Literature DB >> 28111248

Improving key enzyme activity in phenylpropanoid pathway with a designed biosensor.

Dandan Xiong1, Shikun Lu1, Jieyuan Wu1, Chaoning Liang2, Wei Wang3, Wenzhao Wang4, Jian-Ming Jin5, Shuang-Yan Tang6.   

Abstract

Overexpressing key enzymes of biosynthetic pathways for overproduction of value-added products usually imposes metabolic burdens on cells, which can be circumvented by improving the key enzyme activities. p-Coumarate: CoA ligase (4CL) is a critical enzyme in the phenylpropanoid pathway that synthesizes various natural products. To screen for 4CL with improved activity, a biosensor of resveratrol whose biosynthetic pathway involves 4CL was designed by engineering the TtgR regulatory protein. The biosensor exhibited good specificity and robustness, allowing rapid and sensitive selection of resveratrol hyper-producers. A 4CL variant with improved activity was selected from a 4CL mutagenesis library constructed in the resveratrol biosynthetic pathway in Escherichia coli. This mutant led to increased production of not only resveratrol but also the flavonoid naringenin, when introduced in their corresponding biosynthetic pathways. These findings demonstrate the feasibility of improving key enzyme activities in important biosynthetic pathways with the aid of designed biosensors of pathway products.
Copyright © 2017 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biosensor; High-throughput screening; Phenylpropanoids pathway; Protein engineering; Resveratrol; p-Coumarate:coenzyme A ligase

Mesh:

Substances:

Year:  2017        PMID: 28111248     DOI: 10.1016/j.ymben.2017.01.006

Source DB:  PubMed          Journal:  Metab Eng        ISSN: 1096-7176            Impact factor:   9.783


  22 in total

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