Tang C T, Engel R, Tropp B E
Antimicrob Agents Chemother. 1977 Jan;11(1):147-53. doi: 10.1128/AAC.11.1.147.
At a concentration of 2.5 mM, dl-glyceraldehyde 3-phosphate has a bactericidal effect upon Escherichia coli. The glycerol 3-phosphate transport system is required for the entry of the biologically active l-enantiomer. l-Glyceraldehyde must be phosphorylated by the cell to exert its full effect upon growth. The addition of dl-glyceraldehyde 3-phosphate to a culture of E. coli caused no preferential inhibition of the accumulation of deoxyribonucleic acid, ribonucleic acid, or phosphoglycerides, although protein accumulation was less affected. Studies with mutant strains ruled out catabolic glycerol 3-phosphate dehydrogenase, anabolic nicotinamide adenine dinucleotide (phosphate):sn-glycerol 3-phosphate oxidoreductase, and fructose 1,6-diphosphate aldolase as the primary sites of action. l-Glyceraldehyde 3-phosphate is a competitive inhibitor of sn-glycerol 3-phosphate in the reactions catalyzed by acyl coenzyme A:sn-glycerol 3-phosphate acyltransferase (K(i) of 1.8 mM) and cytidine 5'-diphosphate-diglyceride:sn-glycerol 3-phosphate phosphatidyltransferase (K(i) of 2.7 mM). A K(m) mutant for the former enzyme was susceptible to the inhibitor. l-Glyceraldehyde 3-phosphate does not affect acyl coenzyme A:lysophosphatidate acyltransferase activity. In vivo, phosphatidylethanolamine and phosphatidylglycerol accumulation are inhibited to the same extent by the addition of dl-glyceraldehyde 3-phosphate to a culture of E. coli.
在浓度为2.5 mM时,dl-3-磷酸甘油醛对大肠杆菌具有杀菌作用。生物活性l-对映体的进入需要3-磷酸甘油转运系统。l-甘油醛必须被细胞磷酸化才能对生长发挥其全部作用。向大肠杆菌培养物中添加dl-3-磷酸甘油醛不会优先抑制脱氧核糖核酸、核糖核酸或磷酸甘油酯的积累,尽管蛋白质积累受影响较小。对突变菌株的研究排除了分解代谢的3-磷酸甘油脱氢酶、合成代谢的烟酰胺腺嘌呤二核苷酸(磷酸):sn-3-磷酸甘油氧化还原酶和1,6-二磷酸果糖醛缩酶作为主要作用位点。在由酰基辅酶A:sn-3-磷酸甘油酰基转移酶(K(i)为1.8 mM)和胞苷5'-二磷酸二甘油酯:sn-3-磷酸甘油磷脂酰转移酶(K(i)为2.7 mM)催化的反应中,l-3-磷酸甘油醛是sn-3-磷酸甘油的竞争性抑制剂。前一种酶的K(m)突变体对该抑制剂敏感。l-3-磷酸甘油醛不影响酰基辅酶A:溶血磷脂酸酰基转移酶活性。在体内,向大肠杆菌培养物中添加dl-3-磷酸甘油醛会同等程度地抑制磷脂酰乙醇胺和磷脂酰甘油的积累。