Si Yuan-Yuan, Xu Kai-Hang, Yu Xiang-Yong, Wang Mei-Fang, Chen Xing-Han
a College of Fisheries, Guangdong Ocean University, Zhanjiang, 524025, People's Republic of China.
b Key Laboratory for Marine Estuary Fishery Resources Protection of Yangjiang, Department of Food and Environmental Engineering, Yangjiang Polytechnic, Yangjiang, 529566, People's Republic of China.
Can J Microbiol. 2019 Jul;65(7):486-495. doi: 10.1139/cjm-2019-0037. Epub 2019 Mar 21.
Studies show that can denitrify nitrogen sources under aerobic conditions. However, the lack of data on its genome sequence has restricted molecular studies and practical applications. In this study, the complete genome of ATCC 19367 was sequenced and its nitrogen metabolism properties were characterized. The size of the whole genome is 5 242 327 bp, with two chromosomes and one plasmid. The average G + C content is 66.8%, and it contains 5308 protein-coding genes, 54 tRNA genes, and nine rRNA operons. Among the protein-coding genes, 71.35% could be assigned to the Gene Ontology (GO) pathway, 86.66% to the Clusters of Orthologous Groups (COG) pathway, and 50.57% to the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway. Comparative genome analysis between ATCC 19367 and PD1222 revealed that there are 428 genes specific to ATCC 19367 and 4738 core genes. Furthermore, the expression of genes related to denitrification, biofilm formation, and nitrogen metabolism (, , and ) by ATCC 19367 under aerobic conditions was affected by incubation time and shaking speed. This study elucidates the genomic background of ATCC 19367 and suggests the possibility of controlling nitrogen pollution in the environment by using this bacterium.
研究表明,[细菌名称]在有氧条件下可使氮源反硝化。然而,其基因组序列数据的缺乏限制了分子研究和实际应用。在本研究中,对[细菌名称]ATCC 19367的全基因组进行了测序,并对其氮代谢特性进行了表征。全基因组大小为5 242 327 bp,有两条染色体和一个质粒。平均G + C含量为66.8%,包含5308个蛋白质编码基因、54个tRNA基因和9个rRNA操纵子。在蛋白质编码基因中,71.35%可归入基因本体论(GO)途径,86.66%可归入直系同源簇(COG)途径,50.57%可归入京都基因与基因组百科全书(KEGG)途径。对[细菌名称]ATCC 19367和[细菌名称]PD1222的比较基因组分析表明,ATCC 19367有428个特异性基因和4738个核心基因。此外,[细菌名称]ATCC 19367在有氧条件下与反硝化、生物膜形成和氮代谢相关的基因([基因名称1]、[基因名称2]和[基因名称3])的表达受培养时间和振荡速度的影响。本研究阐明了[细菌名称]ATCC 19367的基因组背景,并提出了利用该细菌控制环境中氮污染的可能性。