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缺失突变体在[具体环境]的二次生长转换期间表现出适应性缺陷。

deletion mutants display fitness defects during diauxic shift in .

作者信息

Kowaleski Shane J, Hurmis Christina S, Coleman Carvin N, Philips Kieli D, Najor Nicole A

机构信息

Biology Department, University of Detroit Mercy.

出版信息

MicroPubl Biol. 2023 Jul 28;2023. doi: 10.17912/micropub.biology.000899. eCollection 2023.

DOI:10.17912/micropub.biology.000899
PMID:37577108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10422129/
Abstract

protein She9 is localized to the inner mitochondrial membrane and is required for normal mitochondrial morphology. While deletion mutants of ( ) are viable and display large ring-like mitochondrial structures, the molecular function of is still unknown. We report a decreased growth of cells during a diauxic shift, where mitochondria are primarily employing oxidative phosphorylation to generate ATP versus the alternative mechanism of glycolysis in high glucose conditions. Further bioinformatics analysis reveal putative functional protein associations, and proposes a model to aid in the understanding of the molecular function of She9.

摘要

蛋白质She9定位于线粒体内膜,是正常线粒体形态所必需的。虽然( )的缺失突变体是可行的,并显示出大的环状线粒体结构,但其分子功能仍然未知。我们报告了在二次生长转换期间( )细胞的生长减缓,在此期间线粒体主要利用氧化磷酸化来产生ATP,而在高糖条件下则采用糖酵解的替代机制。进一步的生物信息学分析揭示了假定的功能性蛋白质关联,并提出了一个模型以帮助理解She9的分子功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0873/10422129/f907541852fd/25789430-2023-micropub.biology.000899.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0873/10422129/f907541852fd/25789430-2023-micropub.biology.000899.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0873/10422129/f907541852fd/25789430-2023-micropub.biology.000899.jpg

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本文引用的文献

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The STRING database in 2023: protein-protein association networks and functional enrichment analyses for any sequenced genome of interest.2023 年的 STRING 数据库:针对任何感兴趣的测序基因组的蛋白质-蛋白质关联网络和功能富集分析。
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Pathways shaping the mitochondrial inner membrane.
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