Takahashi-Íñiguez Tóshiko, Barrios-Hernández Joana, Rodríguez-Maldonado Marion, Flores María Elena
Departamento de Biología Molecular y Biotecnología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.
Arch Microbiol. 2018 Nov;200(9):1279-1286. doi: 10.1007/s00203-018-1541-z. Epub 2018 Jun 23.
The oxidation of malate to oxaloacetate is catalysed only by a nicotinamide adenine dinucleotide-dependent malate dehydrogenase encoded by SCO4827 in Streptomyces coelicolor. A mutant lacking the malate dehydrogenase gene was isolated and no enzymatic activity was detected. As expected, the ∆mdh mutant was unable to grow on malate as the sole carbon source. However, the mutant grew less in minimal medium with glucose and there was a delay of 36 h. The same behaviour was observed when the mutant was grown on minimal medium with casamino acids or glycerol. For unknown reasons, the mutant was not able to grow in YEME medium with glucose. The deficiency of malate dehydrogenase affected the expression of the isocitrate dehydrogenase and alpha-ketoglutarate dehydrogenase genes, decreasing the expression of both genes by approximately two- to threefold.
苹果酸氧化为草酰乙酸仅由天蓝色链霉菌中SCO4827编码的烟酰胺腺嘌呤二核苷酸依赖性苹果酸脱氢酶催化。分离出一个缺乏苹果酸脱氢酶基因的突变体,未检测到酶活性。正如预期的那样,∆mdh突变体无法以苹果酸作为唯一碳源生长。然而,该突变体在含有葡萄糖的基本培养基中生长较慢,且有36小时的延迟。当突变体在含有酪蛋白氨基酸或甘油的基本培养基中生长时,也观察到了相同的行为。出于未知原因,该突变体无法在含有葡萄糖的YEME培养基中生长。苹果酸脱氢酶的缺乏影响了异柠檬酸脱氢酶和α-酮戊二酸脱氢酶基因的表达,使这两个基因的表达降低了约两到三倍。