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首页> 外文期刊>Advances in Microbiology >Evaluation of Carbon and Electron Flow in Lactobacillus brevis as a Potential Host for Heterologous 1-Butanol Biosynthesis
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Evaluation of Carbon and Electron Flow in Lactobacillus brevis as a Potential Host for Heterologous 1-Butanol Biosynthesis

机译:短乳杆菌作为异源1-丁醇生物合成的潜在宿主的碳和电子流的评估

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Heterofermentative lactic acid bacterium Lactobacillus brevis may be considered as a promising host for heterologous butanol synthesis because of tolerance to butanol and ability to ferment pentose and hexose sugars from wood hydrolysates that are cheap and renewable carbohydrate source. Carbon and electron flow was evaluated in two L. brevis strains in order to assess metabolic potential of these bacteria for heterologous butanol synthesis. Conditions required for generation of acetyl-CoA and NADH which are necessary for butanol biosynthesis have been determined. Key enzymes controlling direction of metabolic fluxes in L. brevis in various redox conditions were defined. In anaerobic glucose fermentation, the carbon flow through acetyl-CoA is regulated by aldehyde dehydrogenase ALDH possessing low affinity to NADH and activity (KmNADH= 200 μM, Vmax= 0.03 U/mg of total cell protein). Aerobically, the NADH-oxidase NOX (KmNADH= 25 μM, Vmax = 1.7 U/mg) efficiently competes with ALDH for NADH that results in formation of acetate instead of acetyl-CoA. In general, external electron acceptors (oxygen, fructose) and pentoses decrease NADH availability for native ethanol and recombinant butanol enzymes and therefore reduce carbon flux through acetyl-CoA. Pyruvate metabolism was studied in order to reveal redirection possibilities of competitive carbon fluxes towards butanol synthesis. The study provides a basis for the rational development of L. brevis strains producing butanol from wood hydrolysate.
机译:由于对丁醇的耐受性和能够从廉价且可再生的碳水化合物来源的木材水解物中发酵戊糖和己糖的能力,异发酵性乳酸细菌短乳杆菌可被认为是异丁醇合成的有希望的宿主。为了评估这些细菌在异丁醇合成中的代谢潜力,在两个短乳杆菌中评估了碳和电子的流量。已经确定了丁醇生物合成所必需的产生乙酰辅酶A和NADH所需的条件。定义了在各种氧化还原条件下控制短短乳杆菌代谢通量方向的关键酶。在厌氧葡萄糖发酵中,通过乙酰辅酶A的碳流量受到对NADH亲和力低(KmNADH = 200μM,Vmax = 0.03 U / mg总细胞蛋白)的醛脱氢酶ALDH的调节。有氧运动中,NADH氧化酶NOX(KmNADH = 25μM,Vmax = 1.7 U / mg)与ALDH有效竞争NADH,导致形成乙酸盐而不是乙酰辅酶A。通常,外部电子受体(氧气,果糖)和戊糖会降低天然乙醇和重组丁醇酶的NADH利用率,因此会降低通过乙酰辅酶A的碳通量。对丙酮酸的代谢进行了研究,以揭示竞争性碳通量向丁醇合成的重定向可能性。该研究为合理开发由木材水解产物生产丁醇的短乳杆菌菌株提供了基础。

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