Birnbaum J, Pai C H, Lichstein H C
J Bacteriol. 1967 Dec;94(6):1846-53. doi: 10.1128/jb.94.6.1846-1853.1967.
Use of a yeast-lactobacillus differential microbiological assay permitted investigation into the synthesis of biotin vitamers by a variety of bacteria. A major portion of the biotin activity was found extracellularly. The level of total biotin (assayable with yeast) greatly exceeded the level of true biotin (assayed with lactobacillus). Values for intracellular biotin generally showed good agreement between the assays, suggesting the presence of only true biotin within the cells. Bioautographic analysis of the medium after growth of each organism revealed the presence of large amounts of a vitamer which corresponded to dl-desthiobiotin on the basis of Rf value and biological activity. Biotin, when detected at all, was at very low concentrations. Also, an avidin-uncombinable vitamer was synthesized by a majority of the bacteria. Addition of d-biotin to the growth medium prevented completely the synthesis of both vitamers of biotin. d-Biotin-d-sulfoxide had no effect on the synthesis of desthiobiotin or the avidin-uncombinable vitamer. Addition of dl-desthiobiotin did not prevent its own synthesis nor that of the other vitamer. Control of vitamer synthesis is therefore highly specific for d-biotin. The avidin-uncombinable vitamer was produced only at repressed levels in the presence of high concentrations of both d-biotin and dl-desthiobiotin, which suggested that it is not a degradation product of these substances. A possible mechanism for the overproduction of the biosynthetic precursors of biotin is presented.
使用酵母 - 乳酸杆菌差异微生物测定法能够研究多种细菌对生物素维生素异构体的合成情况。发现大部分生物素活性存在于细胞外。总生物素(用酵母测定)的水平大大超过真正生物素(用乳酸杆菌测定)的水平。细胞内生物素的值在两种测定方法之间通常显示出良好的一致性,这表明细胞内仅存在真正的生物素。对每种生物体生长后的培养基进行生物自显影分析,发现存在大量维生素异构体,根据比移值和生物活性,其与dl - 脱硫生物素相对应。生物素即便被检测到,浓度也非常低。此外,大多数细菌合成了一种抗生物素蛋白不可结合的维生素异构体。向生长培养基中添加d - 生物素可完全阻止生物素两种维生素异构体的合成。d - 生物素 - d - 亚砜对脱硫生物素或抗生物素蛋白不可结合的维生素异构体的合成没有影响。添加dl - 脱硫生物素并不能阻止其自身的合成,也不能阻止另一种维生素异构体的合成。因此,维生素异构体合成的控制对d - 生物素具有高度特异性。在高浓度的d - 生物素和dl - 脱硫生物素存在下,抗生物素蛋白不可结合的维生素异构体仅在受抑制的水平产生,这表明它不是这些物质的降解产物。本文提出了生物素生物合成前体过量产生的一种可能机制。