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从铜绿假单胞菌中鉴定出一种包含柠檬酸合酶同工酶的三羧酸循环酶多酶复合物。

Identification of a multienzyme complex of the tricarboxylic acid cycle enzymes containing citrate synthase isoenzymes from Pseudomonas aeruginosa.

作者信息

Mitchell C G

机构信息

Department of Biological Sciences, Napier University, Edinburgh, Scotland, U.K.

出版信息

Biochem J. 1996 Feb 1;313 ( Pt 3)(Pt 3):769-74. doi: 10.1042/bj3130769.

Abstract

A multienzyme complex of tricarboxylic acid cycle enzymes, catalysing the consecutive reactions from fumarate to 2-oxoglutarate, has been identified in extracts of Pseudomonas aeruginosa prepared by gentle osmotic lysis of the cells. The individual enzyme activities of fumarase, malate dehydrogenase, citrate synthase, aconitase and isocitrate dehydrogenase can be used to reconstitute the complex. The citrate synthase isoenzymes, CSI and CSII, from this organism can be used either together or as the individual activities to reconstitute the complex. No complex can be reformed in the absence of CSI or CSII. Which CS isoenzyme predominates in the complex depends on the phase of growth at which the cells were harvested and the extract prepared. More CSI was found in the complex during exponential growth, whereas CSII predominated during the stationary phase. The results support the idea of a 'metabolon' in this organism, with the composition of the CS component varying during the growth cycle.

摘要

在通过对铜绿假单胞菌细胞进行温和渗透裂解制备的提取物中,已鉴定出一种三羧酸循环酶的多酶复合物,它催化从富马酸盐到2-氧代戊二酸的连续反应。富马酸酶、苹果酸脱氢酶、柠檬酸合酶、乌头酸酶和异柠檬酸脱氢酶的各个酶活性可用于重组该复合物。来自该生物体的柠檬酸合酶同工酶CSI和CSII可一起使用,也可作为单独的活性用于重组该复合物。在没有CSI或CSII的情况下无法重新形成复合物。复合物中哪种CS同工酶占主导取决于收获细胞和制备提取物时的生长阶段。在指数生长期间,复合物中发现更多的CSI,而在稳定期CSII占主导。结果支持了该生物体中存在“代谢体”的观点,即CS成分的组成在生长周期中会发生变化。

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本文引用的文献

1
Starch-gel electrophoresis of malate dehydrogenase.苹果酸脱氢酶的淀粉凝胶电泳
Biochim Biophys Acta. 1963 Jun 11;73:193-203. doi: 10.1016/0006-3002(63)90303-2.
2
Does Escherichia coli possess a second citrate synthase gene?
Eur J Biochem. 1993 May 15;214(1):75-81. doi: 10.1111/j.1432-1033.1993.tb17898.x.
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Demonstration of enzyme associations by countermigration electrophoresis in agarose gel.
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