期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
林麝肺炎克雷伯氏菌的分离鉴定及其kp05372基因的生物信息学分析 被引量:8
1
作者 赵位 王吴优 +2 位作者 程建国 田青 罗燕 《西北农林科技大学学报(自然科学版)》 CSCD 北大核心 2017年第12期23-30,共8页
【目的】对1株疑似肺炎克雷伯氏菌进行分离鉴定及全基因测序分析,并对发现的新基因kp05372编码产物进行生物信息学分析。【方法】采用传统的细菌鉴定方法和分子生物学方法,分别对采自麝粪便的1株病原菌的生理生化特征及16SrRNA序列进行... 【目的】对1株疑似肺炎克雷伯氏菌进行分离鉴定及全基因测序分析,并对发现的新基因kp05372编码产物进行生物信息学分析。【方法】采用传统的细菌鉴定方法和分子生物学方法,分别对采自麝粪便的1株病原菌的生理生化特征及16SrRNA序列进行测定;以小鼠感染试验和半数致死量(LD50)测试该病原菌的致病性;用全基因组测序方法对病原菌基因组进行测序分析,并对发现的新基因编码产物进行生物信息学分析。【结果】经生理生化试验和16SrRNA序列分析发现,分离菌株为肺炎克雷伯氏菌,命名为GPKP,其对小鼠致死的LD50为6.3×107CFU/mL。该菌基因组大小为4 879 707bp,包含5 490个开放阅读框,共注释到22组COG功能。kp05372基因编码产物由302个氨基酸组成,无信号肽,是一种不稳定的、在细胞内发挥生理作用的亲水性蛋白。【结论】分离的细菌为肺炎克雷伯氏菌,kp05372基因编码产物属于典型的LysR家族转录因子(LTTR)。 展开更多
关键词 林麝 肺炎克雷伯氏菌 kp05372 生物信息学分析
下载PDF
Preliminary study on the role of novel Lys R family gene kp05372 in Klebsiella pneumoniae of forest musk deer 被引量:3
2
作者 Wei YANG Wu-you WANG +6 位作者 Wei ZHAO Jian-guo CHENG Yin WANG Xue-ping YAO Ze-xiao YANG Dong YU Yan LUO 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2020年第2期137-154,共18页
Lys R-type transcriptional regulators are involved in the regulation of numerous cellular metabolic processes in Klebsiella pneumoniae,leading to severe infection.Earlier,we found a novel Lys R family gene,named kp053... Lys R-type transcriptional regulators are involved in the regulation of numerous cellular metabolic processes in Klebsiella pneumoniae,leading to severe infection.Earlier,we found a novel Lys R family gene,named kp05372,in a strain of K.pneumoniae(designated GPKP)isolated from forest musk deer.To study the function of this gene in relation to the biological characteristics of GPKP,we used the suicide plasmid and conjugative transfer methods to construct deletion mutant strain GPKP-Δkp05372;moreover,we also constructed the GPKP-Δkp05372+complemented strain.The role of this gene was determined by comparing the following characteristics of three strains:growth curves,biofilm formation,drug resistance,stress resistance,median lethal dose(LD50),organ colonization ability,and the histopathology of GPKP.Real-time polymerase chain reaction(RT-PCR)was used to test the expression level of seven genes upstream of kp05372.There was no significant difference in the growth rates when comparing the three bacterial strains,and no significant difference was recorded at different osmotic pressures,temperatures,salt contents,or hydrogen peroxide concentrations.The GPKP-Δkp05372 mutant formed a weak biofilm,and the other two strains formed medium biofilm.The drug resistance of the GPKP-Δkp05372 mutant toward cephalothin,cotrimoxazole,and polymyxin B was changed.The acid tolerance of the deletion strain was stronger than that of the other two strains.The LD50 values of the wild-type and complemented strains were 174-fold and 77-fold higher than that of the GPKP-Δkp05372 mutant,respectively.The colonization ability of the GPKP-Δkp05372 mutant in the heart,liver,spleen,kidney,and intestine was the weakest.The three strains caused different histopathological changes in the liver and lungs.In the GPKP-Δkp05372 mutant,the relative expression levels of kp05374 and kp05379 were increased to 1.32-fold and 1.42-fold,respectively,while the level of kp05378 was decreased by 42%.Overall,the deletion of kp05372 gene leads to changes in the following:drug resistance and acid tolerance;decreases in virulence,biofilm formation,and colonization ability of GPKP;and regulation of the upstream region of adjacent genes. 展开更多
关键词 Moschus berezovskii Klebsiella pneumoniae LysR transcription factor kp05372 gene Biological characteristics Upstream gene
原文传递
林麝源肺炎克雷伯氏菌新LysR家族转录因子的原核表达
3
作者 赵位 喻东 +3 位作者 程建国 李秋波 康纪平 罗燕 《江苏农业科学》 2020年第9期82-85,共4页
为研究林麝源肺炎克雷伯氏菌新LysR家族转录因子kp05372的功能,采用PCR方法扩增林麝源肺炎克雷伯氏菌新LysR家族转录因子kp05372基因,连接T载体进行克隆,双酶切后连接表达载体pET-32(a),构建重组表达质粒,并转入大肠杆菌BL21(DE3)细胞,... 为研究林麝源肺炎克雷伯氏菌新LysR家族转录因子kp05372的功能,采用PCR方法扩增林麝源肺炎克雷伯氏菌新LysR家族转录因子kp05372基因,连接T载体进行克隆,双酶切后连接表达载体pET-32(a),构建重组表达质粒,并转入大肠杆菌BL21(DE3)细胞,然后对其最佳表达时间、温度、IPTG浓度进行筛选,利用SDS-PAGE与Western Blot鉴定重组蛋白,得到约53.2 ku的融合蛋白,与预期大小一致。本研究成功构建kp05372基因表达载体,并筛选出最佳表达条件,为进一步研究该蛋白结构功能奠定了基础。 展开更多
关键词 林麝 肺炎克雷伯氏菌 kp05372基因 原核表达
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部