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铜绿假单胞菌突变体和野生型培养物中吩嗪色素的生物合成。

Biosynthesis of phenazine pigments in mutant and wild-type cultures of Pseudomonas aeruginosa.

作者信息

Byng G S, Eustice D C, Jensen R A

出版信息

J Bacteriol. 1979 Jun;138(3):846-52. doi: 10.1128/jb.138.3.846-852.1979.

Abstract

Pigmentation mutants of Pseudomonas aeruginosa, selected by observed visual differences in coloration from the wild-type strain, were examined for altered patterns of phenazine synthesis. Three classes of mutants that were incapable of pyocyanine production were identified. Pigmentation patterns that were found to characterize the various mutant classes implicated precursor-product relationships, and a biochemical scheme covering the terminal reactions of pyocyanine biosynthesis is proposed. Among compounds tested as inhibitors of pigmentation, two effectively inhibited pyocyanine production production while allowing cell growth. p-Aminobenzoate inhibited total pigmentation; i.e., no other phenazine accumulated. m-Aminobenzoate inhibited a presumptive methylation step in pyocyanine biosynthesis, abolishing the formation of pyocyanine and aeruginosin pigments but increasing the yields of phenazine 1-carboxylic acid and oxychlororaphin. D-[2,3,4,5(n)-14C]shikimate was most efficiently incorporated into phenazines in the middle to late exponential phase of growth. Label was incorporated predominantly into pyocyanine in the absence of inhibitors and into phenazine 1-carboxylic acid when the organism was grown in the presence of m-aminobenzoate.

摘要

通过观察与野生型菌株在颜色上的视觉差异而筛选出的铜绿假单胞菌色素沉着突变体,被检测其吩嗪合成模式的改变。鉴定出三类无法产生绿脓菌素的突变体。发现表征不同突变体类别的色素沉着模式涉及前体-产物关系,并提出了一个涵盖绿脓菌素生物合成终末反应的生化方案。在作为色素沉着抑制剂进行测试的化合物中,两种化合物有效地抑制了绿脓菌素的产生,同时允许细胞生长。对氨基苯甲酸抑制总色素沉着;即,没有其他吩嗪积累。间氨基苯甲酸抑制绿脓菌素生物合成中的一个假定甲基化步骤,消除绿脓菌素和绿脓青素色素的形成,但增加吩嗪-1-羧酸和氧氯菌素的产量。D-[2,3,4,5(n)-14C]莽草酸在生长的指数中期到后期最有效地掺入吩嗪中。在没有抑制剂的情况下,标记主要掺入绿脓菌素中,而当生物体在间氨基苯甲酸存在下生长时,标记掺入吩嗪-1-羧酸中。

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