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恶臭假单胞菌KT2440在不同碳源和能源上生长时的蛋白质组分析。

Analysis of the proteome of Pseudomonas putida KT2440 grown on different sources of carbon and energy.

作者信息

Kurbatov Leonid, Albrecht Dirk, Herrmann Heidrun, Petruschka Lothar

机构信息

Ernst-Moritz-Arndt-University, Institute for Microbiology, Department of Genetics and Biochemistry, Greifswald, Germany.

出版信息

Environ Microbiol. 2006 Mar;8(3):466-78. doi: 10.1111/j.1462-2920.2005.00913.x.

DOI:10.1111/j.1462-2920.2005.00913.x
PMID:16478453
Abstract

Using 2D electrophoresis the protein expression pattern during growth on carbon sources with different impact on carbon catabolite repression of phenol degradation was analysed in a derivative of Pseudomonas putida KT2440. The cytosolic protein pattern of cells growing on phenol or the non-repressive substrate pyruvate was almost identical, but showed significant differences to that of cells growing with the repressive substrates succinate or glucose. Proteins, which were mainly expressed in the presence of phenol or pyruvate, could be assigned to the functional groups of transport, detoxification, stress response, amino acid, energy, carbohydrate and nucleotide metabolism. The addition of succinate to cells growing with phenol ('shift-up') resulted in the inhibition of the synthesis of these proteins. Proteins with enhanced expression at growth with succinate or glucose were proteins for de novo synthesis of nucleotides, amino acids and enzymes of the TCA cycle. The synthesis of proteins, necessary for phenol catabolism was regulated in different manners following the addition of succinate. Whereas the synthesis of Phl-proteins (subunits of the phenolhydroxylase) only decreased slowly, was the translation of the Cat-proteins (catechol 1,2-dioxygenase, cis,cis-muconate cycloisomerase and muconolactone isomerase) repressed immediately and the synthesis of the Pca-proteins (beta-ketoadipate enolactone hydrolase, beta-ketoadipate succinyl-CoA transferase and beta-ketoadipyl CoA thiolase) remained unaffected.

摘要

利用二维电泳技术,在恶臭假单胞菌KT2440的一个衍生物中分析了在对苯酚降解的碳分解代谢阻遏有不同影响的碳源上生长期间的蛋白质表达模式。在苯酚或非阻遏性底物丙酮酸上生长的细胞的胞质蛋白质模式几乎相同,但与在阻遏性底物琥珀酸或葡萄糖上生长的细胞的蛋白质模式有显著差异。主要在苯酚或丙酮酸存在时表达的蛋白质可归为运输、解毒、应激反应、氨基酸、能量、碳水化合物和核苷酸代谢等功能组。向以苯酚生长的细胞中添加琥珀酸(“上调转换”)导致这些蛋白质的合成受到抑制。在以琥珀酸或葡萄糖生长时表达增强的蛋白质是用于核苷酸、氨基酸从头合成以及三羧酸循环酶的蛋白质。添加琥珀酸后,苯酚分解代谢所需蛋白质的合成以不同方式受到调节。虽然Phl蛋白(苯酚羟化酶的亚基)的合成仅缓慢下降,但Cat蛋白(儿茶酚1,2-双加氧酶、顺,顺-粘康酸环异构酶和粘康内酯异构酶)的翻译立即受到抑制,而Pca蛋白(β-酮己二酸烯醇内酯水解酶、β-酮己二酸琥珀酰辅酶A转移酶和β-酮己二酰辅酶A硫解酶)的合成不受影响。

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