Wang, Fengping


Publications
4

Globally distributed Myxococcota with photosynthesis gene clusters illuminate the origin and evolution of a potentially chimeric lifestyle

Citation
Li et al. (2023). Nature Communications 14 (1)
Names
“Houyibacterium oceanica” “Houyibacterium” “Houyibacteriaceae” “Houyihalomonas phototrophica” “Xihehalomonas phototrophica” “Xihemonas sinensis” “Kuafubacteria” “Kuafubacterium phototrophica” “Kuafucaenimonas phototrophica” “Kuafuhalomonas phototrophica” “Xihepedomonas phototrophica” “Xihelimnomonas phototrophica” “Xihecaenimonas phototrophica” “Kuafubacteriales” “Kuafubacteriaceae” “Xihehalomonas” “Xihemonas” “Xihecaenibacterium” “Houyihalomonas” “Xihelimnobacterium phototrophica” “Xihelimnobacterium” “Xihemonas phototrophica” “Xihecaenibacterium phototrophica” “Xihebacterium phototrophica” “Xihebacterium glacialis” “Xihebacterium aquatica” “Xihemicrobium phototrophica” “Xihemicrobium aquatica” “Kuafubacterium” “Xihebacterium” “Xihemicrobium” “Xihecaenimonas” “Xihelimnomonas” “Xihepedomonas” “Kuafuhalomonas” “Kuafucaenimonas”
Abstract
AbstractPhotosynthesis is a fundamental biogeochemical process, thought to be restricted to a few bacterial and eukaryotic phyla. However, understanding the origin and evolution of phototrophic organisms can be impeded and biased by the difficulties of cultivation. Here, we analyzed metagenomic datasets and found potential photosynthetic abilities encoded in the genomes of uncultivated bacteria within the phylum Myxococcota. A putative photosynthesis gene cluster encoding a type-II reaction cent