (for serine protease), EDTA (for metallo protease), E-64 (for cystein protease), leupeptin (for serine/cystein protease), and PMSF (for serine protease) suggests that the residual protease activity is due to the presence of an aspartyl protease, which is expressed under some conditions of fermentation . It is of interest to see that the host strain S. cerevisiae 2805 is a mutant at the pep4 gene encoding protease A (an aspartyl protease). Strain lacking protease A accumulate inactive precursors of protease B and carboxypeptidase Y and show reduced activity of a number of other hydrolases, which consequently results in a significant reduction of overall proteolysis [42, 43]. Therefore, another aspartyl protease may contribute in part to the instability of the laccase. However, there may to be additional reasons for the instability of laccase beyond the protection of residual laccase activity by pepstatin. Whether because of protease activity or other unknown reasons, the instability of laccase seems to be specific rather than general, because the same host strain is used for the expression of various proteins, including enzymes, cytokines, and structural proteins [33, 35, 44], without noticeable instability of expressed target proteins. Therefore, along with the controlled expression of laccase in the recombinant strain, culture conditions that minimize the degradation of expressed laccase, such as using defined simple media rather than complex media, could be applied to improve the production of recombinant laccase3 and to further apply recombinant strains to treat phenolic compounds.
Taken together, this study demonstrated the heterolgous expression of a novel tannic acid-inducible laccase3 and described why laccase expression on commercial scale is difficult. In addition, we have suggested a possible method of producing a large amount of recombinant laccase and discussed the potential of the recombinant strain for bioremediation.
Strains and culture conditions
Plasmids were maintained and propagated in Escherichia coli HB101 or DH5α as described in Sambrook et al. . The cDNA encoding laccase3 from Cryphonectria parasitica was obtained from our previous study , and S. cerevisiae 2805 (MATα pep4::HIS3 prb1-δ can1 GAL2 his3-200 ura3-52) was used for heterologous production of lac3 .
S. cerevisiae was maintained in YEPD medium (yeast extract, 10 g/l; peptone, 20 g/l; dextrose, 20 g/l). Uracil-deficient (ura-) selective medium (6.7 g/l yeast nitrogen base without amino acids, 0.03 g/l adenine and tryptophan, 5 g/l casamino acid, 20 g/l dextrose, 20 g/l agar) was used to screen transformants at 30°C. A primary inoculum was prepared from 5 ml uracil selective medium cultured for 24 h, and 1 × 107 cells were transferred to a 300-ml Erlenmeyer flask containing 40 ml of either YEPD broth or ura- selective broth. Expression cultures were grown at 30°C with continuous agitation (200 rpm) for 2 - 3 days, after which culture supernatants were obtained by centrifugation at 3,000 g and were assayed for laccase activity as described previously .
Transformation and selection of S. cerevisiae
The constructed recombinant vectors were introduced into S. cerevisiae 2805 according to the lithium acetate procedure , and the resulting putative transformants were screened on ura- medium. Colony PCR and back-transformation into E. coli using plasmid preparations from putative transformants were performed to confirm the presence of recombinant plasmids in the yeast.
The stability of the introduced plasmids in the yeast was measured as follows. Samples grown in the nonselective YEPD medium were serially diluted with sterile H2O to an expected 200 colony-forming units (CFUs) per plate and plated on ura- selective and nonselective plates. Then the relative number of CFUs was determined.
The laccase activity in the culture filtrate was determined by spectrophotometric assay using 10 mM 2,6-dimethophenol (DMOP) in sodium tartrate buffer at pH 3.4 as substrate . A laccase unit was defined as a 1.0/min A468 increase at 25°C as described previously .
For the activity staining of native gel, native polyacrylamide gel electrophoresis (PAGE) was performed under non-denaturing conditions ; laccase activity was visualized in the gel using DMOP substrate solution.
Tannic acid-supplemented medium was prepared by adding 0.5% (w/v) tannic acid into uracil-deficient selective medium . Then, transformants were grown on the tannic acid-supplemented medium to visualize the laccase activity by coloring the medium.
Protease inhibition assay
To determine the inhibition of laccase activity due to the presence of protease in cultured media, different types of protease inhibitors, including aprotinin, EDTA, E-64 protease inhibitor, leupeptin, pepstatin, and phenylmethylsulphonyl fluoride (PMSF), were preincubated with cultured media for 10 h at 25°C as recommended previously[41, 49]. The preincubated culture medium was then mixed with the culture media containing laccase activity and incubated further for 24 h, after which the residual laccase activity was measured.
Western blot analysis of expressed laccase3
The partial gene constructs containing the domain from residues 231 to 567 were expressed in E. coli as hexahistidine fusion proteins and purified by nickel affinity chromatography according to the manufacturer's directions (Takara). The cDNA encoding the partial laccase3 was amplified by PCR using the primers 5'-GCAGCTCGAG CTCGAGGACAACAGC-3' (forward) and 5'-CCCAAGCTT TTATATGCCCGA-3' (reverse). The primers were modified to incorporate restriction sites (underlined) for XhoI and HindIII, respectively. The truncated lac3 (1014 bp) was inserted into the XhoI and HindIII sites in the expression vectors pColdII DNA (Takara). The resulting recombinant plasmids were transformed into E. coli strain BL21. Induction, purification, and confirmation of recombinant laccase3 using anti-hexahistidine antibody were conducted according to the manufacturer's directions (Takara).
Anti-CpLac3 antibody was obtained by injecting 100 μg purified partial laccase3 into a 6-week-old BALB/c mouse, which was boosted with the same amount of the laccase3 emulsified in incomplete Freund's adjuvant 2 weeks after the initial injection. Polysera were obtained 5 days after the booster injection and Western blot analysis was conducted according to standard procedures .
This work was supported by the Korea Science and Engineering Foundation (KOSEF) grant funded by the Korean government (MOST; R01-2007-000-10369-0) and in part by the KOSEF grant (R11-2008-062-02002-0). J-MK was supported by the grant of Post-doc. Program, Chonbuk National University (2009). We thank the Research Center of Bioactive Materials and the Institute of Molecular Biology and Genetics at Chonbuk National University for kindly providing the facilities for this research.
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