Brickwedde Anja, Brouwers Nick, van den Broek Marcel, Gallego Murillo Joan S, Fraiture Julie L, Pronk Jack T, Daran Jean-Marc G
Department of Biotechnology, Delft University of Technology, Delft, Netherlands.
Front Microbiol. 2018 Aug 10;9:1786. doi: 10.3389/fmicb.2018.01786. eCollection 2018.
lager brewing yeasts are domesticated hybrids of and cold-tolerant . To understand the contribution of both parental genomes to maltose metabolism in brewing wort, this study focuses on maltose transport in the type strain CBS 12357/FM1318. To obtain complete sequences of the loci of this strain, a near-complete genome assembly was generated using the Oxford Nanopore Technology MinION sequencing platform. Except for CHRXII, all sixteen chromosomes were assembled as single contigs. Four loci harboring putative maltose transporter genes (), located in subtelomeric regions of CHRII, CHRV, CHRXIII, and CHRXVI, were completely resolved. The near-identical loci on CHRV and CHRXVI strongly resembled canonical loci, while those on CHRII and CHRXIII showed different structures suggestive of gene loss. Overexpression of in a maltose-transport-deficient strain restored growth on maltose, but not on maltotriose, indicating maltose-specific transport functionality of all four transporters. Simultaneous CRISPR-Cas9-assisted deletion of only and , which shared 99.7% sequence identity, eliminated growth of CBS 12357 on maltose. Transcriptome analysis of CBS 12357 established that and , are poorly expressed in maltose-grown cultures, while and were expressed at much higher levels than and , indicating that only are responsible for maltose consumption in CBS 12357. These results represent a first genomic and physiological characterization of maltose transport in CBS 12357 and provides a valuable resource for further industrial exploitation of this yeast.
拉格啤酒酿造酵母是驯化的杂交种,兼具[未提及的某种特性]和耐寒性。为了解双亲基因组对麦芽汁中麦芽糖代谢的贡献,本研究聚焦于[未提及的某种酵母]型菌株CBS 12357/FM1318中的麦芽糖转运。为获得该菌株麦芽糖转运蛋白基因座的完整序列,使用牛津纳米孔技术MinION测序平台生成了近乎完整的基因组组装。除了CHRXII,所有16条染色体都组装为单个重叠群。位于CHRII、CHRV、CHRXIII和CHRXVI亚端粒区域的四个含有假定麦芽糖转运蛋白基因([未提及具体基因名称])的基因座被完全解析。CHRV和CHRXVI上几乎相同的基因座与典型的[未提及的某种基因座]非常相似,而CHRII和CHRXIII上的基因座显示出不同的结构,提示基因丢失。在缺乏麦芽糖转运功能的[未提及的某种菌株]中过表达[未提及的基因]可恢复在麦芽糖上的生长,但在麦芽三糖上不能恢复,表明所有四种转运蛋白都具有麦芽糖特异性转运功能。仅同时利用CRISPR-Cas9辅助敲除序列同一性为99.7%的[未提及的两个基因],消除了[未提及的某种酵母]CBS 12357在麦芽糖上的生长。对[未提及的某种酵母]CBS 12357的转录组分析表明,[未提及的两个基因]在以麦芽糖为生长底物的培养物中表达水平较低,而[未提及的另外两个基因]的表达水平远高于[未提及的两个基因],表明在CBS 12357中只有[未提及的两个基因]负责麦芽糖的消耗。这些结果代表了对[未提及的某种酵母]CBS 12357中麦芽糖转运的首次基因组和生理学特征描述,并为该酵母的进一步工业开发提供了宝贵资源。