数字农科院2.0

Identification of an Endogenous Strong Promoter in Burkholderia sp. JP2-270

文献类型: 外文期刊

作者: Jing Ke;Jiamin Shen;Haoran Wang;Xinxin Zhang;Yucong Wang;Guoqing Chen;Guozhong Feng

作者机构:

关键词: Burkholderia sp. JP2-270;overexpression;promoter;pyrrolnitrin;RNA-Seq

期刊名称: Microorganisms

ISSN: 2076-2607

年卷期: 2024 年 12 卷 9 期

页码:

收录情况: SCIE(2024版)

摘要: Burkholderia is the second largest source of natural product bacteria after Actinomyces and can produce many secondary metabolites including pyrrolnitrin (PRN). Natural products of microbial origin are usually found in trace amounts, so in metabolic engineering, promoter engineering is often used to regulate gene expression to increase yield. In this study, an endogenous strong promoter was identified based on RNA-seq to overexpress biosynthetic genes to increase the production of PRN. By analyzing the transcriptomic data of the antagonistic bacterium Burkholderia sp. JP2-270 in three different development periods, we screened 50 endogenous promoters with high transcriptional activity, nine of which were verified by an obvious fluorescent signal via fluorescence observation. Then, combined with RT-qPCR analysis, Php, the promoter of a hypothetical protein, was found to be significantly expressed in all three periods. In order to increase the suitability of endogenous promoters, the promoter Php was shortened at different lengths, and the results show that a sequence length of 173 bp was necessary for its activity. Moreover, this promoter was used to overexpress the PRN biosynthesis genes (prnA, prnB, prnC and prnD) in JP2-270, resulting in a successful increase in gene expression levels by 40–80 times. Only the overexpression of the prnB gene successfully increased PRN production to 1.46 times that of the wild type. Overall, the endogenous strong promoters screened in this study can improve gene expression and increase the production of secondary metabolites in JP2-270 and other strains.

分类号:

  • 相关文献

[1]Overexpression of the maize GRF10, an endogenous truncated growth-regulating factor protein, leads to reduction in leaf size and plant height. Wu, Lei,Xue, Ming,Qian, Jianjun,He, Yan,Wang, Shoucai,Zhang, Dengfeng. 2014

[2]EIAV基因转移载体启动子的比较. 韩凌霞,李亚明,曲连东,司昌德,姜骞,刘家森. 2006

[3]河流型水牛TGF-β基因家族鉴定及其胚胎发育早期的表达分析. 庞春英,梁莎莎,马小娅,陆杏蓉,段安琴,邓廷贤,黄韵琪,梁贤威. 2020

[4]拟南芥ago1-27突变体的RNA-seq分析. 马轩,李盛本,莫蓓莘,曹晓风,陈雪梅. 2017

[5]本生烟响应蛋白激发子PevD1的差异表达基因鉴定与分析. 梁颖博,李泽,邱德文,曾洪梅,李广悦,杨秀芬. 2019

[6]基于RNA-Seq的甘蔗主茎和分蘖茎转录组建立及初步分析. 丘立杭,罗含敏,陈荣发,黄杏,陈忠良,范业赓,陈栋,李杨瑞,吴建明. 2018

[7]基于RNA-Seq技术的o2胚乳差异表达分析. 朱慧,周志强,张东民,周昱婕,张晓星,刘红军,宋丽雅,李明顺. 2019

[8]雏鸡红细胞免疫相关基因差异表达的时序性研究. 贾悦,李月健,喻进,张晨亮,李娜娜,卢晓晓,张宁,李欣,张鼎,郝卫芳,马海利,高文伟,赵宇军,高诗敏,李建慧,李桂兰,闫芳,韩凌霞,宁官保,田文霞. 2015

[9]志贺菌耐药性与非编码RNA的关系研究. 刘翠翠,魏小娟,周绪正,李冰,牛建荣,王婧,朱阵,张继瑜. 2014

[10]应用RNA-seq数据开展鸭基因组可变剪接的鉴定与分析. 徐铁山,顾丽红,侯水生,叶保国. 2016

[11]基于RNA-Seq的稻瘟病菌Δznf1突变体的表达谱分析. 岳晓凤,阙亚伟,王政逸. 2016

[12]基于RNA-seq技术开发中间偃麦草基因组特异分子标记. 崔雨,鲍印广,王洪刚,李兴锋. 2016

[13]基因本体论在福氏志贺菌转录组研究中的应用. 朱阵,刘翠翠,王婧,张继瑜,魏小娟,周绪正,李冰,郭肖. 2014

[14]基于RNA-seq的能源植物芒转录组分析. 张贤,王建红,喻曼,曹凯,庄俐,徐昌旭,曹卫东. 2015

[15]利用RNA-Seq技术筛选不同海拔地区山羊转录组SNP. 姚娜,张文广,张兵,赵倩君,左清清,董坤哲,冯爱琴,马月辉. 2012

[16]棉花纤维发育早期RNA-Seq转录组分析. 李锡花,吴嫚,于霁雯,张金发,范术丽,宋美珍,庞朝友,喻树迅. 2013

[17]转录组测序技术的研究和应用进展. 崔凯,吴伟伟,刁其玉. 2019

[18]长链非编码RNA调控机制及其在家禽生产中的研究进展. 伊宝,姬生跃,张宏福. 2019

[19]绵羊不同发育阶段背最长肌组织中可变剪接的鉴定与分析. 鲍晶晶,浦亚斌,马月辉,赵倩君. 2019

[20]玉米穗发芽突变体vp-like8的转录组分析. 郭宇航,郑军,李润植. 2020

作者其他论文 更多>>