White R L, Ramezani M, Gharbia S E, Seth R, Doherty-Kirby A L, Shah H N
Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, Canada.
Biotechnol Appl Biochem. 1995 Dec;22(3):385-96.
Catabolism of glutamate was investigated in Fusobacterium nucleatum, an anaerobic micro-organism that is strongly implicated in periodontal disease. The distribution of labels in acetate and butyrate derived from [13C]glutamates was determined by NMR spectroscopy and MS. The label from L-[5-13C]glutamate was not incorporated, whereas C-1 of acetate and butyrate were efficiently labelled by L-[1-13C]glutamate; these results indicated that the hydroxyglutarate pathway predominated. In butyrate, enrichment at C-3 was smaller than C-1; that this was not due to participation of the methylaspartate pathway was demonstrated by the incorporation of label from L-[4-13C]glutamate into only C-2 of acetate and C-4 (major)/C-2 (minor) of butyrate. The presence of label at a second site in butyrate was attributed to the synthesis of butyrate from acetate and verified by the incorporation of label from [1,2-13C2]- and [2H3]-acetate.
在具核梭杆菌(一种与牙周疾病密切相关的厌氧微生物)中研究了谷氨酸的分解代谢。通过核磁共振光谱和质谱法测定了源自[¹³C]谷氨酸的乙酸盐和丁酸盐中标记物的分布。L-[5-¹³C]谷氨酸的标记未被掺入,而乙酸盐和丁酸盐的C-1被L-[1-¹³C]谷氨酸有效地标记;这些结果表明羟基戊二酸途径占主导。在丁酸盐中,C-3处的富集小于C-1;L-[4-¹³C]谷氨酸的标记仅掺入乙酸盐的C-2和丁酸盐的C-4(主要)/C-2(次要),这证明这不是由于甲基天冬氨酸途径的参与。丁酸盐中第二个位点存在标记归因于由乙酸盐合成丁酸盐,并通过[1,2-¹³C₂]-和[²H₃]-乙酸盐的标记掺入得到证实。