Magnus Nancy, Weise Teresa, Piechulla Birgit
Institute for Biological Sciences, University of Rostock, Rostock, Germany.
EuroImmun, Medizinische Labordiagnostik AG, Lübeck, Germany.
Front Microbiol. 2017 Dec 19;8:2522. doi: 10.3389/fmicb.2017.02522. eCollection 2017.
Microorganisms are capable of synthesizing a plethora of secondary metabolites including the long-overlooked volatile organic compounds. Little knowledge has been accumulated regarding the regulation of the biosynthesis of such mVOCs. The emission of the unique compound sodorifen of isolates was significantly reduced in minimal medium with glucose, while succinate elevated sodorifen release. The hypothesis of carbon catabolite repression (CCR) acting as a major control entity on the synthesis of mVOCs was proven by genetic evidence. Central components of the typical CCR of Gram-negative bacteria such as the adenylate cyclase (CYA), the cAMP binding receptor protein (CRP), and the catabolite responsive element (CRE) were removed by insertional mutagenesis. CYA, CRP, CRE1 mutants revealed a lower sodorifen release. Moreover, the emission potential of other isolates was also evaluated.
微生物能够合成大量的次级代谢产物,包括长期被忽视的挥发性有机化合物。关于此类挥发性有机化合物生物合成的调控,目前积累的知识很少。在含有葡萄糖的基本培养基中,分离株独特化合物索多芬的释放量显著降低,而琥珀酸盐则提高了索多芬的释放量。碳分解代谢物阻遏(CCR)作为挥发性有机化合物合成的主要控制机制这一假说得到了遗传学证据的证实。通过插入诱变去除了革兰氏阴性菌典型CCR的核心成分,如腺苷酸环化酶(CYA)、cAMP结合受体蛋白(CRP)和分解代谢物反应元件(CRE)。CYA、CRP、CRE1突变体显示出较低的索多芬释放量。此外,还评估了其他分离株的释放潜力。