Department of Food Science and Nutrition, University of Minnesota, St. Paul, Minnesota 55108.
Appl Environ Microbiol. 1979 Feb;37(2):316-23. doi: 10.1128/aem.37.2.316-323.1979.
The use of Streptococcus diacetylactis as a flavor producer in dairy fermentations is dependent upon its ability to produce diacetyl from citrate. Treatment of S. diacetylactis strains 18-16 and DRC1 with acridine orange resulted in the conversion of approximately 2% of the DRC1 population and 20% of the 18-16 population to citrate negative, which is indicative of the involvement of plasmid deoxyribonucleic acid (DNA). Growth in the presence of acridine orange also resulted in the appearance of 2% lactose-negative derivatives in S. diacetylactis 18-16 and 99% lactose-defective, proteinase-negative derivatives in S. diacetylactis DRC1. Cesium chloride-ethidium bromide equilibrium density gradients of cleared lysate material from each strain revealed the presence of covalently closed circular DNA. Samples of this covalently closed circular DNA were subjected to agarose gel electrophoresis to determine the plasmid composition of each strain. S. diacetylactis 18-16 was found to possess six plasmids, of approximately 41, 28, 6.4, 5.5, 3.4, and 3.0 megadaltons (Mdal). S. diacetylactis DRC1 contained six plasmids, of approximately 41, 31, 18, 5.5, 4.5, and 3.7 Mdal. Variants of S. diacetylactis 18-16 which failed to produce acetoin plus diacetyl from citrate (citrate negative) were missing a 5.5-Mdal plasmid. Lactose-negative mutants of the same strain were devoid of a 41-Mdal plasmid. Lactose-defective, proteinase-negative mutants of S. diacetylactis DRC1 were missing a 31-Mdal plasmid. The citrate-negative mutants of S. diacetylactis DRC1 isolated in this study did not possess a 5.5-Mdal plasmid. Thus, we have evidence that there is a correlation between the ability to utilize citrate and the presence of a 5.5-Mdal plasmid. A relationship was also noted between lactose fermentation and proteinase activity and plasmid DNA in S. diacetylactis.
唾液链球菌嗜热亚种作为一种风味产生菌在乳制品发酵中的应用依赖于其将柠檬酸盐转化为双乙酰的能力。吖啶橙处理唾液链球菌 18-16 株和 DRC1 株后,约有 2%的 DRC1 群体和 20%的 18-16 群体转化为柠檬酸盐阴性,这表明涉及质粒脱氧核糖核酸(DNA)。吖啶橙存在时的生长也导致唾液链球菌 18-16 中出现 2%乳糖阴性衍生物,而唾液链球菌 DRC1 中出现 99%乳糖缺陷、蛋白酶阴性衍生物。用氯化铯-溴化乙锭平衡密度梯度法对各菌株的澄清裂解物进行分析,发现存在共价闭合环状 DNA。对这种共价闭合环状 DNA 的样本进行琼脂糖凝胶电泳,以确定各菌株的质粒组成。发现唾液链球菌 18-16 含有六个质粒,大小约为 41、28、6.4、5.5、3.4 和 3.0 兆道尔顿(Mdal)。唾液链球菌 DRC1 含有六个质粒,大小约为 41、31、18、5.5、4.5 和 3.7 Mdal。不能从柠檬酸盐生产乙酰基丙酮加双乙酰(柠檬酸盐阴性)的唾液链球菌 18-16 变体缺失一个 5.5-Mdal 质粒。同一菌株的乳糖阴性突变体缺乏一个 41-Mdal 质粒。唾液链球菌 DRC1 的乳糖缺陷、蛋白酶阴性突变体缺失一个 31-Mdal 质粒。在本研究中分离的唾液链球菌 DRC1 的柠檬酸盐阴性突变体不具有 5.5-Mdal 质粒。因此,我们有证据表明利用柠檬酸盐的能力与 5.5-Mdal 质粒的存在之间存在相关性。在唾液链球菌中还观察到乳糖发酵与蛋白酶活性和质粒 DNA 之间存在关系。