Department of Microbiology, Chong Qing Medica University, 400016 Chongqing, People's Republic of China.
Mol Biol Rep. 2009 Nov;36(8):2291-7. doi: 10.1007/s11033-009-9447-0. Epub 2009 Jan 17.
Fatty acid composition of fungi is analysed through the gas chromatography technique. With specific activity a novel enzyme Delta6-fatty acid desaturase was screened and isolated from Rhizopus nigricans. In this study R. nigricans was identified as a fungal species that produced plentiful gamma-linolenic acid. A 1,475 bp full-length cDNA, designated as RnD6D here, with high homology to fungal Delta6-fatty acid desaturase genes was isolated from R. nigricans using reverse transcription polymerase chain reaction and rapid amplification of cDNA ends methods. Sequence analysis indicated that this cDNA sequence had an open reading frame of 1,380 bp encoding a deduced polypeptide of 459 amino acids. Bioinformatics analysis characterized the putative RnD6D protein as a typical membrane-bound desaturase, including three conserved histidine-rich motifs, hydropathy profile and a cytochrome b5-like domain in the N-terminus. The corresponding genomic sequence of RnD6D was 1,689 bp with 4 introns, which was at least one intron more than other fungal Delta6-fatty acid desaturase genes. To elucidate the function of this novel putative desaturase, the coding sequence was expressed in Saccharomyces cerevisiae strain INVScl. A novel peak corresponding to gamma-linolenic acid methyl ester standards was detected with the same retention time, which was absent in the cell transformed with empty vector. The result demonstrated that the coding produced Delta6-fatty acid desaturase activity of RnD6D which led to the accumulation of gamma-linolenic acid. The functionally active RnD6D gene cloned here defined a novel Delta6-fatty acid desaturase from R. nigricans.
真菌的脂肪酸组成通过气相色谱技术进行分析。通过特异性活性,从黑根霉中筛选并分离出一种新型酶Δ6-脂肪酸去饱和酶。在这项研究中,黑根霉被鉴定为一种产生大量γ-亚麻酸的真菌。从黑根霉中使用反转录聚合酶链反应和快速扩增 cDNA 末端方法分离出一个全长 1475bp 的 cDNA,命名为 RnD6D,与真菌Δ6-脂肪酸去饱和酶基因具有高度同源性。序列分析表明,该 cDNA 序列具有 1380bp 的开放阅读框,编码一个 459 个氨基酸的推定多肽。生物信息学分析将推定的 RnD6D 蛋白特征化为典型的膜结合去饱和酶,包括三个保守的富含组氨酸的基序、疏水性图谱和 N 端的细胞色素 b5 样结构域。RnD6D 的相应基因组序列为 1689bp,有 4 个内含子,比其他真菌Δ6-脂肪酸去饱和酶基因至少多一个内含子。为了阐明这种新型推定去饱和酶的功能,将编码序列在酿酒酵母 INVScl 菌株中表达。检测到一个与γ-亚麻酸甲酯标准品相同保留时间的新峰,而在转化为空载体的细胞中则没有。结果表明,该编码产生了 RnD6D 的Δ6-脂肪酸去饱和酶活性,导致γ-亚麻酸的积累。这里克隆的具有功能活性的 RnD6D 基因定义了一种来自黑根霉的新型Δ6-脂肪酸去饱和酶。