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Optimization of naringenin and p‐coumaric acid hydroxylation using the native E. coli hydroxylase complex,HpaBC
Authors:J. Andrew Jones  Shannon M. Collins  Victoria R. Vernacchio  Daniel M. Lachance  Mattheos A. G. Koffas
Affiliation:1. Dept. of Chemical and Biological Engineering, Rensselaer Polytechnic Inst., Troy, NY;2. Dept. of Biological Sciences, Rensselaer Polytechnic Inst., Troy, NY
Abstract:Flavonoids are a growing class of bioactive natural products with distinct and interesting bioactivity both in vitro and in vivo. The extraction of flavonoids from plant sources is limited by their low natural abundance and commonly results in a mixture of products that are difficult to separate. However, due to recent advances, the microbial production of plant natural products has developed as a promising alternative for flavonoid production. Through optimization of media, induction temperature, induction point, and substrate delay time, we demonstrate the highest conversion of naringenin to eriodictyol (62.7 ± 2.7 mg/L) to date, using the native E. coli hydroxylase complex, HpaBC. We also show the first evidence of in vivo HpaBC activity towards the monohydroxylated flavan‐3‐ol afzelechin with catechin product titers of 34.7 ± 1.5 mg/L. This work confirms the wide applicability of HpaBC towards realizing efficient de novo production of various orthohydroxylated flavonoids and flavonoid derived products in E. coli. © 2015 American Institute of Chemical Engineers Biotechnol. Prog., 32:21–25, 2016
Keywords:hydroxylation  non‐P450 hydroxylase  pathway optimization  flavonoids  catechin
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