Vincent S F, Bell P J, Bissinger P, Nevalainen K M
Burns Philp Technology and Research Centre, North Ryde, Sydney, Australia.
Lett Appl Microbiol. 1999 Feb;28(2):148-52. doi: 10.1046/j.1365-2672.1999.00487.x.
Yeast strains currently used in the baking industry cannot fully utilize the trisaccharide raffinose found in beet molasses due to the absence of melibiase (alpha-galactosidase) activity. To overcome this deficiency, the MEL1 gene encoding melibiase enzyme was introduced into baker's yeast by both classical breeding and recombinant DNA technology. Both types of yeast strains were capable of vigorous fermentation in the presence of high levels of sucrose, making them suitable for the rapidly developing Asian markets where high levels of sugar are used in bread manufacture. Melibiase expression appeared to be dosage-dependent, with relatively low expression sufficient for complete melibiose utilization in a model fermentation system.
目前烘焙行业使用的酵母菌株由于缺乏蜜二糖酶(α-半乳糖苷酶)活性,无法充分利用甜菜糖蜜中的三糖棉子糖。为了克服这一缺陷,通过传统育种和重组DNA技术将编码蜜二糖酶的MEL1基因导入面包酵母中。这两种酵母菌株在高浓度蔗糖存在的情况下都能进行旺盛发酵,使其适用于在面包制作中使用高糖量的快速发展的亚洲市场。蜜二糖酶的表达似乎呈剂量依赖性,在模型发酵系统中相对较低的表达量就足以完全利用蜜二糖。