Molecular Cell Biology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Kluyver Centre for Genomics of Industrial Fermentation, P.O. Box 14, 9750 AA Haren, The Netherlands.
Appl Environ Microbiol. 2010 Sep;76(17):5702-9. doi: 10.1128/AEM.02327-09. Epub 2010 Jul 2.
In the fungus Penicillium chrysogenum, penicillin (PEN) production is compartmentalized in the cytosol and in peroxisomes. Here we show that intact peroxisomes that contain the two final enzymes of PEN biosynthesis, acyl coenzyme A (CoA):6-amino penicillanic acid acyltransferase (AT) as well as the side-chain precursor activation enzyme phenylacetyl CoA ligase (PCL), are crucial for efficient PEN synthesis. Moreover, increasing PEN titers are associated with increasing peroxisome numbers. However, not all conditions that result in enhanced peroxisome numbers simultaneously stimulate PEN production. We find that conditions that lead to peroxisome proliferation but simultaneously interfere with the normal physiology of the cell may be detrimental to antibiotic production. We furthermore show that peroxisomes develop in germinating conidiospores from reticule-like structures. During subsequent hyphal growth, peroxisome proliferation occurs at the tip of the growing hyphae, after which the organelles are distributed over newly formed subapical cells. We observed that the organelle proliferation machinery requires the dynamin-like protein Dnm1.
在真菌青霉中,青霉素(PEN)的生产被分隔在细胞质和过氧化物酶体中。在这里,我们表明,含有 PEN 生物合成的最后两种酶,酰基辅酶 A(CoA):6-氨基青霉素酸酰基转移酶(AT)以及侧链前体激活酶苯乙酰辅酶 A 连接酶(PCL)的完整过氧化物酶体对于有效 PEN 合成至关重要。此外,增加过氧化物酶体的数量与增加 PEN 产量相关。然而,并非所有导致过氧化物酶体数量增加的条件同时刺激 PEN 产生。我们发现,导致过氧化物酶体增殖但同时干扰细胞正常生理的条件可能对抗生素生产有害。我们还表明,过氧化物体从网状结构在发芽的分生孢子中发育。在随后的菌丝生长过程中,过氧化物酶体增殖发生在生长菌丝的尖端,之后细胞器分布在新形成的亚顶端细胞上。我们观察到细胞器增殖机制需要类似于动力蛋白的蛋白 Dnm1。