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普氏栖瘤胃菌中的葡萄糖毒性:甲基乙二醛积累及其对膜生理学的影响。

Glucose toxicity in Prevotella ruminicola: methylglyoxal accumulation and its effect on membrane physiology.

作者信息

Russell J B

机构信息

Agricultural Research Service, Cornell University, Ithaca, New York 14853-8101.

出版信息

Appl Environ Microbiol. 1993 Sep;59(9):2844-50. doi: 10.1128/aem.59.9.2844-2850.1993.

Abstract

When the ruminal bacterium prevotella ruminicola B(1)4-M was grown in a defined medium with an excess of glucose (3.6 mM ammonia and 50 mM glucose), the cells accumulated large amounts of cellular polysaccharide and the viable cell number decreased at least 1,000-fold. This decrease in viability was correlated with an accumulation of methylglyoxal in the supernatant (3 to 4 mM). Other genetically distinct strains of P. ruminicola produced methylglyoxal, but methylglyoxal production was not ubiquitous among the strains. When P. ruminicola B(1)4-M was grown in continuous culture (dilution rate, 0.1 h-1) with an excess of glucose, there was an oscillating pattern of growth and cell death which was correlated with the accumulation and washout of methylglyoxal from the culture vessel. Mutants which resisted an excess of glucose took up glucose at a slower rate and produced less methylglyoxal than the wild type. These mutants were, however, not stable. There was always a long lag time, and the mutants could only be maintained with a daily transfer schedule. When the mutants were transferred less frequently, methylglyoxal eventually accumulated and the cultures died. The mutants transported glucose at a threefold-slower rate than the wild type, and in each case the carrier had more than one binding site for glucose. Because glucose transport could not be driven by phosphoenolpyruvate or ATP, the glucose carrier of P. ruminicola is probably a proton symport system. When P. ruminicola B(1)4-M cultures were treated with 4 mM methylglyoxal, the delta psi decreased even though intracellular ATP concentrations were high.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

当瘤胃细菌普氏瘤胃菌B(1)4 - M在含有过量葡萄糖(3.6 mM氨和50 mM葡萄糖)的限定培养基中生长时,细胞积累了大量的胞内多糖,活细胞数量至少减少了1000倍。活力的这种下降与上清液中甲基乙二醛的积累(3至4 mM)相关。其他遗传上不同的普氏瘤胃菌菌株也产生甲基乙二醛,但甲基乙二醛的产生在这些菌株中并非普遍存在。当普氏瘤胃菌B(1)4 - M在连续培养(稀释率为0.1 h⁻¹)且有过量葡萄糖的条件下生长时,出现了生长和细胞死亡的振荡模式,这与甲基乙二醛在培养容器中的积累和洗脱相关。抵抗过量葡萄糖的突变体摄取葡萄糖的速度较慢,产生的甲基乙二醛比野生型少。然而,这些突变体不稳定。总是有很长的延迟期,并且这些突变体只能通过每日传代方案来维持。当突变体传代频率较低时,甲基乙二醛最终会积累,培养物死亡。突变体转运葡萄糖的速度比野生型慢三倍,并且在每种情况下载体对葡萄糖都有不止一个结合位点。由于葡萄糖转运不能由磷酸烯醇丙酮酸或ATP驱动,普氏瘤胃菌的葡萄糖载体可能是一种质子同向转运系统。当用4 mM甲基乙二醛处理普氏瘤胃菌B(1)4 - M培养物时,即使细胞内ATP浓度很高,Δψ也会降低。(摘要截断于250字)

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