Pyridoxal 5'-phosphate synthesis and salvage in Bacteria and Archaea: predicting pathway variant distributions and holes

被引:11
作者
Denise, Remi [1 ,4 ]
Babor, Jill [1 ]
Gerlt, John A. [2 ]
de Crecy-Lagard, Valerie [1 ,3 ]
机构
[1] Univ Florida, Dept Microbiol & Cell Sci, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[3] Univ Florida, Genet Inst, Gainesville, FL 32611 USA
[4] Univ Cork, APC Microbiome Ireland, Cork, Ireland
来源
MICROBIAL GENOMICS | 2023年 / 9卷 / 02期
基金
美国国家卫生研究院;
关键词
B6; vitamers; Hidden Markov models; pyridoxal; pyridoxine; sequence similarity networks; VITAMIN-B-6; BIOSYNTHESIS; BACILLUS-SUBTILIS; PHOSPHATE BIOSYNTHESIS; COMPARATIVE GENOMICS; METABOLIC PATHWAYS; KINASE FAMILY; PDXR; IDENTIFICATION; GENE; 5'-PHOSPHATE;
D O I
10.1099/mgen.0.000926
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Pyridoxal 5'-phosphate or PLP is a cofactor derived from B6 vitamers and essential for growth in all known organisms. PLP synthesis and salvage pathways are well characterized in a few model species even though key components, such as the vitamin B6 transporters, are still to be identified in many organisms including the model bacteria Escherichia coli or Bacillus subtilis. Using a comparative genomic approach, PLP synthesis and salvage pathways were predicted in 5840 bacterial and archaeal species with complete genomes. The distribution of the two known de novo biosynthesis pathways and previously identified cases of non-orthologous displacements were surveyed in the process. This analysis revealed that several PLP de novo pathway genes remain to be identified in many organisms, either because sequence similarity alone cannot be used to discriminate among several homologous candidates or due to non-orthologous displacements. Candidates for some of these pathway holes were identified using published TnSeq data, but many remain. We find that similar to 10 % of the analysed organisms rely on salvage but further analyses will be required to identify potential transporters. This work is a starting point to model the exchanges of B6 vitamers in communities, predict the sensitivity of a given organism to drugs targeting PLP synthesis enzymes, and identify numerous gaps in knowledge that will need to be tackled in the years to come.
引用
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页数:13
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