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Production of the Chiral Compound (R)-3-Hydroxybutyrate by a Genetically Engineered Methylotrophic Bacterium

机译:基因改造的甲基营养细菌生产手性化合物(R)-3-羟基丁酸酯

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摘要

In this study, a methylotrophic bacterium, Methylobacterium rhodesianum MB 126, was used for the production of the chiral compound (R)-3-hydroxybutyrate (R-3HB) from methanol. R-3HB is formed during intracellular degradation of the storage polymer (R)-3-polyhydroxybutyrate (PHB). Since the monomer R-3HB does not accumulate under natural conditions, M. rhodesianum was genetically modified. The gene (hbd) encoding the R-3HB-degrading enzyme, R-3HB dehydrogenase, was inactivated in M. rhodesianum. The resulting hbd mutant still exhibited low growth rates on R-3HB as the sole source of carbon and energy, indicating the presence of alternative pathways for R-3HB utilization. Therefore, transposon mutagenesis was carried out with the hbd mutant, and a double mutant unable to grow on R-3HB was obtained. This mutant was shown to be defective in lipoic acid synthase (LipA), resulting in an incomplete citric acid cycle. Using the hbd lipA mutant, we produced 3.2 to 3.5 mM R-3HB in batch and 27 mM (2,800 mg liter−1) in fed-batch cultures. This was achieved by sequences of cultivation conditions initially favoring growth, then PHB accumulation, and finally PHB degradation.
机译:在这项研究中,一种甲基营养细菌,罗氏甲烷菌MB 126,用于由甲醇生产手性化合物(R)-3-羟基丁酸酯(R-3HB)。 R-3HB是在储存聚合物(R)-3-聚羟基丁酸酯(PHB)的细胞内降解过程中形成的。由于单体R-3HB在自然条件下不会积聚,因此对罗氏沼虾进行了基因修饰。编码R-3HB降解酶R-3HB脱氢酶的基因(hbd)在M. rhodesianum中被灭活。所得的hbd突变体在R-3HB作为唯一的碳和能量来源时仍显示出较低的生长速率,表明存在R-3HB利用的替代途径。因此,用hbd突变体进行了转座子诱变,获得了不能在R-3HB上生长的双重突变体。该突变体显示硫辛酸合酶(LipA)有缺陷,导致柠檬酸循环不完整。使用 hbd lipA 突变体,我们分批生产了3.2至3.5 mM R -3HB,在饲料中生产了27 mM(2,800 mg升 -1 )批次文化。这是通过一系列的培养条件实现的,这些条件最初有利于生长,然后有利于PHB积累,最后有利于PHB降解。

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