scholarly journals H2-driven biotransformation of n-octane to 1-octanol by a recombinant Pseudomonas putida strain co-synthesizing an O2-tolerant hydrogenase and a P450 monooxygenase

2015 ◽  
Vol 51 (90) ◽  
pp. 16173-16175 ◽  
Author(s):  
Thomas H. Lonsdale ◽  
Lars Lauterbach ◽  
Sumire Honda Malca ◽  
Bettina M. Nestl ◽  
Bernhard Hauer ◽  
...  

A bacterial whole-cell system was designed for hydroxylation of n-octane to 1-octanol at the expense of molecular hydrogen and oxygen.

Author(s):  
Yeong-Hoon Han ◽  
Hyun Joong Kim ◽  
Tae-Rim Choi ◽  
Hun-Suk Song ◽  
Sun Mi Lee ◽  
...  

2009 ◽  
Vol 75 (12) ◽  
pp. 4202-4205 ◽  
Author(s):  
Wei Wang ◽  
Feng-Qing Wang ◽  
Dong-Zhi Wei

ABSTRACT A new cytochrome P450 monooxygenase, FcpC, from Streptomyces virginiae IBL-14 has been identified. This enzyme is found to be responsible for the bioconversion of a pyrano-spiro steroid (diosgenone) to a rare nuatigenin-type spiro steroid (isonuatigenone), which is a novel C-25-hydroxylated diosgenone derivative. A whole-cell P450 system was developed for the production of isonuatigenone via the expression of the complete three-component electron transfer chain in an Escherichia coli strain.


2017 ◽  
Vol 12 (3) ◽  
pp. 1600520 ◽  
Author(s):  
Jan M. Klenk ◽  
Bernd A. Nebel ◽  
Joanne L. Porter ◽  
Justyna K. Kulig ◽  
Shaneela A. Hussain ◽  
...  
Keyword(s):  
The Self ◽  

2020 ◽  
Vol 22 (13) ◽  
pp. 4128-4132 ◽  
Author(s):  
Stylianos Grigoriou ◽  
Pierre Kugler ◽  
Evelina Kulcinskaja ◽  
Frederik Walter ◽  
John King ◽  
...  

The development and application of a self-sufficient whole-cell system for transaminase biotransformations is described. The system relies on an engineered strain of Corynebacterium glutamicum that produces smart amine donors.


1992 ◽  
Vol 3 (12) ◽  
pp. 1543-1546 ◽  
Author(s):  
Mark A. Cohen ◽  
Julian S. Parratt ◽  
Nicholas J. Turner

Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 400 ◽  
Author(s):  
Md Ahsan ◽  
Mahesh Patil ◽  
Hyunwoo Jeon ◽  
Sihyong Sung ◽  
Taeowan Chung ◽  
...  

ω-Aminododecanoic acid is considered as one of the potential monomers of Nylon 12, a high-performance member of the bioplastic family. The biosynthesis of ω-aminododecanoic acid from renewable sources is an attractive process in the polymer industry. Here, we constructed three artificial self-sufficient P450s (ArtssP450s) using CYP153A13 from Alcanivorax borkumensis and cytochrome P450 reductase (CPR) domains of natural self-sufficient P450s (CYP102A1, CYP102A5, and 102D1). Among them, artificial self-sufficient P450 (CYP153A13BM3CPR) with CYP102A1 CPR showed the highest catalytically activity for dodecanoic acid (DDA) substrate. This form of ArtssP450 was further co-expressed with ω-TA from Silicobacter pomeroyi and AlkJ from Pseudomonas putida GPo1. This single-cell system was used for the biotransformation of dodecanoic acid (DDA) to ω-aminododecanoic acid (ω-AmDDA), wherein we could successfully biosynthesize 1.48 mM ω-AmDDA from 10 mM DDA substrate in a one-pot reaction. The productivity achieved in the present study was five times higher than that achieved in our previously reported multistep biosynthesis method (0.3 mM).


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