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Insect-Specific Polyketide Synthases (PKSs) Potential PKS-Nonribosomal Peptide Synthetase Hybrids and Novel PKS Clades in Tropical Fungi

机译:热带真菌中特定于昆虫的聚酮化合物合成酶(PKS)潜在的PKS-非核糖体肽合成酶杂种和新型PKS进化枝

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摘要

Polyketides draw much attention because of their potential use in pharmaceutical and biotechnological applications. This study identifies an abundant pool of polyketide synthase (PKS) genes from local isolates of tropical fungi found in Thailand in three different ecological niches: insect pathogens, marine inhabitants, and lichen mutualists. We detected 149 PKS genes from 48 fungi using PCR with PKS-specific degenerate primers. We identified and classified 283 additional PKS genes from 13 fungal genomes. Phylogenetic analysis of all these PKS sequences the comprising ketosynthase (KS) conserved region and the KS-acyltransferase interdomain region yielded results very similar to those for phylogenies of the KS domain and suggested a number of remarkable points. (i) Twelve PKS genes amplified from 12 different insect-pathogenic fungi form a tight cluster, although along with two PKS genes extracted from genomes of Aspergillus niger and Aspergillus terreus, in reducing clade III. Some of these insect-specific fungal PKSs are nearly identical. (ii) We identified 38 new PKS-nonribosomal peptide synthetase hybrid genes in reducing clade II. (iii) Four distinct clades were discovered with more than 75% bootstrap support. We propose to designate the novel clade D1 with 100% bootstrap support “reducing clade V.” The newly cloned PKS genes from these tropical fungi should provide useful and diverse genetic resources for future research on the characterization of polyketide compounds synthesized by these enzymes.
机译:聚酮化合物因其在制药和生物技术应用中的潜在用途而备受关注。这项研究从泰国的热带真菌的本地分离物中发现了丰富的聚酮化合物合酶(PKS)基因库,它们来自三种不同的生态位:昆虫病原体,海洋生物和地衣互生生物。我们使用具有PKS特异性简并引物的PCR,从48个真菌中检测到149个PKS基因。我们从13个真菌基因组中鉴定并分类了283个其他PKS基因。对所有这些酮醇合成酶(KS)保守区和KS-酰基转移酶域间区域的PKS序列进行系统进化分析,得出的结果与KS域系统发育的结果非常相似,并提出了许多显着点。 (i)从12种不同的昆虫致病真菌中扩增出的12个PKS基因形成了紧密的簇,尽管与黑曲霉和土曲霉的基因组中提取的2个PKS基因一起,在还原进化枝III中。这些昆虫特异性真菌PKS中的一些几乎相同。 (ii)我们在减少进化枝II中鉴定了38个新的PKS-非核糖体肽合成酶杂合基因。 (iii)发现了四个不同的进化枝,它们的自举支持率超过75%。我们建议指定具有100%引导程序支持的“减少V分支”的新型D1分支。从这些热带真菌中新克隆的PKS基因应为今后研究由这些酶合成的聚酮化合物的表征提供有用和多样化的遗传资源。

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