Ktari Amir, Nouioui Imen, Furnholm Teal, Swanson Erik, Ghodhbane-Gtari Faten, Tisa Louis S, Gtari Maher
Laboratoire Microorganismes et Biomolécules Actives, Université Tunis El Manar (FST) & Université de Carthage (INSAT), 2092 Tunis, Tunisia.
Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, 289 Rudman Hall, 46 college Road, Durham, NH 03824-2617 USA.
Stand Genomic Sci. 2017 Sep 4;12:51. doi: 10.1186/s40793-017-0261-3. eCollection 2017.
sp. NRRL B-16219 was directly isolated from a soil sample obtained from the rhizosphere of growing in the USA. Its host plant range includes members of species. Phylogenetically, strain NRRL B-16219 is closely related to " with a 16S rRNA gene similarity of 99.78%. Because of the lack of genetic tools for , our understanding of the bacterial signals involved during the plant infection process and the development of actinorhizal root nodules is very limited. Since the first three genomes were sequenced, additional genome sequences covering more diverse strains have helped provide insight into the depth of the pangenome and attempts to identify bacterial signaling molecules like the rhizobial canonical genes. The genome sequence of sp. strain NRRL B-16219 was generated and assembled into 289 contigs containing 8,032,739 bp with 71.7% GC content. Annotation of the genome identified 6211 protein-coding genes, 561 pseudogenes, 1758 hypothetical proteins and 53 RNA genes including 4 rRNA genes. The NRRL B-16219 draft genome contained genes homologous to the rhizobial common nodulation genes clustered in two areas. The first cluster contains ACIJH genes whereas the second has AB and H genes in the upstream region. Phylogenetic analysis shows that genes are more deeply rooted than their sister groups from rhizobia. PCR-sequencing suggested the widespread occurrence of highly homologous A and B genes in microsymbionts of field collected .
菌株NRRL B - 16219直接从美国采集的生长植物根际土壤样本中分离得到。其寄主植物范围包括某物种的成员。从系统发育角度看,菌株NRRL B - 16219与“某菌”密切相关,16S rRNA基因相似度为99.78%。由于缺乏针对某菌的遗传工具,我们对植物感染过程及放线菌根瘤发育过程中涉及的细菌信号的了解非常有限。自最初三个某菌基因组测序以来,更多不同菌株的基因组序列有助于深入了解泛基因组的深度,并尝试鉴定像根瘤菌典型基因那样的细菌信号分子。某菌菌株NRRL B - 16219的基因组序列被生成并组装成289个重叠群,包含8,032,739 bp,GC含量为71.7%。对该基因组的注释鉴定出6211个蛋白质编码基因、561个假基因、1758个假定蛋白质和53个RNA基因,包括4个rRNA基因。NRRL B - 16219基因组草图包含与根瘤菌常见结瘤基因同源的基因,这些基因聚集在两个区域。第一个簇包含ACIJH基因,而第二个簇在上游区域有AB和H基因。系统发育分析表明,某菌基因比其根瘤菌姐妹群的基因根基更深。PCR测序表明,在田间采集的共生微生物中广泛存在高度同源的A和B基因。