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Bioconversion of Cinnamic Acid to Acetophenone by a Pseudomonad: Microbial Production of a Natural Flavor Compound

机译:肉桂酸将肉桂酸生物转化为苯乙酮:天然香料化合物的微生物生产

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摘要

A mutant derivative of a novel pseudomonad isolated from the soil accumulated acetophenone when supplied with cinnamic acid. The microorganism has been identified as an unclassified Pseudomonas sp., similar to Pseudomonas acidovorans. Mass spectrum analysis of the product acetophenone derived from catabolism of cinnamic acid in the presence of 18O2 or H218O supported the conclusion that cinnamic acid degradation is initiated by addition of water to the double bond of the side chain, followed by dehydrogenation to generate 3-keto-3-phenylpropionic acid. The intermediate 3-keto-3-phenylpropionic acid is accumulated in cultures of the mutant during active cinnamic acid catabolism. However, this intermediate is unstable so a portion of it spontaneously decarboxylates to form acetophenone. Neither 3-keto-3-phenylpropionic acid nor acetophenone is a precedented intermediate in cinnamic acid degradation. Isolation of the novel strain and mutant provide the rudiments for a process to produce natural acetophenone by biotransformation of natural cinnamic acid.
机译:当提供肉桂酸时,从土壤中分离出的新型假单胞菌的突变体衍生物会积聚苯乙酮。该微生物已被鉴定为未分类的假单胞菌,类似于酸假单胞菌。在 18 O2或H2 18 O存在下肉桂酸分解代谢产物苯乙酮的质谱分析支持以下结论:肉桂酸降解是通过加水引发的在侧链的双键上键合,然后脱氢生成3-酮-3-苯基丙酸。中间体3-酮-3-苯基丙酸在肉桂酸分解代谢过程中积累在突变体的培养物中。然而,该中间体不稳定,因此其一部分自发地脱羧形成苯乙酮。 3-肉桂基-3-苯基丙酸和苯乙酮都不是肉桂酸降解中的先导中间体。新菌株和突变体的分离为通过天然肉桂酸的生物转化生产天然苯乙酮的过程提供了基础。

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