Institute for Wine Biotechnology, Stellenbosch University, Stellenbosch, Western Cape, South Africa.
PLoS One. 2013 Oct 11;8(10):e77499. doi: 10.1371/journal.pone.0077499. eCollection 2013.
Levans are fructose polymers synthesized by a broad range of micro-organisms and a limited number of plant species as non-structural storage carbohydrates. In microbes, these polymers contribute to the formation of the extracellular polysaccharide (EPS) matrix and play a role in microbial biofilm formation. Levans belong to a larger group of commercially important polymers, referred to as fructans, which are used as a source of prebiotic fibre. For levan, specifically, this market remains untapped, since no viable production strategy has been established. Synthesis of levan is catalysed by a group of enzymes, referred to as levansucrases, using sucrose as substrate. Heterologous expression of levansucrases has been notoriously difficult to achieve in Saccharomyces cerevisiae. As a strategy, this study used an invertase (Δsuc2) null mutant and two separate, engineered, sucrose accumulating yeast strains as hosts for the expression of the levansucrase M1FT, previously cloned from Leuconostoc mesenteroides. Intracellular sucrose accumulation was achieved either by expression of a sucrose synthase (Susy) from potato or the spinach sucrose transporter (SUT). The data indicate that in both Δsuc2 and the sucrose accumulating strains, the M1FT was able to catalyse fructose polymerisation. In the absence of the predicted M1FT secretion signal, intracellular levan accumulation was significantly enhanced for both sucrose accumulation strains, when grown on minimal media. Interestingly, co-expression of M1FT and SUT resulted in hyper-production and extracellular build-up of levan when grown in rich medium containing sucrose. This study presents the first report of levan production in S. cerevisiae and opens potential avenues for the production of levan using this well established industrial microbe. Furthermore, the work provides interesting perspectives when considering the heterologous expression of sugar polymerizing enzymes in yeast.
低聚糖是由广泛的微生物和有限数量的植物物种作为非结构性储存碳水化合物合成的果糖聚合物。在微生物中,这些聚合物有助于形成细胞外多糖 (EPS) 基质,并在微生物生物膜形成中发挥作用。低聚糖属于一组更具商业重要性的聚合物,称为果聚糖,它们被用作益生元纤维的来源。就低聚糖而言,由于尚未建立可行的生产策略,因此这个市场尚未开发。低聚糖的合成由一组称为 levansucrases 的酶催化,使用蔗糖作为底物。在酿酒酵母中,异源表达 levansucrases 一直非常困难。作为一种策略,本研究使用了一种蔗糖酶 (Δsuc2) 缺失突变体和两种单独的、工程化的蔗糖积累酵母菌株作为先前从肠膜明串珠菌克隆的 levansucrase M1FT 的表达宿主。通过表达来自马铃薯的蔗糖合酶 (Susy) 或菠菜蔗糖转运蛋白 (SUT) 实现细胞内蔗糖积累。数据表明,在 Δsuc2 和蔗糖积累菌株中,M1FT 都能够催化果糖聚合。在缺乏预测的 M1FT 分泌信号的情况下,当在最小培养基上生长时,两种蔗糖积累菌株的细胞内低聚糖积累显著增强。有趣的是,当在含有蔗糖的丰富培养基中生长时,共表达 M1FT 和 SUT 导致低聚糖的超生产和细胞外积累。本研究首次报道了酿酒酵母中低聚糖的生产,并为使用这种成熟的工业微生物生产低聚糖开辟了潜在途径。此外,当考虑在酵母中异源表达糖聚合酶时,这项工作提供了有趣的视角。