Investigation of candidate genes involved in the rhodoquinone biosynthetic pathway in Rhodospirillum rubrum

被引:6
|
作者
Campbell, Amanda R. M. [1 ,3 ]
Titus, Benjamin R. [1 ,4 ]
Kuenzi, Madeline R. [1 ,5 ]
Rodriguez-Perez, Fernando [1 ,6 ]
Brunsch, Alysha D. L. [1 ,7 ]
Schroll, Monica M. [1 ,8 ]
Owen, Matthew C. [1 ,9 ]
Cronk, Jeff D. [1 ]
Anders, Kirk R. [2 ]
Shepherd, Jennifer N. [1 ]
机构
[1] Gonzaga Univ, Dept Chem & Biochem, Spokane, WA 99258 USA
[2] Gonzaga Univ, Dept Biol, Spokane, WA 99258 USA
[3] Univ Washington, Sch Pharm, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Spokane, WA USA
[5] Graham Contracting LTD, Bellevue, WA USA
[6] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
[7] Inland Northwest Blood Ctr, Spokane, WA USA
[8] Hlth Advances, San Francisco, CA USA
[9] La Salle Catholic Coll Preparatory, Milwaukie, OR USA
来源
PLOS ONE | 2019年 / 14卷 / 05期
基金
美国国家卫生研究院;
关键词
FUMARATE REDUCTASE; ELECTRON-TRANSFER; UBIQUINONE; BACTERIUM; EXPRESSION; YEAST;
D O I
10.1371/journal.pone.0217281
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The lipophilic electron-transport cofactor rhodoquinone (RQ) facilitates anaerobic metabolism in a variety of bacteria and selected eukaryotic organisms in hypoxic environments. We have shown that an intact rquA gene in Rhodospirillum rubrum is required for RQ production and efficient growth of the bacterium under anoxic conditions. While the explicit details of RQ biosynthesis have yet to be fully delineated, ubiquinone (Q) is a required precursor to RQ in R. rubrum, and the RquA gene product is homologous to a class I methyltransferase. In order to identify any additional requirements for RQ biosynthesis or factors influencing RQ production in R. rubrum, we performed transcriptome analysis to identify differentially expressed genes in anoxic, illuminated R. rubrum cultures, compared with those aerobically grown in the dark. To further select target genes, we employed a bioinformatics approach to assess the likelihood that a given differentially expressed gene under anoxic conditions may also have a direct role in RQ production or regulation of its levels in vivo. Having thus compiled a list of candidate genes, nine were chosen for further study by generation of knockout strains. RQ and Q levels were quantified using liquid chromatography-mass spectrometry, and rquA gene expression was measured using the real-time quantitative polymerase chain reaction. In one case, Q and RQ levels were decreased relative to wild type; in another case, the opposite effect was observed. These results comport with the crucial roles of rquA and Q in RQ biosynthesis, and reveal the existence of potential modulators of RQ levels in R. rubrum.
引用
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页数:15
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