Heterologous gene expression and functional analysis of a type III polyketide synthase from Aspergillus niger NRRL 328

被引:7
|
作者
Kirimura, Kohtaro [1 ]
Watanabe, Shotaro [1 ]
Kobayashi, Keiichi [1 ]
机构
[1] Waseda Univ, Fac Sci & Engn, Dept Appl Chem, Shinjuku Ku, 3-4-1 Ohkubo, Tokyo 1698555, Japan
关键词
Aspergillus niger NRRL 328; Pyrone-type polyketide; Resorcinol-type polyketide; Triacetic acid lactone; Type III polyketide synthase; ACID;
D O I
10.1016/j.bbrc.2016.04.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type III polyketide synthases (PKSs) catalyze the formation of pyrone- and resorcinol-types aromatic polyketides. The genomic analysis of the filamentous fungus Aspergillus niger NRRL 328 revealed that this strain has a putative gene (chr_8_2: 2978617-2979847) encoding a type III PKS, although its functions are unknown. In this study, for functional analysis of this putative type III PKS designated as An-CsyA, cloning and heterologous expression of the An-CsyA gene (An-csyA) in Escherichia coli were performed. Recombinant His-tagged An-CsyA was successfully expressed in E. coli BL21 (DE3), purified by Ni2+-affinity chromatography, and used for in vitro assay. Tests on the substrate specificity of the His tagged An-CsyA with myriad acyl-CoAs as starter substrates and malonyl-CoA as extender substrate showed that His-tagged An-CsyA accepted fatty acyl-CoAs (C2-C14) and produced triketide pyrones (C2-C14), tetraketide pyrones (C2-C10), and pentaketide resorcinols (C10-C14). Furthermore, acetoacetyl-CoA, malonyl-CoA, isobutyryl-CoA, and benzoyl-CoA were also accepted as starter substrates, and both of triketide pyrones and tetraketide pyrones were produced. It is noteworthy that the His-tagged An-CsyA produced polyketides from malonyl-CoA as starter and extender substrates and produced tetraketide pyrones from short-chain fatty acyl-CoAs as starter substrates. Therefore, this is the first report showing the functional properties of An-CsyA different from those of other fungal type III PKSs. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1106 / 1110
页数:5
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