Kofoid E, Rappleye C, Stojiljkovic I, Roth J
Department of Biology, University of Utah, Salt Lake City, Utah 84112, USA.
J Bacteriol. 1999 Sep;181(17):5317-29. doi: 10.1128/JB.181.17.5317-5329.1999.
The eut operon of Salmonella typhimurium encodes proteins involved in the cobalamin-dependent degradation of ethanolamine. Previous genetic analysis revealed six eut genes that are needed for aerobic use of ethanolamine; one (eutR), encodes a positive regulator which mediates induction of the operon by vitamin B12 plus ethanolamine. The DNA sequence of the eut operon included 17 genes, suggesting a more complex pathway than that revealed genetically. We have correlated an open reading frame in the sequence with each of the previously identified genes. Nonpolar insertion and deletion mutations made with the Tn10-derived transposable element T-POP showed that at least 10 of the 11 previously undetected eut genes have no Eut phenotype under the conditions tested. Of the dispensable eut genes, five encode apparent homologues of proteins that serve (in other organisms) as shell proteins of the carboxysome. This bacterial organelle, found in photosynthetic and sulfur-oxidizing bacteria, may contribute to CO2 fixation by concentrating CO2 and excluding oxygen. The presence of these homologues in the eut operon of Salmonella suggests that CO2 fixation may be a feature of ethanolamine catabolism in Salmonella.
鼠伤寒沙门氏菌的eut操纵子编码参与钴胺素依赖性乙醇胺降解的蛋白质。先前的遗传分析揭示了需氧利用乙醇胺所需的六个eut基因;其中一个基因(eutR)编码一种正调控因子,该调控因子介导维生素B12加乙醇胺对操纵子的诱导作用。eut操纵子的DNA序列包含17个基因,这表明其途径比遗传分析所揭示的更为复杂。我们已将序列中的一个开放阅读框与每个先前鉴定的基因相关联。用源自Tn10的转座元件T-POP进行的非极性插入和缺失突变表明,在测试条件下,11个先前未检测到的eut基因中至少有10个没有Eut表型。在这些可有可无的eut基因中,有五个编码(在其他生物体中)作为羧酶体外壳蛋白的蛋白质的明显同源物。这种存在于光合细菌和硫氧化细菌中的细菌细胞器,可能通过浓缩二氧化碳和排除氧气来促进二氧化碳固定。鼠伤寒沙门氏菌的eut操纵子中存在这些同源物表明,二氧化碳固定可能是鼠伤寒沙门氏菌乙醇胺分解代谢的一个特征。