Literature DB >> 29310855

Identification of (R)-selective ω-aminotransferases by exploring evolutionary sequence space.

Eun-Mi Kim1, Joon Ho Park2, Byung-Gee Kim3, Joo-Hyun Seo4.   

Abstract

Several (R)-selective ω-aminotransferases (R-ωATs) have been reported. The existence of additional R-ωATs having different sequence characteristics from previous ones is highly expected. In addition, it is generally accepted that R-ωATs are variants of aminotransferase group III. Based on these backgrounds, sequences in RefSeq database were scored using family profiles of branched-chain amino acid aminotransferase (BCAT) and d-alanine aminotransferase (DAT) to predict and identify putative R-ωATs. Sequences with two profile analysis scores were plotted on two-dimensional score space. Candidates with relatively similar scores in both BCAT and DAT profiles (i.e., profile analysis score using BCAT profile was similar to profile analysis score using DAT profile) were selected. Experimental results for selected candidates showed that putative R-ωATs from Saccharopolyspora erythraea (R-ωAT_Sery), Bacillus cellulosilyticus (R-ωAT_Bcel), and Bacillus thuringiensis (R-ωAT_Bthu) had R-ωAT activity. Additional experiments revealed that R-ωAT_Sery also possessed DAT activity while R-ωAT_Bcel and R-ωAT_Bthu had BCAT activity. Selecting putative R-ωATs from regions with similar profile analysis scores identified potential R-ωATs. Therefore, R-ωATs could be efficiently identified by using simple family profile analysis and exploring evolutionary sequence space.
Copyright © 2017 Elsevier Inc. All rights reserved.

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Keywords:  (R)-selective ω-aminotransferase; Branched-chain aminotransferase; Broad substrate specificity; Profile analysis; d-alanine aminotransferase

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Year:  2017        PMID: 29310855     DOI: 10.1016/j.enzmictec.2017.12.002

Source DB:  PubMed          Journal:  Enzyme Microb Technol        ISSN: 0141-0229            Impact factor:   3.493


  1 in total

1.  Improving the catalytic thermostability of Bacillus altitudinis W3 ω-transaminase by proline substitutions.

Authors:  Zihao Xie; Lixin Zhai; Di Meng; Qiaopeng Tian; Zhengbing Guan; Yujie Cai; Xiangru Liao
Journal:  3 Biotech       Date:  2020-06-29       Impact factor: 2.406

  1 in total

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