中国医药生物技术
中國醫藥生物技術
중국의약생물기술
CHINESE MEDICINAL BIOTECHNOLOGY
2015年
4期
330-334
,共5页
朱丽%饶敏%蒋美珍%戈梅
硃麗%饒敏%蔣美珍%戈梅
주려%요민%장미진%과매
东方拟无枝酸菌%ECO-0501%AORI_2943
東方擬無枝痠菌%ECO-0501%AORI_2943
동방의무지산균%ECO-0501%AORI_2943
Amycolatopsis orientalis%ECO-0501%AORI_2943
目的 对位于ECO-0501生物合成基因簇内AORI_2943基因进行功能鉴定,进一步解析东方拟无枝酸菌中ECO-0501的生物合成途径.方法 通过同源重组和定点整合的方式构建AORI_2943缺失、回补及过表达突变株.高效液相及质谱分析突变株发酵产物的变化,分析AORI_2943在 ECO-0501合成中的作用.结果 AORI_2943缺失突变株不产ECO-0501和去甲基ECO-0501,只产生结构上缺失了C5N单位(2-氨基-3-羟基环戊-2-烯酮)的前体物质a和b,发酵液中未检测出C5N单位.对缺失突变株回补后,有少量ECO-0501及去甲基ECO-0501产生,同时仍然有大量前体化合物a和b的积累.在野生菌的基础上过表达AORI_2943,并未明显提高ECO-0501的产量.结论 AORI_2943是ECO-0501合成的关键基因,主要参与了ECO-0501前体化合物 C5N单位的合成.
目的 對位于ECO-0501生物閤成基因簇內AORI_2943基因進行功能鑒定,進一步解析東方擬無枝痠菌中ECO-0501的生物閤成途徑.方法 通過同源重組和定點整閤的方式構建AORI_2943缺失、迴補及過錶達突變株.高效液相及質譜分析突變株髮酵產物的變化,分析AORI_2943在 ECO-0501閤成中的作用.結果 AORI_2943缺失突變株不產ECO-0501和去甲基ECO-0501,隻產生結構上缺失瞭C5N單位(2-氨基-3-羥基環戊-2-烯酮)的前體物質a和b,髮酵液中未檢測齣C5N單位.對缺失突變株迴補後,有少量ECO-0501及去甲基ECO-0501產生,同時仍然有大量前體化閤物a和b的積纍.在野生菌的基礎上過錶達AORI_2943,併未明顯提高ECO-0501的產量.結論 AORI_2943是ECO-0501閤成的關鍵基因,主要參與瞭ECO-0501前體化閤物 C5N單位的閤成.
목적 대위우ECO-0501생물합성기인족내AORI_2943기인진행공능감정,진일보해석동방의무지산균중ECO-0501적생물합성도경.방법 통과동원중조화정점정합적방식구건AORI_2943결실、회보급과표체돌변주.고효액상급질보분석돌변주발효산물적변화,분석AORI_2943재 ECO-0501합성중적작용.결과 AORI_2943결실돌변주불산ECO-0501화거갑기ECO-0501,지산생결구상결실료C5N단위(2-안기-3-간기배무-2-희동)적전체물질a화b,발효액중미검측출C5N단위.대결실돌변주회보후,유소량ECO-0501급거갑기ECO-0501산생,동시잉연유대량전체화합물a화b적적루.재야생균적기출상과표체AORI_2943,병미명현제고ECO-0501적산량.결론 AORI_2943시ECO-0501합성적관건기인,주요삼여료ECO-0501전체화합물 C5N단위적합성.
Objective To determine the function of theAORI_2943gene located in the biosynthesis gene cluster of ECO-0501 from Amycolatopsis orientalis. Methods The disruption, complementation and overexpression ofAORI_2943 were conducted by homologous recombination and site-specified integration. The metabolites in the fermentation broth of the resulted mutants were analyzed by high performance liquid chromatography and mass spectrometry. Results Disruption ofAORI_2943 inAmycolatopsis orientalis resulted in the disappearance of ECO-0501 and demethyl-ECO-0501 and the appearance of two new compounds a and b in the fermentation broth of the mutant. The two new compounds a and b, lacking the 2-amino-3-hydroxy-cyclopent-2-enone moiety (C5N) in ECO-0501, were determined as the precursors of ECO-0501 and demethyl-ECO-0501, respectively. Complementation of the disrupted mutant with intactAORI_2943 restored the ECO-0501 production. However, overexpression ofAORI_2943 did not improve the production of ECO-0501. ConclusionAORI_2943 is crucial for ECO-0501, specifically the C5N unit biosynthesis. To improve the production of ECO-0501, overexpression ofAORI_2943 alone is not enough.