Taranto María P, Vera José L, Hugenholtz Jeroen, De Valdez Graciela F, Sesma Fernando
Centro de Referencia para Lactobacilos (CERELA-CONICET) Instituto de Microbiología, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán, Tucumán, Argentina.
J Bacteriol. 2003 Sep;185(18):5643-7. doi: 10.1128/JB.185.18.5643-5647.2003.
We found that Lactobacillus reuteri CRL1098, a lactic acid bacterium isolated from sourdough, is able to produce cobalamin. The sugar-glycerol cofermentation in vitamin B(12)-free medium showed that this strain was able to reduce glycerol through a well-known cobalamin-dependent reaction with the formation of 1,3-propanediol as a final product. The cell extract of L. reuteri corrected the coenzyme B12 requirement of Lactobacillus delbrueckii subsp. lactis ATCC 7830 and allowed the growth of Salmonella enterica serovar Typhimurium (metE cbiB) and Escherichia coli (metE) in minimal medium. Preliminary genetic studies of cobalamin biosynthesis genes from L. reuteri allowed the identification of cob genes which encode the CobA, CbiJ, and CbiK enzymes involved in the cobalamin pathway. The cobamide produced by L. reuteri, isolated in its cyanide form by using reverse-phase high-pressure liquid chromatography, showed a UV-visible spectrum identical to that of standard cyanocobalamin (vitamin B12).
我们发现,从酸面团中分离出的乳酸菌罗伊氏乳杆菌CRL1098能够产生钴胺素。在不含维生素B12的培养基中进行糖-甘油共发酵表明,该菌株能够通过一种众所周知的依赖钴胺素的反应还原甘油,最终生成1,3-丙二醇。罗伊氏乳杆菌的细胞提取物可校正德氏乳杆菌乳酸亚种ATCC 7830对辅酶B12的需求,并使鼠伤寒沙门氏菌(metE cbiB)和大肠杆菌(metE)在基本培养基中生长。对罗伊氏乳杆菌钴胺素生物合成基因的初步遗传学研究,使得能够鉴定出编码参与钴胺素途径的CobA、CbiJ和CbiK酶的cob基因。通过反相高压液相色谱法以氰化物形式分离出的罗伊氏乳杆菌产生的钴胺酰胺,其紫外可见光谱与标准氰钴胺(维生素B12)的光谱相同。