Bellion E, Kirkley D H
Biochim Biophys Acta. 1977 Mar 29;497(1):323-8. doi: 10.1016/0304-4165(77)90166-0.
The mode of biosynthesis of the thiazole moiety of thiamine, 4-methyl-5beta-hydroxyethyl thiazole (MHET) was studied using Salmonella typhimurium as test organism. It was shown by isotope incorporation experiments, that the sulfur atom, but not carbon-3, of cysteine is incorporated into MHET, indicating a separation of the sulfur atom of cysteine from the carbon chain during incorporation. Isotope competition experiments revealed that the incorporation of [35S]cysteine is not significantly diluted by the presence of methionine, homocysteine, and glutathione. No incorporation of label from [14C]glutamate and [14C]formate was observed, leaving the origin of the five-carbon unit still in doubt.
利用鼠伤寒沙门氏菌作为测试生物,对硫胺素的噻唑部分,即4-甲基-5β-羟乙基噻唑(MHET)的生物合成模式进行了研究。同位素掺入实验表明,半胱氨酸的硫原子而非碳-3被掺入到MHET中,这表明在掺入过程中半胱氨酸的硫原子与碳链分离。同位素竞争实验显示,甲硫氨酸、高半胱氨酸和谷胱甘肽的存在并不会显著稀释[35S]半胱氨酸的掺入。未观察到[14C]谷氨酸和[14C]甲酸的标记掺入,五碳单元的来源仍不确定。