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Two Ser/Thr protein kinases essential for efficient aggregation and spore morphogenesis in Myxococcus xanthus

机译:两个Ser / Thr蛋白激酶对于黄色粘球菌的有效聚集和孢子形态发生必不可少

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Myxococcus xanthus has a complex life cycle that involves vegetative growth and development. Previously, we described the espAB locus that is involved in timing events during the initial stages of fruiting body formation. Deletion of espA caused early aggregation and sporulation, whereas deletion of espB caused delayed aggregation and sporulation resulting in reduced spore yields. In this study, we describe two genes, pktA5 and pktB8, that flank the espAB locus and encode Ser/Thr protein kinase (STPK) homologues. Cells deficient in pktA5 or pktB8 formed translucent mounds and produced low spore yields, similar in many respects to espB mutants. Double mutant analysis revealed that espA was epistatic to pktA5 and pktB8 with respect to aggregation and fruiting body morphology, but that pktA5 and pktB8 were epistatic to espA with respect to sporulation efficiency. Expression profiles of pktA5-lacZ and pktB8-lacZ fusions and Western blot analysis showed that the STPKs are expressed under vegetative and developmental conditions. In vitro kinase assays demonstrated that the RD kinase, PktA5, autophosphorylated on threonine residue(s) and phosphorylated the artificial substrate, myelin basic protein. In contrast, autophosphorylation of the non-RD kinase, PktB8, was not observed in vitro; however, the phenotype of a pktB8 kinase-dead point mutant resembled the pktB8 deletion mutant, indicating that this residue was important for function and that it likely functions as a kinase in vivo. Immunoprecipitation Tap-tagged PktA5 and PktB8 revealed an interaction with EspA during development in M. xanthus. These results, taken together, suggest that PktA5 and PktB8 are STPKs that function during development by interacting with EspA and EspB to regulate M. xanthus development.
机译:黄腐粘球菌具有复杂的生命周期,涉及营养生长和发育。先前,我们描述了子实体形成初始阶段中与计时事件有关的espAB基因座。 espA的缺失引起早期的聚集和孢子形成,而espB的缺失引起延迟的聚集和孢子形成导致孢子产量降低。在这项研究中,我们描述了espAB基因座侧翼并编码Ser / Thr蛋白激酶(STPK)同源物的两个基因pktA5和pktB8。缺乏pktA5或pktB8的细胞形成半透明的丘丘,产生的孢子产量低,在许多方面与espB突变体相似。双重突变体分析显示,就聚集和子实体形态而言,espA对pktA5和pktB8具有上位性,但就孢子形成效率而言,pktA5和pktB8对espA具有上位性。 pktA5-lacZ和pktB8-lacZ融合蛋白的表达谱和Western blot分析表明,STPKs在营养和发育条件下表达。体外激酶测定表明,RD激酶PktA5在苏氨酸残基上自磷酸化,并在人工底物髓磷脂碱性蛋白上磷酸化。相反,在体外未观察到非RD激酶PktB8的自磷酸化。然而,pktB8激酶死亡点突变体的表型类似于pktB8缺失突变体,表明该残基对功能很重要,并且可能在体内起激酶的作用。免疫沉淀Tap-tagged PktA5和PktB8揭示了在X.xanthus发育过程中与EspA的相互作用。这些结果加在一起表明,PktA5和PktB8是STPK,它们在开发过程中通过与EspA和EspB相互作用来调节黄花木霉的发育。

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