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通过大肠杆菌高效实验设计和微尺度培养基强化 6-脱氧红霉内酯 B 的生产。

Efficient experimental design and micro-scale medium enhancement of 6-deoxyerythronolide B production through Escherichia coli.

机构信息

Dept. of Chemical and Biological Engineering, Tufts University, Medford, MA 02155, USA.

出版信息

Biotechnol Prog. 2009 Sep-Oct;25(5):1364-71. doi: 10.1002/btpr.250.

Abstract

The recent use of heterologous hosts to produce natural products has shown significant potential, although limitations still exist regarding optimal production titers. In this study, we utilize micro-scale cultures and well-defined screening methods to identify key medium components that influence the heterologous production of the complex polyketide 6-deoxyerythronolide B (6dEB) through E. coli. It was determined that tryptone had a significant effect on 6dEB production and could supplement substrate requirements and improve recombinant protein levels of the essential deoxyerythronolide B synthase (DEBS) which catalyze 6dEB conversion. As a result, the study (1) demonstrates the feasibility of micro-scale cultures to study E. coli 6dEB production and effectively model larger-scale cultures; (2) identifies an enhanced medium which generates over 160 mg L(-1) 6dEB (a 22-fold improvement over current culture media); and (3) provides new insight and understanding related to the heterologous production of 6dEB from E. coli.

摘要

近年来,利用异源宿主生产天然产物显示出了巨大的潜力,尽管在最佳生产滴度方面仍存在一些限制。在这项研究中,我们利用微尺度培养和明确的筛选方法来确定关键的培养基成分,这些成分影响大肠杆菌中复杂聚酮体 6-脱氧赤藓醇 B(6dEB)的异源生产。结果表明,蛋白胨对 6dEB 的生产有显著影响,可以补充底物需求并提高必需的 6-脱氧赤藓醇 B 合酶(DEBS)的重组蛋白水平,该酶催化 6dEB 的转化。因此,该研究(1)证明了微尺度培养在研究大肠杆菌 6dEB 生产中的可行性,并有效地模拟了更大规模的培养;(2)确定了一种增强型培养基,可产生超过 160mg/L 的 6dEB(比当前培养基提高了 22 倍);(3)为大肠杆菌中 6dEB 的异源生产提供了新的见解和理解。

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