Enhancing the thermostability and activity of uronate dehydrogenase from Agrobacterium tumefaciens LBA4404 by semi-rational engineering

Hui-Hui Su , Fei Peng , Pei Xu , Xiao-Ling Wu , Min-Hua Zong , Ji-Guo Yang , Wen-Yong Lou

Bioresources and Bioprocessing ›› 2019, Vol. 6 ›› Issue (1) : 36

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Bioresources and Bioprocessing ›› 2019, Vol. 6 ›› Issue (1) : 36 DOI: 10.1186/s40643-019-0267-3
Research

Enhancing the thermostability and activity of uronate dehydrogenase from Agrobacterium tumefaciens LBA4404 by semi-rational engineering

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Abstract

Background

Glucaric acid, one of the aldaric acids, has been declared a “top value-added chemical from biomass”, and is especially important in the food and pharmaceutical industries. Biocatalytic production of glucaric acid from glucuronic acid is more environmentally friendly, efficient and economical than chemical synthesis. Uronate dehydrogenases (UDHs) are the key enzymes for the preparation of glucaric acid in this way, but the poor thermostability and low activity of UDH limit its industrial application. Therefore, improving the thermostability and activity of UDH, for example by semi-rational design, is a major research goal.

Results

In the present work, three UDHs were obtained from different Agrobacterium tumefaciens strains. The three UDHs have an approximate molecular weight of 32 kDa and all contain typically conserved UDH motifs. All three UDHs showed optimal activity within a pH range of 6.0–8.5 and at a temperature of 30 °C, but the UDH from A. tumefaciens (At) LBA4404 had a better catalytic efficiency than the other two UDHs (800 vs 600 and 530 s−1 mM−1). To further boost the catalytic performance of the UDH from AtLBA4404, site-directed mutagenesis based on semi-rational design was carried out. An A39P/H99Y/H234K triple mutant showed a 400-fold improvement in half-life at 59 °C, a 5 °C improvement in $ {\text{T}}_{ 5 0}^{ 1 0} $ value and a 2.5-fold improvement in specific activity at 30 °C compared to wild-type UDH.

Conclusions

In this study, we successfully obtained a triple mutant (A39P/H99Y/H234K) with simultaneously enhanced activity and thermostability, which provides a novel alternative for the industrial production of glucaric acid from glucuronic acid.

Keywords

Uronate dehydrogenase / Semi-rational engineering / Biocatalysis / Glucuronic acid / Glucaric acid

Cite this article

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Hui-Hui Su, Fei Peng, Pei Xu, Xiao-Ling Wu, Min-Hua Zong, Ji-Guo Yang, Wen-Yong Lou. Enhancing the thermostability and activity of uronate dehydrogenase from Agrobacterium tumefaciens LBA4404 by semi-rational engineering. Bioresources and Bioprocessing, 2019, 6(1): 36 DOI:10.1186/s40643-019-0267-3

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References

[1]

Aldemita RR, Hodges TK. Agrobacterium tumefaciens mediated transformation of japonica and indica rice varieties. Planta, 1996, 199: 612-617.

[2]

Alponti JS, Fonseca-Maldonado R, Ward RJ. Thermostabilization of Bacillus subtilis gh11 xylanase by surface charge engineering. Int J Biol Macromol, 2016, 87: 522-528.

[3]

Arnold FH, Wintrode PL, Miyazaki K, Gershenson A. How enzymes adapt: lessons from directed evolution. Trends Biochem Sci, 2001, 26: 100-106.

[4]

Bespalov VG, Aleksandrov VA. Anticarcinogenic effect of potassium salts of glucaric and glucuronic acid in induced models of cervical and esophageal tumors. Vopr Onkol, 2012, 58: 537-540.

[5]

Biasini M, Bienert S, Waterhouse A, Arnold K, Studer G, Schmidt T, Kiefer F, Cassarino TG, Bertoni M, Bordoli L, Schwede T. Swiss-model: modelling protein tertiary and quaternary structure using evolutionary information. Nucleic Acids Res, 2014, 42: W252-W258.

[6]

Blair JA, Rauh D, Kung, Yun CH, Fan QW, Rode H, Zhang C, Eck MJ, Weiss WA, Shokat KM. Structure-guided development of affinity probes for tyrosine kinases using chemical genetics. Nat Chem Biol, 2007, 3: 229-238.

[7]

Burley SK, Petsko GA. Aromatic-aromatic interaction: a mechanism of protein structure stabilization. Science, 1985, 229: 23-28.

[8]

Deng Z, Yang H, Shin HD, Li J, Liu L. Structure-based rational design and introduction of arginines on the surface of an alkaline α-amylase fromalkalimonas amylolyticafor improved thermostability. Appl Microbiol Biotechnol, 2014, 98: 8937-8945.

[9]

Dwivedi C, Heck WJ, Downie AA, Larroya S, Webb TE. Effect of calcium glucarate on β-glucuronidase activity and glucarate content of certain vegetables and fruits. Biochem Med Metab Biol, 1990, 43: 83-92.

[10]

Eijsink VGH, Bjork A, Gaseidnes S, Sirevag R, Synstad B, Burg BVD, Vriend G. Rational engineering of enzyme stability. J Biotechnol, 2004, 113: 105-120.

[11]

Etzl S, Lindner R, Nelson MD, Winkler A. Structure-guided design and functional characterization of an artificial red light-regulated guanylate/adenylate cyclase for optogenetic applications. J Biol Chem, 2018, 293: 9078-9089.

[12]

Giver L, Gershenson A, Feskgard P, Arnold FH. Directed evolution of a thermostable esterase. Proc Natl Acad Sci USA, 1998, 95: 12809-12813.

[13]

Hoffmann F, Sotriffer C, Evers A, Xiong GM, Maser. Understanding oligomerization in 3alpha-hydroxysteroid dehydrogenase/carbonyl reductase from Comamonas testosteroni: an in silico approach and evidence for an active protein. J Biotechnol, 2007, 129: 131-139.

[14]

Istomin A, Gromiha MO, Jacobs D, Livesay D. New insight into long-range nonadditivity within protein double-mutant cycles. Proteins, 2010, 70: 915-924.

[15]

Katoh R, Nagata S, Misono H. Cloning and sequencing of the leucine dehydrogenase gene form Bacillus sphaericus IFO3525 and importance of the C-terminal region for the enzyme activity. J Mol Catal B Enzym, 2003, 23: 239-247.

[16]

Kokkinidis M, Glykos NM, Fadouloglou VE. Protein flexibility and enzymatic catalysis. Adv Protein Chem Struct Biol, 2012, 87: 181-218.

[17]

Komari T, Hiei Y, Saito Y, Murai N, Kumashiro T. Vectors carrying two separate T-DNAs for co-transformation of higher plants mediated by Agrobacterium tumefaciens and segregation of transformants free from selection markers. Plant J, 2010, 10: 165-174.

[18]

Kruger N. The bradford method for protein quantitation. Methods Mol Biol, 1988, 32: 9-15.

[19]

Li YX, Xue YM, Cao ZG, Zhou T, Alnadari F. Characterization of a uronate dehydrogenase from Thermobispora bispora for production of glucaric acid from hemicellulose substrate. World J Microbiol Biotechnol, 2018, 34: 102.

[20]

Moon TS, Yoon SH, Lanza AM, Roy-mayhew JD, Prather KL. Enhancing production of glucaric acid from a synthetic pathway in recombinant escherichia coli. Appl Environ Microbiol, 2009, 75: 589-595.

[21]

Morton DW, Kiely DE. Evaluation of the film and adhesive properties of some block copolymer polyhydroxypolyamides from esterified aldaric acids and diamines. J Appl Polym Sci, 2000, 77: 3085-3092.

[22]

Nguyen V, Wilson C, Hoemberger M, Stiller JB, Agafonov RV, Kutter S, Theobald DL, Kern D. Evolutionary drivers of thermoadaptation in enzyme catalysis. Science, 2017, 355: 289-294.

[23]

Parkkinen T, Boer H, Janis J, Andberg M, Penttila M, Koivula A, Rouvinen J. Crystal structure of uronate dehydrogenase from agrobacterium tumefaciens. J Biol Chem, 2011, 286(31): 27294-27300.

[24]

Pick A, Schmid J, Sieber V. Characterization of uronate dehydrogenases catalysing the initial step in an oxidative pathway. Microb Biotechnol, 2015, 8: 633-643.

[25]

Reetz MT. The importance of additive and non-additive mutational effects in protein engineering. Angew Chem Int Ed, 2013, 52: 2658-2666.

[26]

Reetz MT, Soni P, Acevedo JP, Sanchis J. Creation of an amino acid network of structurally coupled residues in the directed evolution of a thermostable enzyme. Angew Chem Int Ed, 2010, 48: 8268-8272.

[27]

Roth T, Beer B, André P, Sieber V. Thermostabilization of the uronate dehydrogenase from Agrobacterium tumefaciens by semi-rational design. AMB Express, 2017, 7: 103.

[28]

Ruller R, Deliberto L, Ward R. Thermostable variants of the recombinant xylanase A from Bacillus subtilis produced by directed evolution show reduced heat capacity changes. Proteins, 2010, 70: 1280-1293.

[29]

Samuel S, Jörg C, Volker S. Structure-guided engineering of α-keto acid decarboxylase for the production of higher alcohols at elevated temperature. Chemsuschem, 2018, 11: 3335-3344.

[30]

Stellwagen E, Wilgus H. Relationship of protein thermostability to accessible surface area. Nat, 1978, 275: 342-343.

[31]

Sutiono S, Carsten J, Sieber V. Structure-Guided Engineering of α-Keto Acid Decarboxylase for the production of higher alcohols at elevated temperature. ChemSusChem, 2018, 11(8): 3335-3344.

[32]

Tanner JJ, Hecht RM, Krause KL. Determinants of enzyme thermostability observed in the molecular structure of thermusaquaticusd-glyceraldehyde-3-phosphate dehydrogenase at 2.5 Å resolution. Biochem, 1996, 35: 2597-2609.

[33]

Thomas JL, Mason JI, Brandt S, Spencer BR, Norris W. Structure/function relationships responsible for the kinetic differences between human type 1 and type 2 3 beta-hydroxysteroid dehydrogenase and for the catalysis of the type 1 activity. J Biol Chem, 2002, 277: 42795-42801.

[34]

Wagner G, Hollmann S. Uronic acid dehydrogenase from Pseudomonas syringae. J Biochem, 1976, 61: 589-596.

[35]

Wagschal K, Jordan DB, Lee CC, Younger A, Braker JD, Chan VJ. Biochemical characterization of uronate dehydrogenases from three Pseudomonads, Chromohalobacter salixigens, and Polaromonas naphthalenivorans. Enzyme Microb Technol, 2015, 69: 62-68.

[36]

Walaszek Z. Potential use of d-glucaric acid derivatives in cancer prevention. Cancer Lett, 1990, 54(1–2): 1-8.

[37]

Werpy TA, Holladay JE. White JF (2004) Top value added chemicals from biomass: I. Results of screening for potential candidates from sugars and synthesis gas. Synthetic Fuels, 2004, 1: 263-275.

[38]

Wijma HJ, Floor RJ, Janssen DB. Structure- and sequence-analysis inspired engineering of proteins for enhanced thermostability. Curr Opin Struct Biol, 2013, 23: 588-594.

[39]

Wintrode PL, Zhang D, Vaidehi N, Arnold FH, Iii WAG. Protein dynamics in a family of laboratory evolved thermophilic enzymes. J Mol Biol, 2003, 327: 745-757.

[40]

Wu ZY, Deng WF, Tong YP, Liao Q, Xin DM, Yu HS, Feng J, Tang LX. Exploring the thermostable properties of halohydrin dehalogenase from Agrobacterium radiobacter AD1 by a combinatorial directed evolution strategy. Appl Microbiol Biotechnol, 2017, 101: 3201-3211.

[41]

Yang DF, Wei YT, Huang RB. Computer-aided design of the stability of pyruvate formate-lyase from Escherichia coli by site-directed mutagenesis. Biosci Biotechnol Biochem, 2007, 71: 746-753.

[42]

Yoon SH, Moon TS, Iranpour P, Lanza AM, Prather KJ. Cloning and characterization of uronate dehydrogenases from two Pseudomonads and Agrobacterium tumefaciens strain c58. J Biotechnol, 2009, 191: 1565-1573.

[43]

Zajic JE. Hexuronic dehydrogenase of Agrobacterium tumefaciens. J Bacteriol, 1959, 78: 734-735.

[44]

Zhang XF, Yang GY, Zhang Y, Xie Y, Withers SG, Feng Y. A general and efficient strategy for generating the stable enzymes. Sci Rep, 2016, 6: 33797.

[45]

Zhou W, Huang R, Zhu Z, Zhang Y. Coevolution of both thermostability and activity of polyphosphate glucokinase from Thermobifida fusca YX. Appl Environ Microbiol, 2018, 84: e01224.

[46]

Zhu QQ, He WH, Kong XD, Fan LQ, Zhao J, Li SX, Xu JH. Heterologous overexpression of vigna radiata, epoxide hydrolase in escherichia coli, and its catalytic performance in enantioconvergent hydrolysis of p-nitrostyrene oxide into (r)-p-nitrophenyl glycol. Appl Microbiol Biotechnol, 2014, 98: 207-218.

[47]

Zółtaszek R, Hanausek M, Kiliańska ZM, Walaszek Z. The biological role of d-glucaric acid and its derivatives: potential use in medicine. Postepy Hig Dosw, 2008, 62: 451-642.

Funding

National Natural Science Foundation of China(21676104)

National Natural Science Foundation of China(21878105)

Gulf Research Program(2018YFC1603400)

National Basic Research Program of China (973 Program) (CN)(2018YFC1602100)

the Science and Technology Program of Guangzhou(201904010360)

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