革兰氏阳性类芽孢杆菌(Paenibacillus sp.)的基因组和蛋白组研究
TQ458; 从西藏墨脱嘎隆拉山海拔3 000m土壤中分离出一株革兰氏阳性类芽孢杆菌(Paenibacillus sp.),用Illumi-na Hiseq测序平台进行全基因组测序以及通过Prokka1.14.6 软件进行基因组注释.结合antiSMASH 7.0 和BAGEL 4 分析Paenibacillus sp.基因组预测次级代谢产物生物合成基因簇.为了验证代谢产物路径,用不同破碎方法提取菌株全蛋白,通过蛋白质组质谱技术进行分析,结合不同蛋白质组分析软件,共鉴定了3 383 个蛋白质.通过同源比对,提取的蛋白质中可以检测到套索肽生物合成基因簇中依赖ATP半胱氨酸蛋白酶N端区域B1 和A...
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Published in | 应用化工 Vol. 53; no. 4; pp. 797 - 801 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Chinese |
Published |
中国科学院青藏研究所青藏高原地球系统与资源环境重点实验室,北京 100101%兰州大学 生态学院,甘肃 兰州 730000%兰州大学 泛第三极环境中心,甘肃 兰州 730000%北京工业大学科学技术发展院,北京 100101
2024
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Subjects | |
Online Access | Get full text |
ISSN | 1671-3206 |
DOI | 10.3969/j.issn.1671-3206.2024.04.010 |
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Abstract | TQ458; 从西藏墨脱嘎隆拉山海拔3 000m土壤中分离出一株革兰氏阳性类芽孢杆菌(Paenibacillus sp.),用Illumi-na Hiseq测序平台进行全基因组测序以及通过Prokka1.14.6 软件进行基因组注释.结合antiSMASH 7.0 和BAGEL 4 分析Paenibacillus sp.基因组预测次级代谢产物生物合成基因簇.为了验证代谢产物路径,用不同破碎方法提取菌株全蛋白,通过蛋白质组质谱技术进行分析,结合不同蛋白质组分析软件,共鉴定了3 383 个蛋白质.通过同源比对,提取的蛋白质中可以检测到套索肽生物合成基因簇中依赖ATP半胱氨酸蛋白酶N端区域B1 和ABC转运器.同时,用BAGEL4 软件blastp功能从NCBI数据库中获取Paenibacillus sp.基因组中潜在完整的套索肽生物合成基因簇. |
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AbstractList | TQ458; 从西藏墨脱嘎隆拉山海拔3 000m土壤中分离出一株革兰氏阳性类芽孢杆菌(Paenibacillus sp.),用Illumi-na Hiseq测序平台进行全基因组测序以及通过Prokka1.14.6 软件进行基因组注释.结合antiSMASH 7.0 和BAGEL 4 分析Paenibacillus sp.基因组预测次级代谢产物生物合成基因簇.为了验证代谢产物路径,用不同破碎方法提取菌株全蛋白,通过蛋白质组质谱技术进行分析,结合不同蛋白质组分析软件,共鉴定了3 383 个蛋白质.通过同源比对,提取的蛋白质中可以检测到套索肽生物合成基因簇中依赖ATP半胱氨酸蛋白酶N端区域B1 和ABC转运器.同时,用BAGEL4 软件blastp功能从NCBI数据库中获取Paenibacillus sp.基因组中潜在完整的套索肽生物合成基因簇. |
Abstract_FL | It isolated a Gram positive Paenibacillus sp.strain from the soil at an altitude of 3 000 m in the Kalongla Mountains in Mutuo,Tibet.The entire genome of Paenibacillus sp.strain was sequenced by Illu-mina Hiseq and was annotated with Prokka software(v1.14.6).antiSMASH 7.0 and BAGEL4 were used to predict the secondary metabolites biosynthesis gene cluster in Paenibacillus sp.In order to validate the metabolic pathway,the total strain proteins were extracted by various extraction methods and performed nanoliter liquid chromatography combining with Mass Spectrometry.We could identify a total of 3 383 pro-teins by using software.Through homologous comparison,there were the N-terminal region of ATP depend-ent Cysteine protease B1 and ABC transporter in the lasso peptide biosynthesis gene cluster.It was com-plete by local blast comparison,and Paenibacillus sp.was likely to have the ability to synthesize lasso pep-tide.Through the above research,we analyed genomic and proteomic information of Paenibacillus sp. |
Author | 杨小琴 张蕾 张雪 计慕侃 宋丽丽 张更新 |
AuthorAffiliation | 中国科学院青藏研究所青藏高原地球系统与资源环境重点实验室,北京 100101%兰州大学 生态学院,甘肃 兰州 730000%兰州大学 泛第三极环境中心,甘肃 兰州 730000%北京工业大学科学技术发展院,北京 100101 |
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Author_FL | ZHANG Geng-xin JI Mu-kan YANG Xiao-qin ZHANG Lei SONG Li-li ZHANG Xue |
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DocumentTitle_FL | Genome and proteome analysis of Paenibacillus sp |
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Keywords | genome secondary metabolites 基因簇 Paenibacillus 次级代谢产物 蛋白质组 基因组 gene cluster 类芽孢杆菌 proteome |
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Snippet | TQ458; 从西藏墨脱嘎隆拉山海拔3 000m土壤中分离出一株革兰氏阳性类芽孢杆菌(Paenibacillus sp.),用Illumi-na Hiseq测序平台进行全基因组测序以及通过Prokka1.14.6 软件进行基因组注释.结合antiSMASH 7.0 和BAGEL 4 分析Paenibacillus... |
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Title | 革兰氏阳性类芽孢杆菌(Paenibacillus sp.)的基因组和蛋白组研究 |
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