链霉菌 UP1A-1 控制细菌枯萎病和提高茄科植物产量的基因组和功能综合分析

IF 1 Q4 GENETICS & HEREDITY
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引用次数: 0

摘要

Ralstonia solanacearum 是最具破坏性的土传病原菌之一,可导致茄科蔬菜细菌性枯萎病。从健康的茄科根瘤土壤中分离出的链霉菌 UP1A-1 表现出最低的病害发生率,并提高了茄科蔬菜的果实产量。然而,UP1A-1 的基因组和功能特性尚不清楚。因此,我们开展了本研究,通过全基因组测序来阐明 UP1A-1 的基因组特征。结果表明,链霉菌UP1A-1的基因组由8,252,902 bp组成,含有72.42%的G+C。我们确定了赋予植物生长促进(PGP)功能的基因,包括参与苷元生产、吲哚-3-乙酸生物合成、磷酸盐溶解、氮代谢和钾代谢的基因。我们还发现了几种其他基因,如几丁质酶、过氧化物酶、超氧化物歧化酶、过氧化氢酶、脯氨酸生物合成和葡萄糖脱氢酶,这些基因被认为参与了枯萎病的控制。这些基因表明,UP1A-1 菌株在生理上已适应各种环境条件,并有可能控制非生物和生物胁迫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrated genomic and functional analysis of Streptomyces sp. UP1A-1 for bacterial wilt control and solanaceae yield increase

Ralstonia solanacearum is one of the most destructive soil-borne pathogen, causing bacterial wilt to the solanaceae vegetables. Streptomyces sp. UP1A-1 isolated from healthy solanaceae rhizosphere soil, exhibited the lowest disease incidence and increased fruit yield of solanaceae vegetables. However, the genomic and functional properties of UP1A-1 are unclear. Therefore, we conducted the present study to elucidate the genomic characteristics of UP1A-1 by whole genome sequencing. The results indicate that the genome of Streptomyces sp. UP1A-1 consists of 8,252,902 bp and contains 72.42 % G + C. We identified the genes that confer plant growth promoting (PGP) function, which include those involved in siderophore production, indole-3-acetic acid biosynthesis, phosphate solubilization, nitrogen metabolism, and potassium metabolism. We also identified several other genes, such as chitinase, peroxidase, superoxide dismutase, catalase, proline biosynthesis, and glucose dehydrogenase, which are believed to be involved in the control of wilt disease. These genes revealed that the strain UP1A-1 has physiologically adapted to varied environmental conditions and could potentially control both abiotic and biotic stresses.

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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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