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嗜盐ASH15的基因组分析揭示了其对盐的适应性、促进植物生长的特性以及类异戊二烯生物合成机制。

Genome analysis of a halophilic ASH15 revealed salt adaptation, plant growth promotion, and isoprenoid biosynthetic machinery.

作者信息

Sharma Anjney, Singh Ram Nageena, Song Xiu-Peng, Singh Rajesh Kumar, Guo Dao-Jun, Singh Pratiksha, Verma Krishan K, Li Yang-Rui

机构信息

Key Laboratory of Sugarcane Biotechnology and Genetic Improvement, Ministry of Agriculture, Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Guangxi Academy of Agricultural Sciences (GXXAS), Nanning, Guangxi, China.

Guangxi Key Laboratory of Sugarcane Genetic Improvement, Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.

出版信息

Front Microbiol. 2023 Sep 22;14:1229955. doi: 10.3389/fmicb.2023.1229955. eCollection 2023.

Abstract

Globally, due to widespread dispersion, intraspecific diversity, and crucial ecological components of halophilic ecosystems, bacteria is considered one of the key models for ecological, adaptative, and biotechnological applications research in saline environments. With this aim, the present study was to enlighten the plant growth-promoting features and investigate the systematic genome of a halophilic bacteria, ASH15, through single-molecule real-time (SMRT) sequencing technology. Results showed that strain ASH15 could survive in high salinity up to 25% (w/v) NaCl concentration and express plant growth-promoting traits such as nitrogen fixation, plant growth hormones, and hydrolytic enzymes, which sustain salt stress. The results of pot experiment revealed that strain ASH15 significantly enhanced sugarcane plant growth (root shoot length and weight) under salt stress conditions. Moreover, the sequencing analysis of the strain ASH15 genome exhibited that this strain contained a circular chromosome of 3,832,903 bp with an average G+C content of 37.54%: 3721 predicted protein-coding sequences (CDSs), 24 rRNA genes, and 62 tRNA genes. Genome analysis revealed that the genes related to the synthesis and transport of compatible solutes (glycine, betaine, ectoine, hydroxyectoine, and glutamate) confirm salt stress as well as heavy metal resistance. Furthermore, functional annotation showed that the strain ASH15 encodes genes for root colonization, biofilm formation, phytohormone IAA production, nitrogen fixation, phosphate metabolism, and siderophore production, which are beneficial for plant growth promotion. Strain ASH15 also has a gene resistance to antibiotics and pathogens. In addition, analysis also revealed that the genome strain ASH15 has insertion sequences and CRISPRs, which suggest its ability to acquire new genes through horizontal gene transfer and acquire immunity to the attack of viruses. This work provides knowledge of the mechanism through which ASH15 tolerates salt stress. Deep genome analysis, identified MVA pathway involved in biosynthesis of isoprenoids, more precisely "Squalene." Squalene has various applications, such as an antioxidant, anti-cancer agent, anti-aging agent, hemopreventive agent, anti-bacterial agent, adjuvant for vaccines and drug carriers, and detoxifier. Our findings indicated that strain ASH15 has enormous potential in industries such as in agriculture, pharmaceuticals, cosmetics, and food.

摘要

在全球范围内,由于嗜盐生态系统分布广泛、种内多样性以及关键的生态组成部分,细菌被认为是盐环境中生态、适应性和生物技术应用研究的关键模型之一。出于这个目的,本研究旨在通过单分子实时(SMRT)测序技术,揭示一种嗜盐细菌ASH15促进植物生长的特性,并研究其系统基因组。结果表明,菌株ASH15能够在高达25%(w/v)NaCl浓度的高盐环境中存活,并表现出促进植物生长的特性,如固氮、植物生长激素和水解酶,这些特性有助于维持盐胁迫。盆栽试验结果表明,菌株ASH15在盐胁迫条件下显著促进了甘蔗植株的生长(根和茎的长度及重量)。此外,对菌株ASH15基因组的测序分析表明,该菌株含有一个3,832,903 bp的环状染色体,平均G+C含量为37.54%:3721个预测的蛋白质编码序列(CDS)、24个rRNA基因和62个tRNA基因。基因组分析表明,与相容性溶质(甘氨酸、甜菜碱、四氢嘧啶、羟基四氢嘧啶和谷氨酸)合成和运输相关的基因证实了其对盐胁迫以及重金属的抗性。此外,功能注释表明,菌株ASH15编码与根部定殖、生物膜形成、植物激素IAA产生、固氮、磷代谢和铁载体产生相关的基因,这些基因有利于促进植物生长。菌株ASH15还具有对抗生素和病原体的抗性基因。此外,分析还表明,基因组菌株ASH15具有插入序列和CRISPRs,这表明其能够通过水平基因转移获得新基因,并获得对病毒攻击的免疫力。这项工作提供了关于ASH15耐受盐胁迫机制的知识。深入的基因组分析确定了参与类异戊二烯生物合成的MVA途径,更确切地说是“角鲨烯”。角鲨烯有多种应用,如抗氧化剂、抗癌剂、抗衰老剂、止血剂、抗菌剂、疫苗佐剂和药物载体以及解毒剂。我们的研究结果表明,菌株ASH15在农业、制药、化妆品和食品等行业具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e653/10556750/affe07f29404/fmicb-14-1229955-g0001.jpg

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