Nambu-Nishida Yumiko, Sakihama Yuri, Ishii Jun, Hasunuma Tomohisa, Kondo Akihiko
Technology Research Association of Highly Efficient Gene Design (TRAHED), 7-1-49 Minatojimaminamimachi, Chuo-ku, Kobe 650-0047, Japan; Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.
Graduate School of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.
J Biosci Bioeng. 2018 Jan;125(1):76-86. doi: 10.1016/j.jbiosc.2017.08.001. Epub 2017 Aug 30.
To efficiently utilize xylose, a major sugar component of hemicelluloses, in Saccharomyces cerevisiae requires the proper expression of varied exogenous and endogenous genes. To expand the repertoire of promoters in engineered xylose-utilizing yeast strains, we selected promoters in S. cerevisiae during cultivation and fermentation using xylose as a carbon source. To select candidate promoters that function in the presence of xylose, we performed comprehensive gene expression analyses using xylose-utilizing yeast strains both during xylose and glucose fermentation. Based on microarray data, we chose 29 genes that showed strong, moderate, and weak expression in xylose rather than glucose fermentation. The activities of these promoters in a xylose-utilizing yeast strain were measured by lacZ reporter gene assays over time during aerobic cultivation and microaerobic fermentation, both in xylose and glucose media. In xylose media, P, P, and P were favorable for high expression, and P, P, P, P, P, and P were acceptable for medium-high expression in aerobic cultivation, and moderate expression in microaerobic fermentation. P allowed moderate expression in aerobic culture and weak expression in microaerobic fermentation, although it showed medium-high expression in glucose media. P and P allowed moderate expression in aerobic cultivation, while showing weak but clear expression in microaerobic fermentation. P and P showed moderate promoter activity in aerobic cultivation, but showed almost no activity in microaerobic fermentation. The knowledge of promoter activities in xylose cultivation obtained in this study will permit the control of gene expression in engineered xylose-utilizing yeast strains that are used for hemicellulose fermentation.
要在酿酒酵母中有效利用木糖(半纤维素的主要糖成分),需要多种外源和内源基因的正确表达。为了扩大工程化木糖利用酵母菌株中启动子的种类,我们在以木糖为碳源的培养和发酵过程中筛选了酿酒酵母中的启动子。为了筛选在木糖存在下起作用的候选启动子,我们使用木糖利用酵母菌株在木糖和葡萄糖发酵过程中进行了全面的基因表达分析。基于微阵列数据,我们选择了29个在木糖发酵而非葡萄糖发酵中表现出强、中、弱表达的基因。通过lacZ报告基因测定法,在有氧培养和微需氧发酵过程中,在木糖和葡萄糖培养基中随时间测量了这些启动子在木糖利用酵母菌株中的活性。在木糖培养基中,P、P和P有利于高表达,P、P、P、P、P和P在有氧培养中适合中高表达,在微需氧发酵中适合中等表达。P在有氧培养中允许中等表达,在微需氧发酵中允许弱表达,尽管它在葡萄糖培养基中表现出中高表达。P和P在有氧培养中允许中等表达,而在微需氧发酵中表现出弱但明显的表达。P和P在有氧培养中显示出中等启动子活性,但在微需氧发酵中几乎没有活性。本研究中获得的木糖培养中启动子活性的知识将有助于控制用于半纤维素发酵的工程化木糖利用酵母菌株中的基因表达。