Literature DB >> 9807838

Novel biosynthetic approaches to the production of unnatural amino acids using transaminases.

P P Taylor1, D P Pantaleone, R F Senkpeil, I G Fotheringham.   

Abstract

Transaminase enzymes are being increasingly applied to the large-scale synthesis of unnatural and nonproteinogenic amino acids. Typically displaying relaxed substrate specificity, rapid reaction rates and lacking the need for cofactor regeneration, they possess many characteristics that make them desirable as effective biocatalysts. By judiciously combining the transaminase reaction with additional enzymatic steps, this approach can be used very efficiently to prepare a broad range of D- and L-amino acids.

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Year:  1998        PMID: 9807838     DOI: 10.1016/s0167-7799(98)01240-2

Source DB:  PubMed          Journal:  Trends Biotechnol        ISSN: 0167-7799            Impact factor:   19.536


  30 in total

1.  Expanding metabolism for total biosynthesis of the nonnatural amino acid L-homoalanine.

Authors:  Kechun Zhang; Han Li; Kwang Myung Cho; James C Liao
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-23       Impact factor: 11.205

2.  Cloning and characterization of a novel beta-transaminase from Mesorhizobium sp. strain LUK: a new biocatalyst for the synthesis of enantiomerically pure beta-amino acids.

Authors:  Juhan Kim; Dohyun Kyung; Hyungdon Yun; Byung-Kwan Cho; Joo-Hyun Seo; Minho Cha; Byung-Gee Kim
Journal:  Appl Environ Microbiol       Date:  2007-01-26       Impact factor: 4.792

3.  Purification, crystallization and preliminary X-ray crystallographic analysis of branched-chain aminotransferase from Deinococcus radiodurans.

Authors:  Chung-Der Chen; Tien-Feng Huang; Chih-Hao Lin; Hong-Hsiang Guan; Yin-Cheng Hsieh; Yi-Hung Lin; Yen-Chieh Huang; Ming-Yih Liu; Wen-Chang Chang; Chun-Jung Chen
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-05-05

4.  ω-Transaminase from Ochrobactrum anthropi is devoid of substrate and product inhibitions.

Authors:  Eul-Soo Park; Jong-Shik Shin
Journal:  Appl Environ Microbiol       Date:  2013-04-12       Impact factor: 4.792

5.  Dihydrophenylalanine: a prephenate-derived Photorhabdus luminescens antibiotic and intermediate in dihydrostilbene biosynthesis.

Authors:  Jason M Crawford; Sarah A Mahlstedt; Steven J Malcolmson; Jon Clardy; Christopher T Walsh
Journal:  Chem Biol       Date:  2011-09-23

6.  Use of enrichment culture for directed evolution of the Vibrio fluvialis JS17 omega-transaminase, which is resistant to product inhibition by aliphatic ketones.

Authors:  Hyungdon Yun; Bum-Yeol Hwang; Jae-Hun Lee; Byung-Gee Kim
Journal:  Appl Environ Microbiol       Date:  2005-08       Impact factor: 4.792

7.  Structural determinants of the β-selectivity of a bacterial aminotransferase.

Authors:  Gjalt G Wybenga; Ciprian G Crismaru; Dick B Janssen; Bauke W Dijkstra
Journal:  J Biol Chem       Date:  2012-06-28       Impact factor: 5.157

8.  L-selective amidase with extremely broad substrate specificity from Ochrobactrum anthropi NCIMB 40321.

Authors:  Theo Sonke; Sandra Ernste; Renate F Tandler; Bernard Kaptein; Wilco P H Peeters; Friso B J van Assema; Marcel G Wubbolts; Hans E Schoemaker
Journal:  Appl Environ Microbiol       Date:  2005-12       Impact factor: 4.792

9.  Crystal structures of complexes of the branched-chain aminotransferase from Deinococcus radiodurans with α-ketoisocaproate and L-glutamate suggest the radiation resistance of this enzyme for catalysis.

Authors:  Chung-De Chen; Chih-Hao Lin; Phimonphan Chuankhayan; Yen-Chieh Huang; Yin-Cheng Hsieh; Tien-Feng Huang; Hong-Hsiang Guan; Ming-Yih Liu; Wen-Chang Chang; Chun-Jung Chen
Journal:  J Bacteriol       Date:  2012-09-14       Impact factor: 3.490

10.  Active-Site Engineering of ω-Transaminase for Production of Unnatural Amino Acids Carrying a Side Chain Bulkier than an Ethyl Substituent.

Authors:  Sang-Woo Han; Eul-Soo Park; Joo-Young Dong; Jong-Shik Shin
Journal:  Appl Environ Microbiol       Date:  2015-07-31       Impact factor: 4.792

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