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Bioproduction of 4-vinylphenol from corn cob alkaline hydrolyzate in two-phase extractive fermentation using free or immobilized recombinant E. coli expressing pad gene

机译:使用游离或固定化重组大肠杆菌表达垫基因在两阶段萃取发酵中从玉米芯碱水解物中生物生产4-乙烯基苯酚

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摘要

In situ extractive Fermentation was used to produce 4-vinyl derivatives from hydroxycinnamic acids extracted from corn cobs by recombinant Escherichia coli cells expressing Lactobacillus plantarum phenolic acid descarboxylase (PAD) gene. This microorganism mainly produced 4-vinylphenol (4VP) from p-coumaric acid (p-CA). In the first study, we observed that the concentrations of 4VP are higher than 1 g/L which had a negative impact on decarboxylation of p-CA to 4VP by recombinant E. coli cells. Because of this, and in order to improve the downstream process, a two-phase aqueous-organic solvent system was developed. The results of the extractive fermentation indicated that it was possible to use hydrolyzates as aqueous phase to bioproduce 4VP, and recover simultaneously the product in the organic phase containing hexane. The detoxification of pre-treated corn cob alkaline hydrolyzate improved 4VP production up to 1003.5 mg/L after 24 h fermentation (Q_p=41.813 mg/L h). Additionally, preliminary experiments using cells immobilized in calcium alginate showed to be a good system for the biotransform of p-CA to 4VP in extractive fermentation, although the process hindered partially the recovery of 4VP in the organic phase.
机译:原位萃取发酵用于通过表达植物乳杆菌酚酸脱羧酶(PAD)基因的重组大肠杆菌细胞从玉米芯提取的羟基肉桂酸生产4-乙烯基衍生物。该微生物主要从对香豆酸(p-CA)产生4-乙烯基苯酚(4VP)。在第一个研究中,我们观察到4VP的浓度高于1 g / L,这对重组大肠杆菌细胞将p-CA脱羧成4VP产生了负面影响。因此,并且为了改善下游工艺,开发了两相水性有机溶剂体系。提取发酵的结果表明,可以使用水解产物作为水相来生物生产4VP,并同时在含有己烷的有机相中回收产物。预处理的玉米芯碱性水解产物的解毒作用,使24小时发酵后的4VP产量提高至1003.5 mg / L(Q_p = 41.813 mg / L h)。此外,使用固定在藻酸钙中的细胞进行的初步实验显示,对于将p-CA生物转化为提取发酵中的4VP而言,这是一个很好的系统,尽管该过程部分阻碍了有机相中4VP的回收。

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