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2015

1. Yin JG, Xu GC, Zheng GW*, Xu JH* (2015). Cloning and characterization of an enantioselective l-menthyl benzoate hydrolase from Acinetobacter sp. ECU2040. Appl Biochem Biotechnol, DOI 10.1007/s12010-015-1632-0.

http://link.springer.com/article/10.1007/s12010-015-1632-0

2. Huang L, Xu JH, Yu HL* (2015). Significantly improved thermostability of a reductase CgKR1 from Candida glabata with a key mutation at Asp 138 for enhancing bioreduction of aromatic α-keto esters. Journal of Biotechnology, 203: 54-61.

http://www.sciencedirect.com/science/article/pii/S0168165615001005

 

3. Zhang YJ, Zhang WX, Zheng GW*, Xu JH* (2015). Identification of an ε-keto ester reductase for the efficient synthesis of an (R)-α-Lipoic acid precursor. Advanced Synthesis & Catalysis, 357: 1697-1702.

http://onlinelibrary.wiley.com/doi/10.1002/adsc.201500001/abstract

 

4. Li H, Luan ZJ, Zheng GW*, Xu JH* (2015). Efficient synthesis of chiral indolines using an imine reductase from Paenibacillus lactis. Advanced Synthesis & Catalysis, 357: 1692-1696.

http://onlinelibrary.wiley.com/doi/10.1002/adsc.201500160/abstract

 

5. Chen Q, Luan ZJ, Cheng X*, Xu JH* (2015). Molecular dynamics investigation of the substrate binding mechanism in caroxylesterase. Biochemistry, 54: 1841-1848.

http://pubs.acs.org/doi/abs/10.1021/bi5015612

6. Luan ZJ, Li FL, Dou S, Chen Q, Kong XD, Zhou JH, Yu HL*, Xu JH* (2015). Substrate channel evolution of esterase for the synthesis of cilastatin. Catal. Sci. Technol., 5: 2622-2629.

http://pubs.rsc.org/en/Content/ArticleLanding/2015/CY/C5CY00085H

 

7. Luan ZJ, Yin YC, Li AT, Yu HL*, Xu JH* (2015). Monoterpene hydroxylation with an artificial self-sufficient P450 utilizing a P450SMO reductase domain for the electron transfer. J Mol Catal B: Enzym, 116: 78-82.

http://www.sciencedirect.com/science/article/pii/S1381117715000478

 

8. Zhang ZJ, Yu HL, Imanaka T, Xu JH* (2015). Efficient production of (R)-(-)-mandelic acid by isopropanol-permeabilized recombinant E. coli cells expressing Alcaligenes sp. Nitrilase. Biochemical Engineering Journal, 95: 71-77.

http://www.sciencedirect.com/science/article/pii/S1369703X14003581

9. Zheng MM, Wang RF, Li CX, Xu JH* (2015). Two-step enzymatic synthesis of ursodeoxycholic acid with a new 7β-hydroxysteroid dehydrogenase from Ruminococcus torques. Process Biochemistry, 50: 598-604.

http://www.sciencedirect.com/science/article/pii/S1359511315000112

 

10. Wang RF, Zheng MM, Cao YD, Li H, Li CX, Xu JH*, Wang ZT* (2015). Biotransformation of vina-ginsenoside R7 to rare notoginsenoside ST-4 using a new recombinant glycoside hydrolase from Herpetosiphon aurantiacus. Appl. Microbiol. Biotechnol., 99: 3433-3442.

http://link.springer.com/article/10.1007%2Fs00253-015-6446-z

11. Xu GC, Yu HL*, Shang YP, Xu JH* (2015). Enantioselective bioreductve preparation of chiral halohydrins employing two newly identified stereocomplementary reductases. RSC Advances, 5: 22703-22711. 

http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/C4RA16779A

 

12. Fan CW, Ma BD, Xu GC, Bai YP, Zhang J, Xu JH* (2015). A novel D-mandelate dehydrogenase used in three-enzyme cascade reaction for highly efficient synthesis of non-natural chiral amino acids. Journal of Biotechnology, 195: 67-71. 

http://www.sciencedirect.com/science/article/pii/S0168165614009341

 

13. Liu JY, Bian HP, Tang Y, Bai YP, Xu JH* (2015). Double substituted variant of Bacillus amyloliquefaciens esterase with enhanced enantioselectivity and high activity towards 1-(3’,4’-methylenedioxyphenyl)ethyl acetate. Appl. Microbiol. Biotechnol., 99: 1701-1708.

http://link.springer.com/article/10.1007%2Fs00253-014-5992-0

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