首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >A polyketide synthase-peptide synthetase gene cluster from an uncultured bacterial symbiont of Paederus beetles
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A polyketide synthase-peptide synthetase gene cluster from an uncultured bacterial symbiont of Paederus beetles

机译:Pa甲未培养细菌共生体中的聚酮合酶-肽合成酶基因簇

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摘要

Many drug candidates from marine and terrestrial invertebrates are suspected metabolites of uncultured bacterial symbionts. The antitumor polyketides of the pederin family, isolated from beetles and sponges, are an example. Drug development from such sources is commonly hampered by low yields and the difficulty of sustaining invertebrate cultures. To obtain insight into the true producer and find alternative supplies of these rare drug candidates, the putative pederin biosynthesis genes were cloned from total DNA of Paederus fuscipes beetles, which use this compound for chemical defense. Sequence analysis of the gene cluster and adjacent regions revealed the presence of ORFs with typical bacterial architecture and homologies. The ped cluster, which is present only in beetle specimens with high pederin content, is located on a 54-kb region bordered by transposase pseudogenes and encodes a mixed modular polyketide synthaseonribosomal peptide synthetase. Notably, none of the modules contains regions with homology to acyltransferase domains, but two copies of isolated monodomain acyltransferase genes were found at the upstream end of the cluster. In line with an involvement in pederin biosynthesis, the upstream cluster region perfectly mirrors pederin structure. The unexpected presence of additional polyketide synthaseonribosomal peptide synthetase modules reveals surprising insights into the evolutionary relationship between pederin-type pathways in beetles and sponges.
机译:来自海洋和陆地无脊椎动物的许多候选药物被怀疑是未经培养的细菌共生体的代谢产物。从甲虫和海绵中分离出来的pederin家族的抗肿瘤聚酮化合物就是一个例子。这种来源的药物开发通常因产量低和维持无脊椎动物培养的困难而受到阻碍。为了深入了解真正的生产者并寻找这些稀有药物的替代供应品,从Paederus fuscipes甲虫的总DNA中克隆了假定的pederin生物合成基因,并将其用于化学防御。基因簇和相邻区域的序列分析表明存在具有典型细菌结构和同源性的ORF。 ped簇仅存在于具有较高pederin含量的甲虫标本中,位于转座酶假基因接壤的54 kb区域,并编码混合的模块化聚酮化合物合酶/非核糖体肽合成酶。值得注意的是,没有一个模块包含与酰基转移酶结构域同源的区域,但是在簇的上游末端发现了两个拷贝的分离的单结构域酰基转移酶基因。与参与pederin的生物合成相一致,上游簇区域完美地反映了pederin的结构。其他聚酮化合物合酶/非核糖体肽合成酶模块的意外出现揭示了甲虫和海绵中pederin-型途径之间进化关系的令人惊讶的见解。

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