首页> 外文OA文献 >PduA Is a Shell Protein of Polyhedral Organelles Involved in Coenzyme B12-Dependent Degradation of 1,2-Propanediol in Salmonella enterica Serovar Typhimurium LT2†
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PduA Is a Shell Protein of Polyhedral Organelles Involved in Coenzyme B12-Dependent Degradation of 1,2-Propanediol in Salmonella enterica Serovar Typhimurium LT2†

机译:PduA是涉及肠炎沙门氏菌鼠伤寒沙门氏菌LT2†中辅酶B12依赖的1,2-丙二醇降解的多面体细胞器壳蛋白。

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摘要

Salmonella enterica forms polyhedral organelles involved in coenzyme B12-dependent 1,2-propanediol degradation. These organelles are thought to consist of a proteinaceous shell that encases coenzyme B12-dependent diol dehydratase and perhaps other enzymes involved in 1,2-propanediol degradation. The function of these organelles is unknown, and no detailed studies of their structure have been reported. Genes needed for organelle formation and for 1,2-propanediol degradation are located at the 1,2-propanediol utilization (pdu) locus, but the specific genes involved in organelle formation have not been identified. Here, we show that the pduA gene encodes a shell protein required for the formation of polyhedral organelles involved in coenzyme B12-dependent 1,2-propanediol degradation. A His6-PduA fusion protein was purified from a recombinant Escherichia coli strain and used for the preparation of polyclonal antibodies. The anti-PduA antibodies obtained were partially purified by a subtraction procedure and used to demonstrate that the PduA protein localized to the shell of the polyhedral organelles. In addition, electron microscopy studies established that strains with nonpolar pduA mutations were unable to form organelles. These results show that the pduA gene is essential for organelle formation and indicate that the PduA protein is a structural component of the shell of these organelles. Physiological studies of nonpolar pduA mutants were also conducted. Such mutants grew similarly to the wild-type strain at low concentrations of 1,2-propanediol but exhibited a period of interrupted growth in the presence of higher concentrations of this growth substrate. Growth tests also showed that a nonpolar pduA deletion mutant grew faster than the wild-type strain at low vitamin B12 concentrations. These results suggest that the polyhedral organelles formed by S. enterica during growth on 1,2-propanediol are not involved in the concentration of 1,2-propanediol or coenzyme B12, but are consistent with the hypothesis that these organelles moderate aldehyde production to minimize toxicity.
机译:肠炎沙门氏菌形成多面体细胞器,参与辅酶B12依赖的1,2-丙二醇降解。这些细胞器被认为由蛋白质外壳构成,该外壳包裹着辅酶B12依赖性二醇脱水酶,以及可能参与1,2-丙二醇降解的其他酶。这些细胞器的功能尚不清楚,尚未报道其结构的详细研究。细胞器形成和1,2-丙二醇降解所需的基因位于1,2-丙二醇利用(pdu)位点,但尚未确定参与细胞器形成的特定基因。在这里,我们表明pduA基因编码参与参与辅酶B12依赖的1,2-丙二醇降解的多面体细胞器形成所需的壳蛋白。从重组大肠杆菌菌株中纯化His6-PduA融合蛋白,并用于制备多克隆抗体。获得的抗PduA抗体通过减法部分纯化,并用于证明PduA蛋白定位于多面体细胞器的外壳。此外,电子显微镜研究确定具有非极性pduA突变的菌株无法形成细胞器。这些结果表明pduA基因对于细胞器的形成是必不可少的,并且表明PduA蛋白是这些细胞器的壳的结构成分。还进行了非极性pduA突变体的生理研究。这些突变体在低浓度的1,2-丙二醇中与野生型菌株相似地生长,但是在较高浓度的该生长底物存在下表现出中断的生长时期。生长测试还表明,在低维生素B12浓度下,非极性pduA缺失突变体的生长速度快于野生型菌株。这些结果表明,由肠炎沙门氏菌在1,2-丙二醇上生长期间形成的多面体细胞器不参与1,2-丙二醇或辅酶B12的浓度,但与这些细胞器调节醛生成以最小化醛的假设相一致。毒性。

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