首页> 美国卫生研究院文献>Journal of Bacteriology >The Presumptive Magnetosome Protein Mms16 Is a Poly(3-Hydroxybutyrate) Granule-Bound Protein (Phasin) in Magnetospirillum gryphiswaldense
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The Presumptive Magnetosome Protein Mms16 Is a Poly(3-Hydroxybutyrate) Granule-Bound Protein (Phasin) in Magnetospirillum gryphiswaldense

机译:假定的磁小体蛋白Mms16是在Magspirospirillum gryphiswaldense中的一种聚(3-羟基丁酸酯)颗粒结合蛋白(Phasin)。

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摘要

The Mms16 protein has been previously found to be associated with isolated magnetosomes from two Magnetospirillum strains. A function of this protein as a magnetosome-specific GTPase involved in the formation of intracellular magnetosome membrane vesicles was suggested (Y. Okamura, H. Takeyama, and T. Matsunaga, J. Biol. Chem. >276:48183-48188, 2001). Here we present a study of the Mms16 protein from Magnetospirillum gryphiswaldense to clarify its function. Insertion-duplication mutagenesis of the mms16 gene did not affect the formation of magnetosome particles but resulted in the loss of the ability of M. gryphiswaldense cell extracts to activate poly(3-hydroxybutyrate) (PHB) depolymerization in vitro, which was coincident with loss of the most abundant 16-kDa polypeptide from preparations of PHB granule-bound proteins. The mms16 mutation could be functionally complemented by enhanced yellow fluorescent protein (EYFP) fused to ApdA, which is a PHB granule-bound protein (phasin) in Rhodospirillum rubrum sharing 55% identity to Mms16. Fusions of Mms16 and ApdA to enhanced green fluorescent protein (EGFP) or EYFP were colocalized in vivo with the PHB granules but not with the magnetosome particles after conjugative transfer to M. gryphiswaldense. Although the Mms16-EGFP fusion protein became detectable by Western analysis in all cell fractions upon cell disruption, it was predominantly associated with isolated PHB granules. Contrary to previous suggestions, our results argue against an essential role of Mms16 in magnetosome formation, and the previously observed magnetosome localization is likely an artifact due to unspecific adsorption during preparation. Instead, we conclude that Mms16 in vivo is a PHB granule-bound protein (phasin) and acts in vitro as an activator of PHB hydrolysis by R. rubrum PHB depolymerase PhaZ1. Accordingly, we suggest renaming the Mms16 protein of Magnetospirillum species to ApdA, as in R. rubrum.
机译:以前已经发现Mms16蛋白与来自两个磁螺旋体菌株的分离的磁小体有关。有人提出,这种蛋白质作为磁小体特异性GTP酶的功能参与细胞内磁小体膜小泡的形成(Y. Okamura,H。Takeyama和T. Matsunaga,J。Biol。Chem。> 276: 48183-48188,2001)。在这里,我们提出了对来自Magspirospirillum gryphiswaldense的Mms16蛋白的研究,以阐明其功能。 mms16基因的插入-重复诱变不会影响磁小体颗粒的形成,但会导致格氏疟原虫细胞提取物在体外激活聚(3-羟基丁酸酯)(PHB)解聚的能力丧失,这与丢失相吻合。 PHB颗粒结合蛋白制品中最丰富的16-kDa多肽mms16突变可以通过与ApdA融合的增强型黄色荧光蛋白(EYFP)在功能上进行补充,这是一种在红螺螺旋藻中与Mms16共享55%同一性的PHB颗粒结合蛋白(phasin)。 Mms16和ApdA与增强型绿色荧光蛋白(EGFP)或EYFP的融合体在体内共定位转移至格氏疟原虫后,与PHB颗粒共定位于体内,但与磁小体颗粒共定位于体内。尽管通过细胞分裂后的所有细胞组分均可以通过Western分析检测到Mms16-EGFP融合蛋白,但它主要与分离的PHB颗粒有关。与以前的建议相反,我们的研究结果反对Mms16在磁小体形成中的重要作用,并且由于制备过程中的非特异性吸附,先前观察到的磁小体定位很可能是伪影。取而代之的是,我们得出的结论是Mms16在体内是一种PHB颗粒结合蛋白(phasin),并且在体外起着R. rubrum PHB解聚酶PhaZ1对PHB水解的激活作用。因此,我们建议将红螺螺菌种的Mms16蛋白重命名为ApdA,就像在红红霉菌中一样。

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