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内生链霉菌a13的鉴定、生物防治及促进植物生长潜力

Identification, Biocontrol and Plant Growth Promotion Potential of Endophytic Streptomyces sp. a13.

作者信息

Devi Chingakham Juliya, Saikia Kangkon, Mazumdar Rajkumari, Das Rictika, Bharadwaj Pranami, Thakur Debajit

机构信息

Microbial Biotechnology Laboratory, Life Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati, Assam, 781035, India.

Department of Biotechnology, Gauhati University, Guwahati, Assam, 781014, India.

出版信息

Curr Microbiol. 2025 Jan 3;82(2):64. doi: 10.1007/s00284-024-04009-9.

Abstract

Medicinal plants often harbour various endophytic actinomycetia, which are well known for their potent antimicrobial properties and plant growth-promoting traits. In this study, we isolated an endophytic actinomycetia, A13, from the leaves of tea clone P312 from the MEG Tea Estate, Meghalaya, India. The isolate A13 was identified as Streptomyces sp. A13 through whole genome sequencing (WGS) and 16S rRNA sequencing, showing 88% (ANI; Average Nucleotide Identity) and 99.78% sequence similarity with Streptomyces olivaceus. The strain A13 exhibited a prominent broad-spectrum antifungal activity against nine phytopathogens. It was observed that the ethyl acetate (EtAc) extract of A13 inhibits the spore germination rate of phytopathogen Nigrospora sphaerica (NSP) and also damages the fungal cell wall and cell structure. Additionally, the A13 strain exhibits several plant growth-promoting (PGP) traits, such as nitrogen fixation, ammonia production (4.7 µmol/ml), indole-acetic acid (IAA) production (8.91 µg/ml), siderophore production and 1-aminocyclopropane-1-carboxylate (ACC) deaminase activity Gas chromatography mass spectrometry (GC-MS) analysis revealed that Phenol, 3,5-bis(1,1-dimethylethyl) was found to be the major chemical constituent in the EtAc extract of the A13 strain, accounting for 50.15% of the area percentage. Whole genome sequencing and subsequent genome analysis utilizing bioinformatics techniques such as Antibiotics & Secondary Metabolite Analysis SHell (antiSMASH) and Rapid Annotation using Subsystem Technology (RAST) revealed a wide array of biologically active secondary metabolite biosynthesis gene clusters (smBGCs) with different physiologically significant roles. These findings emphasize the potential of the A13 strain as a biocontrol agent with the capability to enhance plant growth and prevent diseases.

摘要

药用植物常常含有各种内生放线菌,这些内生放线菌以其强大的抗菌特性和促进植物生长的特性而闻名。在本研究中,我们从印度梅加拉亚邦MEG茶园的茶树克隆品种P312的叶片中分离出一种内生放线菌A13。通过全基因组测序(WGS)和16S rRNA测序,分离株A13被鉴定为链霉菌属A13,与橄榄色链霉菌的平均核苷酸同一性(ANI)为88%,序列相似性为99.78%。菌株A13对9种植物病原菌表现出显著的广谱抗真菌活性。据观察,A13的乙酸乙酯(EtAc)提取物可抑制植物病原菌球形黑孢霉(NSP)的孢子萌发率,还会破坏真菌细胞壁和细胞结构。此外,A13菌株还表现出多种促进植物生长(PGP)的特性,如固氮、产氨(4.7微摩尔/毫升)、产吲哚 - 乙酸(IAA,8.91微克/毫升)、产铁载体以及1 - 氨基环丙烷 - 1 - 羧酸(ACC)脱氨酶活性。气相色谱 - 质谱联用(GC - MS)分析表明,苯酚,3,5 - 双(1,1 - 二甲基乙基)是A13菌株EtAc提取物中的主要化学成分,占面积百分比的50.15%。全基因组测序以及随后利用抗生素和次生代谢物分析外壳(antiSMASH)和使用子系统技术的快速注释(RAST)等生物信息学技术进行的基因组分析揭示了一系列具有不同生理重要作用的生物活性次生代谢物生物合成基因簇(smBGCs)。这些发现强调了A13菌株作为一种生物防治剂的潜力,它有能力促进植物生长并预防疾病。

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