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鼠伤寒沙门氏菌对α-酮酸的铁调节排泄

Iron-regulated excretion of alpha-keto acids by Salmonella typhimurium.

作者信息

Reissbrodt R, Kingsley R, Rabsch W, Beer W, Roberts M, Williams P H

机构信息

Robert Koch Institute, Wernigerode Branch, Germany.

出版信息

J Bacteriol. 1997 Jul;179(14):4538-44. doi: 10.1128/jb.179.14.4538-4544.1997.

Abstract

Excretion of alpha-keto acids by clinical isolates and laboratory strains of Salmonella typhimurium was determined by high-performance liquid chromatography analysis of culture supernatants. The levels of excretion increased markedly with increasing iron stress imposed by the presence of alpha,alpha'-dipyridyl or conalbumin in the medium. The major product was pyruvic acid, but significant concentrations of alpha-ketoglutaric acid, alpha-ketoisovaleric acid, and alpha-ketoisocaproic acid were also observed. Maximal excretion occurred at iron stress levels that initially inhibited bacterial growth; the concentration of alpha,alpha'-dipyridyl at which this was observed differed between strains depending on their ability to secrete and utilize siderophores, suggesting that the intracellular iron status was important in determining alpha-keto acid excretion. However, prolonged incubation of the siderophore-deficient S. typhimurium strain enb-7 under conditions of high iron stress resulted in significant delayed bacterial growth, promoted by tonB-dependent uptake of iron complexed with the high accumulated levels of pyruvic acid and other alpha-keto acids. Strain RB181, a fur derivative of enb-7, excreted massive amounts of alpha-keto acids into the culture medium even in the absence of any iron chelators (the concentration of pyruvic acid, for example, was >25 mM). Moreover, RB181 was able to grow and excrete alpha-keto acids in the presence of alpha,alpha'-dipyridyl at concentrations threefold greater than that which inhibited the growth of enb-7.

摘要

通过对培养上清液进行高效液相色谱分析,测定了鼠伤寒沙门氏菌临床分离株和实验室菌株中α-酮酸的排泄情况。随着培养基中α,α'-联吡啶或运铁蛋白的存在所施加的铁应激增加,排泄水平显著升高。主要产物是丙酮酸,但也观察到了显著浓度的α-酮戊二酸、α-酮异戊酸和α-酮异己酸。最大排泄量出现在最初抑制细菌生长的铁应激水平;观察到这一现象时α,α'-联吡啶的浓度因菌株分泌和利用铁载体的能力不同而有所差异,这表明细胞内铁状态在决定α-酮酸排泄方面很重要。然而,在高铁应激条件下,对缺乏铁载体的鼠伤寒沙门氏菌菌株enb-7进行长时间培养,导致细菌生长显著延迟,这是由tonB依赖性摄取与高积累水平的丙酮酸和其他α-酮酸络合的铁所促进的。菌株RB181是enb-7的fur衍生物,即使在没有任何铁螯合剂的情况下,也会向培养基中大量排泄α-酮酸(例如,丙酮酸浓度>25 mM)。此外,在α,α'-联吡啶浓度比抑制enb-7生长的浓度高三倍的情况下,RB181仍能够生长并排泄α-酮酸。

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