华北农学报 ›› 2009, Vol. 24 ›› Issue (5): 35-39. doi: 10.7668/hbnxb.2009.05.008

• 论文 • 上一篇    下一篇

哈茨木霉厚垣孢子产生突变体的筛选及T-DNA标签序列的克隆

黄亚丽1,2, 蒋细良3, 田云龙2, 朱昌雄2   

  1. 1. 河北省生物研究所, 河北石家庄 050081;
    2. 中国农业科学院环发所, 北京 100081;
    3. 中国农业科学院植物保护研究所, 植物病虫害生物学国家重点实验室, 北京 100094
  • 收稿日期:2009-07-04 出版日期:2009-10-28
  • 通讯作者: 朱昌雄(1963-),男,福建福安人,博士,研究员,博士生导师,主要从事生物防治研究。
  • 作者简介:黄亚丽(1975-),女,河北肃宁人,副研究员,博士,主要从事植物病害的生物防治研究。
  • 基金资助:
    国家自然科学基金项目(30671400);“十一五”支撑项目(2006BAD08A02);“863”项目(2006AA10A211)

Study on Screening of Chlamydospore Formation Mutants from T-DNA Insertional Mutant Library of Trichoderma harzianum and Cloning of T-DNA Tagging Sequence

HUANG Ya-li1,2, JIANG Xi-liang3, TIAN Yun-long2, ZHU Chang-xiong2   

  1. 1. Biological Institute of Hebei Province, Shijiazhuang 050081, China;
    2. Institute of Agricultural Environment and Sustainable Development, Chinese Academy of Agricalture Sciences, Beijing 100081, China;
    3. State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricalture Sciences, Beijing 100094, China
  • Received:2009-07-04 Published:2009-10-28

摘要: 利用PD液体培养基从哈茨木霉T-DNA插入突变体库中筛选出在产孢性状上与野生型菌株明显不同突变子7株,其突变表型主要表现在分生孢子产生数量显著减少和菌丝上有大量厚垣孢子分化。利用TAIL-PCR方法对7株突变体的侧翼序列进行克隆,从5个突变体中获取了5条T-DNA侧翼序列。为木霉菌厚垣孢子产生相关全长基因的克隆和产孢机制的研究奠定了基础。

关键词: 哈茨木霉, T-DNA, 突变子, TAIL-PCR, 厚垣孢子

Abstract: 7 mutants with chlamydospore format ion differences were selected from 1 192 transformants cultured in PD liquid medium.The conidia formation ability of all these 7 mutants was signif icantly lower than that of the wild type T.harzianum.The characterization of these 7 mutants was analyzed.The results showed that as for the mutants 918,1137,1317 chlamydospore developed in the mycelium and falled off from mycelium when incubated time prolonged.However,as for the other 4 mutants 627,840,1137,1173 the chlamydospore couldn't falled off from mycelium when incubated time prolonged.Using TAIL-PCR to clone T-DNA right border sequences from spore formation mutants,we successfully obtained the fungal genomic DNA sequences flanking T-DNA right border from 5 transformants.The homologous sequences of 3 sequences were found by using Blastn and Blastx from NCBI GenBank.However,the homologous sequences of other 2 sequences were not found.They might be new genes related to spore formation which need to be further studied.This study is the base for the cloning of chlamydospore related gene and the mechanism research of chlamydospore formation.

Key words: Trichoderma harzianum, T-DNA, Mutant, TAIL-PCR, Chlamydospore

中图分类号: 

引用本文

黄亚丽, 蒋细良, 田云龙, 朱昌雄. 哈茨木霉厚垣孢子产生突变体的筛选及T-DNA标签序列的克隆[J]. 华北农学报, 2009, 24(5): 35-39. doi: 10.7668/hbnxb.2009.05.008.

HUANG Ya-li, JIANG Xi-liang, TIAN Yun-long, ZHU Chang-xiong. Study on Screening of Chlamydospore Formation Mutants from T-DNA Insertional Mutant Library of Trichoderma harzianum and Cloning of T-DNA Tagging Sequence[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2009, 24(5): 35-39. doi: 10.7668/hbnxb.2009.05.008.

使用本文

0
    /   /   推荐 /   导出引用

链接本文: http://www.hbnxb.net/CN/10.7668/hbnxb.2009.05.008

               http://www.hbnxb.net/CN/Y2009/V24/I5/35