Research Center for Biotechnology, LIPI, Cibinong 16911, West Java, Indonesia.
Department of Environmental and Life Sciences, School of Food and Nutritional Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan; Organization of Advanced Science and Technology, Kobe University, 1-1 Rokkodaicho, Nada-ku, Kobe 657-8501, Japan.
Bioresour Technol. 2017 Dec;245(Pt B):1400-1406. doi: 10.1016/j.biortech.2017.05.190. Epub 2017 Jun 1.
This work aims to produce glutathione directly from mannan-based bioresources using engineered Saccharomyces cerevisiae. Mannan proved to be a valuable carbon source for glutathione production by this organism. Mannan-hydrolyzing S. cerevisiae was developed by heterologous expression of mannanase/mannosidase on its cell surface. This strain efficiently produced glutathione from mannose polysaccharide, β-1,4-mannan. Furthermore, it produced glutathione from locust bean gum (LBG), a highly dense and inexpensive mannan-based bioresource, as sole carbon source. Glutathione productivity from LBG was enhanced by engineering the glutathione metabolism of mannan-hydrolyzing S. cerevisiae. Expression of extracellular mannanase/mannosidase protein combined with intracellular metabolic engineering is potentially applicable to the efficient, environmentally friendly bioproduction of targeted products from mannan-based bioresources.
本工作旨在利用工程化的酿酒酵母(Saccharomyces cerevisiae)直接从甘露聚糖基生物资源中生产谷胱甘肽。甘露聚糖被证明是该生物生产谷胱甘肽的有价值的碳源。甘露聚糖水解酿酒酵母通过在其细胞表面异源表达甘露聚糖酶/甘露糖苷酶来开发。该菌株可有效地从甘露糖多糖、β-1,4-甘露聚糖生产谷胱甘肽。此外,它还可以将罗望子豆胶(LBG)作为唯一的碳源生产谷胱甘肽,LBG 是一种高密度且廉价的甘露聚糖基生物资源。通过对甘露聚糖水解酿酒酵母的谷胱甘肽代谢进行工程改造,提高了 LBG 生产谷胱甘肽的能力。胞外甘露聚糖酶/甘露糖苷酶蛋白的表达与细胞内代谢工程相结合,有望应用于高效、环保地从甘露聚糖基生物资源中生产目标产物。