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首页> 外文期刊>Biotechnology and Bioengineering >A Process for Microbial Hydrocarbon Synthesis: Overproduction of Fatty Acids in Escherichia coli and Catalytic Conversion to Alkanes
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A Process for Microbial Hydrocarbon Synthesis: Overproduction of Fatty Acids in Escherichia coli and Catalytic Conversion to Alkanes

机译:微生物碳氢化合物合成的过程:大肠杆菌中脂肪酸的过量生产和催化转化为烷烃

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The development of renewable alternatives to diesel and jet fuels is highly desirable for the heavy transportation sector, and would offer benefits over the production and use of short-chain alcohols for personal transportation. Here, we report the development of a metabolically engineered strain of Escherichia coli that overproduces medium-chain length fatty acids via three basic modifications: elimination of beta-oxidation, overexpression of the four subunits of acetyl-CoA carboxylase, and expression of a plant acyl acyl carrier protein (ACP) thioesterase from Umbellularia californica (BTE). The expression level of BTE was optimized by comparing fatty acid production from strains harboring BTE on plasmids with four different copy numbers. Expression of BTE from low copy number plasmids resulted in the highest fatty acid production. Up to a seven-fold increase in total fatty acid production was observed in engineered strains over a negative control strain (lacking P-oxidation), with a composition dominated by C-12 and C-14 saturated and unsaturated fatty acids. Next, a strategy for producing undecane via a combination of biotechnology and heterogeneous catalysis is demonstrated. Fatty acids were extracted from a culture of an overproducing strain into an alkane phase and fed to a Pd/C plug flow reactor, where the extracted fatty acids were decarboxylated into saturated alkanes. The result is an enriched alkane stream that can be recycled for continuous extractions. Complete conversion of C-12 fatty acids extracted from culture to alkanes has been demonstrated yielding a concentration of 0.44 g L-1 (culture volume) undecane. Biotechnol. Bioeng. 2010;106:193-202.
机译:对于重型运输行业,非常需要开发柴油和喷气燃料的可再生替代品,这将为个人运输使用短链醇的生产和使用带来好处。在这里,我们报告了通过三个基本修饰过量代谢中等链长度脂肪酸的大肠杆菌的代谢工程菌株的开发:消除β-氧化,乙酰辅酶A羧化酶四个亚基的过表达以及植物酰基的表达加利福尼亚伞形藻(BTE)的酰基载体蛋白(ACP)硫酯酶。通过比较带有四个不同拷贝数的质粒上带有BTE的菌株产生的脂肪酸,可以优化BTE的表达水平。从低拷贝数质粒表达BTE导致最高的脂肪酸产量。在工程菌株中观察到的总脂肪酸产量比阴性对照菌株(缺乏P氧化)高出多达7倍,其组成主要由C-12和C-14饱和和不饱和脂肪酸组成。接下来,展示了通过生物技术和非均相催化相结合生产十一烷的策略。从高产菌株的培养物中提取脂肪酸到烷烃相中,并进料到Pd / C活塞流反应器中,在此将提取的脂肪酸脱羧成饱和烷烃。结果是可以将丰富的烷烃物流再循环以进行连续萃取。已证明将从培养物中提取的C-12脂肪酸完全转化为烷烃,可产生浓度为0.44 g L-1(培养物体积)的十一烷。生物技术。生恩2010; 106:193-202。

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