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硫胺素诱导灵菌红素单吡咯部分的形成。

Thiamine-induced formation of the monopyrrole moiety of prodigiosin.

作者信息

Goldschmidt M C, Williams R P

出版信息

J Bacteriol. 1968 Sep;96(3):609-16. doi: 10.1128/jb.96.3.609-616.1968.

Abstract

Thiamine stimulates the production of a red pigment, which is chromatographically and spectrophotometrically identical to prodigiosin, by growing cultures of Serratia marcescens mutant 9-3-3. This mutant is blocked in the formation of 2-methyl-3-amylpyrrole (MAP), the monopyrrole moiety of prodigiosin, but accumulates 4-methoxy-2,2,'-bipyrrole-5-carboxaldehyde (MBC) and can couple this compound with MAP to form prodigiosin. Addition of thiamine caused production of MAP, and as little as 0.02 mg of thiamine per ml in a peptone-glycerol medium stimulated production of measurable amounts of prodigiosin. Phosphate salts and another type of peptone decreased the thiamine-induced formation of prodigiosin; yeast extract and glycerol enhanced the formation of this substance. Thiamine also enhanced production of prodigiosin by wild-type strain Nima of S. marcescens. The thiamine antagonists, oxythiamine and pyrithiamine, inhibited thiamine-induced production of MAP and of prodigiosin by the mutant strain 9-3-3, formation of prodigiosin by the wild-type strain Nima, and production of MAP by another mutant, strain WF. The pyrimidine moiety of thiamine was only 10% as effective as the vitamin; the thiazole moiety, only 4%; and the two moieties together, 25%. Various other vitamins tested did not stimulate formation of prodigiosin by strain 9-3-3. Thiamine did not stimulate production of prodigiosin by a single-step mutant that showed the same phenotypic block in prodigiosin biosynthesis as strain 9-3-3. This is not surprising since strain 9-3-3 originated as a result of two mutational events. One event may involve thiamine directly, and the other may involve the biosynthesis of MAP. Thiamine is probably involved in the regulation of the biosynthesis of MAP, because the vitamin or inhibitory antagonists must be added during the early phases of growth in order to be effective.

摘要

硫胺素可刺激粘质沙雷氏菌突变体9-3-3的培养物生成一种红色色素,该色素在色谱和分光光度法上与灵菌红素相同。此突变体在灵菌红素的单吡咯部分2-甲基-3-戊基吡咯(MAP)的形成过程中受阻,但会积累4-甲氧基-2,2'-联吡咯-5-甲醛(MBC),并能将该化合物与MAP偶联形成灵菌红素。添加硫胺素会导致MAP的产生,在蛋白胨-甘油培养基中每毫升添加低至0.02毫克硫胺素就能刺激产生可测量量的灵菌红素。磷酸盐和另一种蛋白胨会降低硫胺素诱导的灵菌红素形成;酵母提取物和甘油则会增强该物质的形成。硫胺素还能增强粘质沙雷氏菌野生型菌株尼玛的灵菌红素产生。硫胺素拮抗剂氧硫胺素和吡硫胺素可抑制突变体菌株9-3-3由硫胺素诱导的MAP和灵菌红素产生、野生型菌株尼玛的灵菌红素形成以及另一个突变体菌株WF的MAP产生。硫胺素的嘧啶部分的效果仅为该维生素的10%;噻唑部分仅为4%;两者合起来为25%。所测试的其他各种维生素均未刺激菌株9-3-3形成灵菌红素。硫胺素不会刺激一个单步突变体产生灵菌红素,该突变体在灵菌红素生物合成中表现出与菌株9-3-3相同的表型阻断。这并不奇怪,因为菌株9-3-3是由两个突变事件产生的。一个事件可能直接涉及硫胺素,另一个事件可能涉及MAP的生物合成。硫胺素可能参与了MAP生物合成的调控,因为必须在生长早期添加该维生素或抑制性拮抗剂才能发挥作用。

相似文献

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Prodigiosin synthesis in mutants of Serratia marcesens.粘质沙雷氏菌突变体中灵菌红素的合成
J Bacteriol. 1966 Apr;91(4):1599-604. doi: 10.1128/jb.91.4.1599-1604.1966.

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