Germinario R J, Waller J R
Can J Microbiol. 1976 Mar;22(3):347-53. doi: 10.1139/m76-053.
Non-proliferating cells of Lactobacillus plantarum accumulated about 1.3 mug of pantothenic acid (PA) per milligram dry cells when placed in a phosphate-buffered solution containing glucose, NaCl, and PA for 21 h. Under the conditions applied for PA uptake, pH 7.5 and 38 degrees C, the accumulated PA existed almost exclusively in a bound form. Free PA was observed only occasionally and then at questionably significant levels. All bound PA was released quantitatively by enzyme hydrolysis with alkaline (intestinal) phosphatase. Chromatographic analysis coupled with differential microbiological analysis of cell extracts using Saccharomyces cerevisiae, Lactobacillus helveticus, and L. plantarum identified the accumulated PA as phosphopantothenic acid (P-PA). Assay of P-PA loaded cell extracts (devoid of free PA) by L. plantarum before and after alkaline phosphatase hydrolysis showed that the growth of this primary assay organism was stimulated by 8.3%.
将植物乳杆菌的非增殖细胞置于含有葡萄糖、氯化钠和泛酸的磷酸盐缓冲溶液中21小时后,每毫克干细胞积累了约1.3微克泛酸(PA)。在用于摄取PA的条件下,pH值为7.5,温度为38℃,积累的PA几乎完全以结合形式存在。仅偶尔观察到游离PA,且其含量是否具有显著意义存疑。所有结合的PA通过用碱性(肠道)磷酸酶进行酶水解而定量释放。使用酿酒酵母、瑞士乳杆菌和植物乳杆菌对细胞提取物进行色谱分析并结合差异微生物分析,确定积累的PA为磷酸泛酸(P-PA)。在碱性磷酸酶水解前后,用植物乳杆菌对加载了P-PA的细胞提取物(不含游离PA)进行测定,结果表明这种主要检测生物体的生长受到了8.3%的刺激。