Laycock M, McInnes A G, Walter J A, Shapiro S, Vining L C
Can J Microbiol. 1985 Jul;31(7):629-34. doi: 10.1139/m85-119.
To obtain information on the route(s) of ammonium assimilation in Streptomyces venezuelae, cell suspensions transferred to fresh medium lacking nitrogen were pulsed with [15N2]ammonium sulphate. Cells and extracellular fluids were examined by nuclear magnetic resonance and amino acid analysis to assess changes in amino acid pools and the disposition of [15N]ammonium. Following addition of [15N]ammonium, glutamate--glutamine pools of low cell density replacement cultures expanded rapidly and became progressively labelled with 15N, whereas the alanine pool size increased much more slowly and became labelled with 15N to a much lesser extent. These results are consistent with the assimilation of ammonium via glutamate dehydrogenase or glutamine synthetase--glutamate synthase rather than alanine dehydrogenase. Under anaerobic conditions, S. venezuelae assimilates ammonium into alanine rather than glutamate--glutamine. Alanine dehydrogenase may thus function as a vehicle to regenerate NAD+ to maintain substrate-level phosphorylation during periods of anaerobiosis.
为了获取委内瑞拉链霉菌中铵同化途径的信息,将转移至缺乏氮的新鲜培养基中的细胞悬液用[15N2]硫酸铵进行脉冲处理。通过核磁共振和氨基酸分析检查细胞和细胞外液,以评估氨基酸库的变化和[15N]铵的去向。添加[15N]铵后,低密度替代培养物的谷氨酸-谷氨酰胺库迅速扩大,并逐渐被15N标记,而丙氨酸库的大小增加得慢得多,且被15N标记的程度也小得多。这些结果与通过谷氨酸脱氢酶或谷氨酰胺合成酶-谷氨酸合酶而不是丙氨酸脱氢酶进行铵同化一致。在厌氧条件下,委内瑞拉链霉菌将铵同化为丙氨酸而不是谷氨酸-谷氨酰胺。因此,丙氨酸脱氢酶可能作为一种载体来再生NAD+,以在厌氧期间维持底物水平磷酸化。