Bhattacharyya Chandrima, Bakshi Utpal, Mallick Ivy, Mukherji Shayantan, Bera Biswajit, Ghosh Abhrajyoti
Department of Biochemistry, Bose Institute Kolkata, India.
Structural Biology and Bioinformatics Division, CSIR - Indian Institute of Chemical BiologyKolkata, India; Tea Board of India, Ministry of Commerce and IndustryKolkata, India.
Front Microbiol. 2017 Mar 21;8:411. doi: 10.3389/fmicb.2017.00411. eCollection 2017.
AB211 is a plant growth promoting, Gram-positive firmicute, isolated from the rhizosphere of tea (), one of the oldest perennial crops and a major non-alcoholic beverage widely consumed all over the world. The whole genome of AB211 was sequenced, annotated and evaluated with special focus on genomic elements related to plant microbe interaction. It's genome sequence reveals the presence of a 5,403,026 bp chromosome. A total of 5226 putative protein-coding sequences, 16 rRNA, 120 tRNA, 8 ncRNAs, 58 non-protein coding genes, and 11 prophage regions were identified. Genome sequence comparisons between strain AB211 and other related environmental strains of , identified about 3558 genes conserved among all genomes analyzed. Most of the common genes involved in plant growth promotion activities were found to be present within core genes of all the genomes used for comparison, illustrating possible common plant growth promoting traits shared among all the strains of . Besides the core genes, some genes were exclusively identified in the genome of strain AB211. Functional annotation of the genes predicted in the strain AB211 revealed the presence of genes responsible for mineral phosphate solubilization, siderophores, acetoin, butanediol, exopolysaccharides, flagella biosynthesis, surface attachment/biofilm formation, and indole acetic acid production, most of which were experimentally verified in the present study. Genome analysis and experimental evidence suggested that AB211 has robust central carbohydrate metabolism implying that this bacterium can efficiently utilize the root exudates and other organic materials as an energy source. Genes for the production of peroxidases, catalases, and superoxide dismutases, that confer resistance to oxidative stresses in plants were identified in AB211 genome. Besides these, genes for heat shock tolerance, cold shock tolerance, glycine-betaine production, and antibiotic/heavy metal resistance that enable bacteria to survive biotic/abiotic stress were also identified. Based on the genome sequence information and experimental evidence as presented in this study, strain AB211 appears to be metabolically diverse and exhibits tremendous potential as a plant growth promoting bacterium.
AB211是一种促进植物生长的革兰氏阳性厚壁菌,从茶树根际分离得到。茶树是最古老的多年生作物之一,也是全世界广泛消费的一种主要非酒精饮料。对AB211的全基因组进行了测序、注释和评估,特别关注与植物-微生物相互作用相关的基因组元件。其基因组序列显示存在一条5403026 bp的染色体。共鉴定出5226个推定的蛋白质编码序列、16个rRNA、120个tRNA、8个非编码RNA、58个非蛋白质编码基因和11个原噬菌体区域。通过对AB211菌株与其他相关环境菌株的基因组序列比较,在所有分析的基因组中鉴定出约3558个保守基因。发现大多数参与植物生长促进活动的常见基因存在于用于比较的所有基因组的核心基因中,这说明所有菌株可能具有共同的促进植物生长的特性。除了核心基因外,还在AB211菌株的基因组中专门鉴定出一些基因。对AB211菌株中预测的基因进行功能注释,发现存在负责矿物磷酸盐溶解、铁载体、3-羟基丁酮、丁二醇、胞外多糖、鞭毛生物合成、表面附着/生物膜形成和吲哚乙酸产生的基因,其中大多数在本研究中得到了实验验证。基因组分析和实验证据表明,AB211具有强大的中心碳水化合物代谢能力,这意味着该细菌可以有效地利用根系分泌物和其他有机物质作为能源。在AB211基因组中鉴定出了赋予植物抗氧化应激能力的过氧化物酶、过氧化氢酶和超氧化物歧化酶的基因。除此之外,还鉴定出了使细菌能够在生物/非生物胁迫下存活的耐热、耐冷、甘氨酸甜菜碱产生以及抗生素/重金属抗性的基因。基于本研究中提供的基因组序列信息和实验证据,AB211菌株似乎具有多样的代谢能力,作为一种促进植物生长的细菌具有巨大潜力。