Efficient production of trans-4-hydroxy-L-proline from glucose using a new trans-proline 4-hydroxylase in Escherichia coli

被引:23
作者
Wang, Xing-Chu [1 ,2 ,3 ]
Liu, Jiao [1 ,2 ]
Zhao, Jing [1 ,2 ]
Ni, Xiao-Meng [1 ,2 ]
Zheng, Ping [1 ,2 ]
Guo, Xuan [1 ,2 ]
Sun, Cun-Min [1 ,2 ]
Sun, Ji-Bin [1 ,2 ]
Ma, Yan-He [2 ]
机构
[1] Chinese Acad Sci, Key Lab Syst Microbial Biotechnol, Tianjin 300308, Peoples R China
[2] Chinese Acad Sci, Tianjin Inst Ind Biotechnol, Tianjin 300308, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
trans-Proline; 4-hydroxylase; Genome mining; trans-4-Hydroxy-L-proline; Escherichia coli; Fed-batch fermentation; MICROBIAL ENZYMES; HYDROXYLATION; BIOSYNTHESIS; IDENTIFICATION; CONSTRUCTION; PURIFICATION; EXPRESSION; DISCOVERY;
D O I
10.1016/j.jbiosc.2018.04.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
trans-4-Hydroxy-L-proline (trans-4Hyp) is widely used as a valuable building block for the organic synthesis of many pharmaceuticals such as carbapenem antibiotics. The major limitation for industrial bioproduction of trans-4Hyp is the low titer and productivity by using the existing trans-proline 4-hydroxylases (trans-P4Hs). Herein, three new trans-P4Hs from Alteromonas mediterranea (AlP4H), Micromonospora sp. CNB394 (MiP4H) and Sorangium cellulosum (ScP4H) were discovered through genome mining and enzymatic determination. These trans-P4Hs were introduced into an L-proline-producing chassis cell, and the recombinant strain overexpressing AIP4H produced the highest concentration of trans-4Hyp (3.57 g/L) from glucose in a shake flask. In a fed-batch fermentation with a 5 L bioreactor, the best strain SEcH (pTc-B74A-alp4h) accumulated 45.83 g/L of trans-4Hyp within 36 h, with the highest productivity (1.27 g/L/h) in trans-4Hyp fermentation from glucose, to the best of our knowledge. This study provides a promising hydroxylase candidate for efficient industrial production of trans-4Hyp. (C) 2018, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:470 / 477
页数:8
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