Witkin S S, Rosenberg E
J Bacteriol. 1970 Sep;103(3):641-9. doi: 10.1128/jb.103.3.641-649.1970.
The induction of mycrocyst formation by methionine starvation was demonstrated in Myxococcus xanthus by several methods. Growing in a defined medium (M(1)), M. xanthus had a doubling time of 6.5 hr. Four amino acids-leucine, isoleucine, valine, and glycine-were required for growth under these conditions. When the concentration of several amino acids in the medium was reduced (M(2)), the doubling time increased to 10 to 12 hr, and a requirement for methionine was observed. Methionine starvation led to a slow conversion of the population to microcysts. Under conditions of methionine prototrophy (M(1)), microcyst formation could still be triggered in exponentially growing cells by the addition of either 5 mm ethionine or 0.1 m isoleucine plus 0.1 m threonine, feedback inhibitors of methionine biosynthesis. Vegetative growth in the absence of methionine was obtained in medium M(2) if the leucine concentration was raised to its level in medium M(1). Thus, methionine biosynthesis is controlled by the exogenous concentration of the required amino acid, leucine. During an examination of the effects of methionine metabolites on microcyst formation, the involvement of polyamines in morphogenesis was uncovered. Putrescine (0.05 m) induced the formation of microcysts; spermidine (2 to 5 mm) inhibited induction by methionine starvation, ethionine, or high isoleucine-threonine. Spermidine was the only polyamine detected in M. xanthus (16.0 mug/10(9) cells). Its concentration decreased by more than 50% shortly after microcyst induction by high isoleucine-threonine. It is postulated that spermidine is an inhibitor of microcyst induction; when spermidine formation is blocked by methionine starvation, morphogenesis is induced.
通过多种方法在黄色粘球菌中证明了蛋氨酸饥饿诱导微囊形成。在限定培养基(M(1))中生长时,黄色粘球菌的倍增时间为6.5小时。在这些条件下生长需要四种氨基酸——亮氨酸、异亮氨酸、缬氨酸和甘氨酸。当培养基中几种氨基酸的浓度降低(M(2))时,倍增时间增加到10至12小时,并且观察到对蛋氨酸的需求。蛋氨酸饥饿导致群体缓慢转化为微囊。在蛋氨酸原养型(M(1))条件下,通过添加5 mM乙硫氨酸或0.1 M异亮氨酸加0.1 M苏氨酸(蛋氨酸生物合成的反馈抑制剂),仍可在指数生长的细胞中触发微囊形成。如果将亮氨酸浓度提高到培养基M(1)中的水平,则在培养基M(2)中可在缺乏蛋氨酸的情况下实现营养生长。因此,蛋氨酸生物合成受所需氨基酸亮氨酸的外源浓度控制。在研究蛋氨酸代谢产物对微囊形成的影响时,发现了多胺参与形态发生。腐胺(0.05 M)诱导微囊形成;亚精胺(2至5 mM)抑制蛋氨酸饥饿、乙硫氨酸或高异亮氨酸 - 苏氨酸诱导的微囊形成。亚精胺是在黄色粘球菌中检测到的唯一多胺(16.0 μg/10(9)个细胞)。在高异亮氨酸 - 苏氨酸诱导微囊形成后不久,其浓度下降超过50%。据推测,亚精胺是微囊形成的抑制剂;当亚精胺的形成被蛋氨酸饥饿阻断时,形态发生被诱导。