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从甘露糖赤藓糖醇脂B非对映异构体型生产者筑波假丝酵母中鉴定编码乙酰转移酶的基因PtMAT1

Identification of the gene PtMAT1 encoding acetyltransferase from the diastereomer type of mannosylerythritol lipid-B producer Pseudozyma tsukubaensis.

作者信息

Saika Azusa, Utashima Yu, Koike Hideaki, Yamamoto Shuhei, Kishimoto Takahide, Fukuoka Tokuma, Morita Tomotake

机构信息

Research Institute for Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 5-2, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan.

Toyobo Co., Ltd., Tsuruga Institute of Biotechnology, 10-24 Toyo-cho, Tsuruga, Fukui 914-8550, Japan.

出版信息

J Biosci Bioeng. 2018 Dec;126(6):676-681. doi: 10.1016/j.jbiosc.2018.05.025. Epub 2018 Jul 20.

Abstract

Mannosylerythritol lipids (MELs) are biosurfactants produced from feedstocks by basidiomycetous yeasts. MELs exhibit different properties depending on their structures, such as the degree of acetylation or acylation and the chirality of the mannosylerythritol moiety. Pseudozyma tsukubaensis produces a diastereomer type of MEL-B (mono-acetylated MEL); therefore, deletion of an acetyltransferase could yield a diastereomer type of MEL-D (deacetylated MEL), which has only been produced in in vitro reactions of lipase using MEL-B as a substrate. Here, we deleted the gene PtMAT1 in P. tsukubaensis 1E5 encoding an acetyltransferase related to MEL biosynthesis via targeted gene deletion and generated a producer of the diastereomer type of MEL-D. The uracil auxotrophic mutant of P. tsukubaensis 1E5 (PtURA5-mutant) was used as a host strain for gene deletion. The gene PtMAT1 was replaced with a PtURA5 cassette by homologous recombination using uracil auxotrophy as a selectable marker. According to thin-layer chromatography and nuclear magnetic resonation spectroscopy, we identified the strain ΔPtMAT1 as a producer of the diastereomer type of MEL-D instead of MEL-B.

摘要

甘露糖赤藓糖醇脂(MELs)是担子菌酵母利用原料生产的生物表面活性剂。MELs根据其结构表现出不同的性质,如乙酰化或酰化程度以及甘露糖赤藓糖醇部分的手性。筑波假丝酵母产生一种非对映异构体类型的MEL - B(单乙酰化MEL);因此,缺失乙酰转移酶可能会产生一种非对映异构体类型的MEL - D(去乙酰化MEL),而这种物质仅在以MEL - B为底物的脂肪酶体外反应中产生过。在此,我们通过靶向基因缺失技术,删除了筑波假丝酵母1E5中编码与MEL生物合成相关的乙酰转移酶的基因PtMAT1,并获得了非对映异构体类型MEL - D的产生菌。筑波假丝酵母1E5的尿嘧啶营养缺陷型突变体(PtURA5 - 突变体)被用作基因缺失的宿主菌株。以尿嘧啶营养缺陷作为选择标记,通过同源重组用PtURA5盒替换了基因PtMAT1。根据薄层色谱和核磁共振光谱分析,我们鉴定出ΔPtMAT1菌株是一种非对映异构体类型MEL - D而非MEL - B的产生菌。

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