华北农学报 ›› 2016, Vol. 31 ›› Issue (4): 112-118. doi: 10.7668/hbnxb.2016.04.019

所属专题: 生物技术

• 论文 • 上一篇    下一篇

蛹虫草CmKexin基因克隆和菌丝体中表达检测

毛玉梅, 李琴, 付鸣佳, 金华燕, 沈俊良, 钟雪晴   

  1. 江西师范大学 生命科学学院, 江西 南昌 330022
  • 收稿日期:2016-04-26 出版日期:2016-08-28
  • 通讯作者: 付鸣佳(1964-),男,江西高安人,博士,教授,硕士生导师,主要从事食药用真菌研究。
  • 作者简介:毛玉梅(1989-),女,山东聊城人,在读硕士,主要从事食用菌分子生物学研究。
  • 基金资助:
    国家自然科学基金项目(31060004;31260010)

Clone of Gene CmKexin of Cordyceps militaris and Its Detection of Expression in Mycelium

MAO Yumei, LI Qin, FU Mingjia, JIN Huayan, SHEN Junliang, ZHONG Xueqing   

  1. College of Life Sciences, Jiangxi Normal University, Nanchang 330022, China
  • Received:2016-04-26 Published:2016-08-28

摘要: 为了探讨蛹虫草类枯草杆菌蛋白酶(Subtilisin-like protease)的表达特性,以真菌蛹虫草菌丝体为研究对象,通过RT-PCR获得蛹虫草CmKexin基因的ORF序列,并进行序列分析。应用Northern杂交和Real-time PCR方法,检测蓝光照射后蛹虫草菌丝体中CmKexin基因的转录情况。结果获得蛹虫草CmKexin基因的ORF序列。对翻译蛋白质产物CmKexin进行生物信息学分析,表明该蛋白质含1个属蛋白转化酶的肽酶S8家族功能域(143~429)和1个前体蛋白转化酶P功能域(514~600),符合真菌类枯草杆菌蛋白酶的特征。蛹虫草菌丝体在黑暗预培养4 d后再蓝光照射,Northern Blotting和Real-time PCR检测均可得到相同的结果,即在持续的蓝光照射48~50 h时,出现CmKexin基因的瞬时大量转录。而其他时间内均未检测到该基因的大量转录。试验结果将为蛹虫草类枯草杆菌蛋白酶的利用提供理论依据。

关键词: 蛹虫草, CmKexin基因, 类枯草杆菌蛋白酶, Northern杂交, 实时荧光定量PCR

Abstract: In order to study the characteristics of subtilisin-like protease expression in the mycelia of fungus Cordyceps militaris,CmKexin gene ORF sequences of C.militaris was got by RT-PCR,then CmKexin sequence was analysed.The Real-time PCR and Northern Blotting were used to the CmKexin gene expression analysis in the C.militaris mycelia in blue light irradiation of different time.Results showed the CmKexin gene ORF sequence was obtained from C.militaris mycelia.The bioinformatics analysis for the translation products of CmKexin gene showed that there were 1 peptidase S8 family domain of protein convertases (143-429) and 1 proprotein convertase P-domain(514-600) in the protein.The two domains existed in CmKexin demonstrate the characteristics of subtilisin-like protease.Under the dark pre-culture in 96 h,a large amounts of transcript of CmKexin gene in the mycelia could be detected by Northern Blotting and Real-time PCR in the continuous blue light irradiation to 48-50 hours.But the transcription of CmKexin gene wasn't detected in the other time of C.militaris mycelia culture.These results would provide the basis for using the subtilisin-like protease in Cordyceps militaris.

Key words: Cordyceps militaris, CmKexin gene, Subtilisin-like protease, Northern Blotting, Real-time PCR

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引用本文

毛玉梅, 李琴, 付鸣佳, 金华燕, 沈俊良, 钟雪晴. 蛹虫草CmKexin基因克隆和菌丝体中表达检测[J]. 华北农学报, 2016, 31(4): 112-118. doi: 10.7668/hbnxb.2016.04.019.

MAO Yumei, LI Qin, FU Mingjia, JIN Huayan, SHEN Junliang, ZHONG Xueqing. Clone of Gene CmKexin of Cordyceps militaris and Its Detection of Expression in Mycelium[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2016, 31(4): 112-118. doi: 10.7668/hbnxb.2016.04.019.

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