[1]张岩,伍辉军,周晓辉,等.丁香假单胞大豆致病变种harpin编码基因的克隆表达与功能研究[J].南京农业大学学报,2013,36(1):6-12.[doi:10.7685/j.issn.1000-2030.2013.01.002]
 ZHANG Yan,WU Huijun,ZHOU Xiaohui,et al.Cloning,expressing and function of a harpin-encoding gene from Pseudomonas syringae pv. glycinea[J].Journal of Nanjing Agricultural University,2013,36(1):6-12.[doi:10.7685/j.issn.1000-2030.2013.01.002]
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丁香假单胞大豆致病变种harpin编码基因的克隆表达与功能研究()
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《南京农业大学学报》[ISSN:1000-2030/CN:32-1148/S]

卷:
36卷
期数:
2013年1期
页码:
6-12
栏目:
出版日期:
2013-01-24

文章信息/Info

Title:
Cloning,expressing and function of a harpin-encoding gene from Pseudomonas syringae pv. glycinea
作者:
张岩 伍辉军 周晓辉 高学文
南京农业大学植物保护学院/农作物生物灾害综合治理教育部重点实验室, 江苏 南京 210095
Author(s):
ZHANG Yan WU Huijun ZHOU Xiaohui GAO Xuewen
College of Plant Protection/Key Laboratory of Integrated Management of Crop Diseases and Pests, Ministry of Education, Nanjing Agricultural University, Nanjing 210095, China
关键词:
丁香假单胞大豆致病变种harpin编码基因GST融合表达烟草过敏性反应促生
Keywords:
Pseudomonas syringae pv. glycineaharpin-encoding geneGST fusion expressiontobaccohypersensitive responsegrowth promotion
分类号:
S432.42
DOI:
10.7685/j.issn.1000-2030.2013.01.002
摘要:
采用PCR方法从丁香假单胞大豆致病变种(Pseudomonas syringae pv.glycinea)A1和S1菌株中分别克隆到大小为1 026和1 038 bp的hrpZ基因(hrpZPsgA11和hrpZPsgS11),对该基因进行了原核表达和功能研究。SDS-PAGE显示其表达产物为相对分子质量62×103的融合蛋白,harpinZPsgA1和harpinZPsgS1的相对分子质量约为35×103。harpinZPsgS1的粗提蛋白经GSTrap FF纯化后质量浓度可达1.1 mg·mL-1。生物活性检测表明,该蛋白对热稳定,对蛋白酶K敏感,可以在非寄主植物烟草上激发过敏反应,过敏反应可以被真核生物代谢抑制剂抑制,并且对烟草有明显的促生作用。序列比对发现,来自丁香假单胞大豆致病变种的hrpZ基因可分为2类,一类以hrpZPsgA1为代表,包括hrpZPsg12,另一类以hrpZPsgS1为代表,包括来自r0和Race4菌株的hrpZ基因。这2类hrpZ基因的核苷酸同源性为79%,氨基酸同源性为77%,均富含甘氨酸,不含半胱氨酸,与假单胞菌属以外的其他革兰氏阴性植物病原细菌harpin编码基因不存在相似性。
Abstract:
We amplified the hrpZ(hypersensitive response and pathogenicity)genes from Pseudomonas syringae pv.glycinea isolates A1 and S1 genomic DNA by PCR technique,named hrpZPsgA11 and hrpZPsgS11,and the size were 1 026 bp and 1 038 bp.The fusion harpin protein was expressed in Escherichia coli BL21 and purified by GSTrap FF.The SDS-PAGE gel showed that fusion protein was 62×103,and the molecular mass of harpinZPsgA1 and harpinZPsgS1 were 35×103.The concentration of pure harpinZPsgS1 was 1.1 mg·mL-1.Bioassay results showed that the protein was heat-stable and protein K sensitive,and was able to trigger hypersensitive response(HR)in common tobacco.Besides,the HR elicitation of the protein in tobacco was dispelled by eukayotic metabolic inhibitors.Moreover,it could promote tobacco growth.Sequence alignment showed that hrpZ of Pseudomonas syringae pv. glycinea could be divided into two categories:a class with hrpZPsgA11 as representative,including hrpZPsg1212,the other class with hrpZPsgS11 as representative,including the hrpZ genes from the strains of r0 and Race4.The nucleotide homology of these two classes was 79% and the protein homology was 77%,which contained abundant glycine(G),but had no cysteine(C).However,it did not show any sequence identity with those of other genus of gram-negative plant pathogenic bacteria.This study provides genetic resources for research and development of new microbial protein pesticides and for disease and pest resistance genetic engineering.

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相似文献/References:

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 ZHANG Yang,WU Huijun,ZHANG Hongyue,et al.Functional identification of the differential regions of HrpZ protein from Pseudomonas syringae pv.glycinea[J].Journal of Nanjing Agricultural University,2016,39(1):89.[doi:10.7685/jnau.201503020]

备注/Memo

备注/Memo:
收稿日期:2012-3-12。
作者简介:张岩,硕士研究生。
通讯作者:高学文,教授,博导,研究方向为分子植物病理学和植物病害生物防治, E-mail:gaoxw@njau.edu.cn。
更新日期/Last Update: 1900-01-01