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Enantiomer discrimination in β-phenylalanine degradation by a newly isolated Paraburkholderia strain BS115 and type strain PsJN

机译:新分离的抛物线虫菌株BS115和PsJN型菌株在β-苯丙氨酸降解中的对映体识别

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摘要

Despite their key role in numerous natural compounds, β-amino acids have rarely been studied as substrates for microbial degradation. Fermentation of the newly isolated Paraburkholderia strain BS115 and the type strain P. phytofirmans PsJN with β-phenylalanine (β-PA) as sole nitrogen source revealed (S)-selective transamination of β-PA to the corresponding β-keto acid by both strains, accompanied by substantial formation of acetophenone (AP) from spontaneous decarboxylation of the emerging β-keto acid. While the PsJN culture became stationary after entire (S)-β-PA consumption, BS115 showed further growth at a considerably slower rate, consuming (R)-β-PA without generation of AP which points to a different degradation mechanism for this enantiomer. This is the first report on degradation of both enantiomers of any β-amino acid by one single bacterial strain.Electronic supplementary materialThe online version of this article (10.1186/s13568-018-0676-2) contains supplementary material, which is available to authorized users.
机译:尽管它们在众多天然化合物中起关键作用,但很少有人研究将β-氨基酸作为微生物降解的底物。以β-苯丙氨酸(β-PA)为唯一氮源发酵新分离出的抛物线菌菌株BS115和P.phytofirmans型PsJN菌株,揭示了这两种菌株将β-PA选择性(S)选择性转氨为相应的β-酮酸伴随着新出现的β-酮酸的自然脱羧而形成的苯乙酮(AP)。虽然在整个(S)-β-PA消耗后PsJN培养物变得稳定,但BS115却以相当慢的速度进一步生长,消耗了(R)-β-PA而没有生成AP,这表明该对映异构体具有不同的降解机理。这是有关单个细菌菌株降解任何β-氨基酸的两种对映异构体的第一份报告。电子补充材料本文的在线版本(10.1186 / s13568-018-0676-2)包含补充材料,可通过授权获得用户。

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