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海洋灰绿曲霉聚酮合酶基因的克隆与序列分析

Cloning and Functional Analysis of Fungal Polyketide Synthase Gene from Marine Aspergillus glaucus

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【作者】 李晓霞蔡孟浩胡伟李佳欣周祥山张元兴

【Author】 LI Xiao-xia;CAI Meng-hao;HU Wei;LI Jia-xin;ZHOU Xiang-shan;ZHANG Yuan-xing;State Key Laboratory of Bioreactor Engineering,School of Biotechnology,East China University of Science and Technology;

【机构】 华东理工大学生物工程学院,生物反应器工程国家重点实验室

【摘要】 为了研究海洋灰绿曲霉中抗肿瘤聚酮化合物灰绿霉素A的生物合成机制,需获得相关的聚酮合酶基因簇。根据灰绿霉素A合成途径推断,该化合物母核由非还原型PKS(NR-PKS)催化合成,本文使用LC系列简并引物得到灰绿曲霉中NR-PKS基因片段,再通过基因走读技术得到22.8kb的DNA序列,其含有7个完整的开放阅读框。通过BLAST分析,序列中包含1个NRPKS编码基因,全长8 451bp,命名为Agpks1。AgPks1与烟曲霉PksP、黑曲霉Alb1有很高的同源性。该工作对研究Agpks1对灰绿霉素A或其他聚酮产物合成的催化机制具有重要意义。

【Abstract】 It is critical to identify the polyketide synthase(PKS)gene cluster to clarify the biosynthetic mechanism of antitumor polyketide aspergiolide A,which was deduced to be catalyzed non-reduced PKS(NR-PKS)from marine Aspergillus glaucus.In this study,a NR-PKS nucleotide sequence was first obtained using the LC primers.A full sequence of its gene clusters(22.8kb)was harvested by genome walking,which contains 7ORFs by BLAST analysis.Among them,a NR-PKS gene with full length of8 451 bp was identified by BLAST and designated as Agpks1.The AgPks1 showed high homology to Aspergillus fumigatus PksP and Aspergillus niger Alb1.This work provides enlightenment for analyzing the functions of Agpks1 in biosynthetic mechanism of aspergiolide A or other polyketides produced by Aspergillus glaucus.

【基金】 国家自然科学基金(41306121,31270141);国家863计划(2011AA090702)
  • 【文献出处】 华东理工大学学报(自然科学版) ,Journal of East China University of Science and Technology(Natural Science Edition) , 编辑部邮箱 ,2014年05期
  • 【分类号】Q936
  • 【下载频次】128
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