Tsai W C, Westby C A
J Bacteriol. 1978 Nov;136(2):582-7. doi: 10.1128/jb.136.2.582-587.1978.
Intact cells of Myxococcus xanthus were examined for de novo purine synthesis and salvage utilization. The cellular uptake rates of radioactive glycine (de novo purine precursor), adenine, and guanine were measured, and thin-layer chromatography and radioautography were used to examine cell extracts for de novo synthesized purine nucleotides. Intact vegatative cells, glycerol-induced myxospores, and germinating cells of M. xanthus CW-1 were able to carry out de novo purine and salvage synthesis. Germinating cells and glycerol-induced myxospores were metabolically more active or as active as vegetative cells with respect to purine anabolism. We conclude that M. xanthus is capable of synthesizing purine nucleotides and salvaging purines throughout the glycerol version of its life cycle.
对黄色粘球菌的完整细胞进行了从头嘌呤合成和补救利用的研究。测定了放射性甘氨酸(从头嘌呤前体)、腺嘌呤和鸟嘌呤的细胞摄取率,并使用薄层色谱法和放射自显影术检查细胞提取物中的从头合成嘌呤核苷酸。黄色粘球菌CW-1的完整营养细胞、甘油诱导的粘孢子和萌发细胞能够进行从头嘌呤合成和补救合成。就嘌呤合成代谢而言,萌发细胞和甘油诱导的粘孢子代谢活性更高或与营养细胞相当。我们得出结论,黄色粘球菌在其生命周期的甘油阶段能够合成嘌呤核苷酸并补救嘌呤。