Draft genome sequences of Bradyrhizobium shewense sp. nov. ERR11T and Bradyrhizobium yuanmingense CCBAU 10071T.

Q3 Biochemistry, Genetics and Molecular Biology
Standards in Genomic Sciences Pub Date : 2017-12-05 eCollection Date: 2017-01-01 DOI:10.1186/s40793-017-0283-x
Aregu Amsalu Aserse, Tanja Woyke, Nikos C Kyrpides, William B Whitman, Kristina Lindström
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引用次数: 23

Abstract

The type strain of the prospective 10.1601/nm.30737 sp. nov. ERR11T, was isolated from a nodule of the leguminous tree Erythrina brucei native to Ethiopia. The type strain 10.1601/nm.1463 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+10071 T, was isolated from the nodules of Lespedeza cuneata in Beijing, China. The genomes of ERR11T and 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+10071 T were sequenced by DOE-JGI and deposited at the DOE-JGI genome portal as well as at the European Nucleotide Archive. The genome of ERR11T is 9,163,226 bp in length and has 102 scaffolds, containing 8548 protein-coding and 86 RNA genes. The 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+10071 T genome is arranged in 108 scaffolds and consists of 8,201,522 bp long and 7776 protein-coding and 85 RNA genes. Both genomes contain symbiotic genes, which are homologous to the genes found in the complete genome sequence of 10.1601/nm.24498 10.1601/strainfinder?urlappend=%3Fid%3DUSDA+110 T. The genes encoding for nodulation and nitrogen fixation in ERR11T showed high sequence similarity with homologous genes found in the draft genome of peanut-nodulating 10.1601/nm.27386 10.1601/strainfinder?urlappend=%3Fid%3DLMG+26795 T. The nodulation genes nolYA-nodD2D1YABCSUIJ-nolO-nodZ of ERR11T and 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+10071 T are organized in a similar way to the homologous genes identified in the genomes of 10.1601/strainfinder?urlappend=%3Fid%3DUSDA+110 T, 10.1601/nm.25806 10.1601/strainfinder?urlappend=%3Fid%3DUSDA+4 and 10.1601/nm.1462 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+05525. The genomes harbor hupSLCFHK and hypBFDE genes that code the expression of hydrogenase, an enzyme that helps rhizobia to uptake hydrogen released by the N2-fixation process and genes encoding denitrification functions napEDABC and norCBQD for nitrate and nitric oxide reduction, respectively. The genome of ERR11T also contains nosRZDFYLX genes encoding nitrous oxide reductase. Based on multilocus sequence analysis of housekeeping genes, the novel species, which contains eight strains formed a unique group close to the 10.1601/nm.25806 branch. Genome Average Nucleotide Identity (ANI) calculated between the genome sequences of ERR11T and closely related sequences revealed that strains belonging to 10.1601/nm.25806 branch (10.1601/strainfinder?urlappend=%3Fid%3DUSDA+4 and 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+15615), were the closest strains to the strain ERR11T with 95.2% ANI. Type strain ERR11T showed the highest DDH predicted value with 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+15615 (58.5%), followed by 10.1601/strainfinder?urlappend=%3Fid%3DUSDA+4 (53.1%). Nevertheless, the ANI and DDH values obtained between ERR11T and 10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+15615 or 10.1601/strainfinder?urlappend=%3Fid%3DUSDA+4 were below the cutoff values (ANI ≥ 96.5%; DDH ≥ 70%) for strains belonging to the same species, suggesting that ERR11T is a new species. Therefore, based on the phylogenetic analysis, ANI and DDH values, we formally propose the creation of 10.1601/nm.30737 sp. nov. with strain ERR11T (10.1601/strainfinder?urlappend=%3Fid%3DHAMBI+3532 T=10.1601/strainfinder?urlappend=%3Fid%3DLMG+30162 T) as the type strain.

Abstract Image

Abstract Image

Abstract Image

绘制沈氏慢生根瘤菌ERR11T和远明ense慢生根瘤菌CCBAU 10071T基因组序列。
预期菌株类型为10.1601/nm。30737 sp. 11 . ERR11T是从原产于埃塞俄比亚的豆科树Erythrina brucei的一个根瘤中分离出来的。型应变为10.1601/nm。1463 10.1601 / strainfinder ?urlappend=%3Fid%3DCCBAU+10071 T是从中国北京地区胡枝子根瘤中分离得到的。ERR11T和10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+10071 T由DOE-JGI测序,并保存在DOE-JGI基因组门户网站和欧洲核苷酸档案馆。ERR11T基因组全长9163226 bp,有102个支架,包含8548个蛋白编码基因和86个RNA基因。10.1601 / strainfinder吗?urlappend=%3Fid%3DCCBAU+10071 T基因组排列在108个支架中,由8,201,522 bp长,7776个蛋白质编码基因和85个RNA基因组成。两个基因组都含有共生基因,这些基因与10.1601/nm的全基因组序列中的基因同源。24498 10.1601 / strainfinder ?ERR11T中编码花生结瘤和固氮的基因与花生结瘤基因草图(10.1601/nm)中的同源基因序列具有高度的相似性。27386 10.1601 / strainfinder ?ERR11T和10.1601/strainfinder的结瘤基因nolYA-nodD2D1YABCSUIJ-nolO-nodZ它们的组织方式与10.1601/strainfinder?urlappend=%3Fid%3DUSDA+110 T, 10.1601/nm。25806 10.1601 / strainfinder ?urlappend=%3Fid%3DUSDA+4和10.1601/nm。1462 10.1601 / strainfinder ? urlappend = % 3 fid % 3 dccbau + 05525。这些基因组中含有编码氢化酶表达的hupSLCFHK和hypBFDE基因,氢化酶是一种帮助根瘤菌吸收n2固定过程中释放的氢的酶,编码反硝化功能的napEDABC和norCBQD基因分别用于硝酸盐和一氧化氮的还原。ERR11T的基因组还含有编码氧化亚氮还原酶的nosRZDFYLX基因。基于内力基因的多位点序列分析,该新种共有8株,在10.1601/nm附近形成独特的类群。25806年分支。计算ERR11T基因组序列与近缘序列的基因组平均核苷酸同一性(Genome Average Nucleotide Identity, ANI),结果显示菌株属于10.1601/nm。25806分支(10.1601/strainfinder?)urlappend=%3Fid%3DUSDA+4和10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+15615)是与菌株ERR11T最接近的菌株,ANI为95.2%。型应变ERR11T的DDH预测值最高,为10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+15615(58.5%),其次是10.1601/strainfinder?urlappend = % 3 fid % 3 dusda + 4(53.1%)。然而,得到的ANI和DDH值在ERR11T和10.1601/strainfinder?urlappend=%3Fid%3DCCBAU+15615或10.1601/strainfinder?urlappend=%3Fid%3DUSDA+4均低于临界值(ANI≥96.5%;同一种菌株的DDH≥70%),提示ERR11T为新种。因此,基于系统发育分析、ANI和DDH值,我们正式建议创建10.1601/nm。30737 sp. 11 .带应变ERR11T (10.1601/strainfinder?urlappend = % 3 fid % 3 dhambi + 3532 T = 10.1601 / strainfinder吗?urlappend=%3Fid%3DLMG+30162 T)为型应变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Standards in Genomic Sciences
Standards in Genomic Sciences GENETICS & HEREDITY-MICROBIOLOGY
CiteScore
1.44
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0.00%
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审稿时长
6-12 weeks
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