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Uptake of Biotin by Chlamydia Spp. through the Use of a Bacterial Transporter (BioY) and a Host-Cell Transporter (SMVT)

机译:由衣原体属摄取生物素。通过使用细菌转运蛋白(BioY)和宿主细胞转运(smVT)

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摘要

Chlamydia spp. are obligate intracellular Gram-negative bacterial pathogens that cause disease in humans and animals. Minor variations in metabolic capacity between species have been causally linked to host and tissue tropisms. Analysis of the highly conserved genomes of Chlamydia spp. reveals divergence in the metabolism of the essential vitamin biotin with genes for either synthesis (bioF_2ADB) and/or transport (bioY). Streptavidin blotting confirmed the presence of a single biotinylated protein in Chlamydia. As a first step in unraveling the need for divergent biotin acquisition strategies, we examined BioY (CTL0613) from C. trachomatis 434/Bu which is annotated as an S component of the type II energy coupling-factor transporters (ECF). Type II ECFs are typically composed of a transport specific component (S) and a chromosomally unlinked energy module (AT). Intriguingly, Chlamydia lack recognizable AT modules. Using 3H-biotin and recombinant E. coli expressing CTL0613, we demonstrated that biotin was transported with high affinity (a property of Type II ECFs previously shown to require an AT module) and capacity (apparent K(m) of 3.35 nM and V(max) of 55.1 pmol×min−1×mg−1). Since Chlamydia reside in a host derived membrane vacuole, termed an inclusion, we also sought a mechanism for transport of biotin from the cell cytoplasm into the inclusion vacuole. Immunofluorescence microscopy revealed that the mammalian sodium multivitamin transporter (SMVT), which transports lipoic acid, biotin, and pantothenic acid into cells, localizes to the inclusion. Since Chlamydia also are auxotrophic for lipoic and pantothenic acids, SMVT may be subverted by Chlamydia to move multiple essential compounds into the inclusion where BioY and another transporter(s) would be present to facilitate transport into the bacterium. Collectively, our data validates the first BioY from a pathogenic organism and describes a two-step mechanism by which Chlamydia transport biotin from the host cell into the bacterial cytoplasm.
机译:衣原体是专一的导致人类和动物疾病的细胞内革兰氏阴性细菌病原体。物种之间代谢能力的微小变化与宿主和组织的向性有因果关系。衣原体高度保守的基因组分析。揭示必需维生素生物素的代谢与合成(bioF_2ADB)和/或转运(bioY)的基因存在差异。链霉亲和素印迹证实衣原体中存在单个生物素化蛋白。作为阐明对不同生物素获取策略的需求的第一步,我们检查了来自沙眼衣原体434 / Bu的BioY(CTL0613),其被标注为II型能量耦合因子转运子(ECF)的S成分。 II型ECF通常由运输特定成分(S)和染色体未连接的能量模块(AT)组成。有趣的是,衣原体缺乏可识别的AT模块。使用 3 H-生物素和表达CTL0613的重组大肠杆菌,我们证明了生物素的运输具有很高的亲和力(II型ECF的特性先前显示需要AT模块)和容量(表观K( m)为3.35 nM,V(max)为55.1 pmol×min -1 ×mg -1 。由于衣原体位于宿主衍生的膜液泡(称为包涵体)中,我们还寻求了一种将生物素从细胞质转运到包膜液泡中的机制。免疫荧光显微镜检查显示,将硫辛酸,生物素和泛酸转运到细胞中的哺乳动物多种维生素钠转运蛋白(SMVT)定位于包裹体中。由于衣原体对于硫辛酸和泛酸也是营养缺陷的,因此衣原体可能会将SMVT破坏,从而将多种必需化合物转移到包含BioY和其他转运蛋白的包裹体中,以利于转运到细菌中。总的来说,我们的数据验证了来自致病生物的第一个BioY,并描述了衣原体将生物素从宿主细胞转运到细菌细胞质的两步机制。

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