Manteca Angel, Alvarez Ruben, Salazar Nuria, Yagüe Paula, Sanchez Jesus
Area de Microbiologia, Departamento de Biologia Funcional and IUBA, Facultad de Medicina, Universidad de Oviedo, 33006 Oviedo, Spain.
Appl Environ Microbiol. 2008 Jun;74(12):3877-86. doi: 10.1128/AEM.02715-07. Epub 2008 Apr 25.
Despite the fact that most industrial processes for secondary metabolite production are performed with submerged cultures, a reliable developmental model for Streptomyces under these culture conditions is lacking. With the exception of a few species which sporulate under these conditions, it is assumed that no morphological differentiation processes take place. In this work, we describe new developmental features of Streptomyces coelicolor A3(2) grown in liquid cultures and integrate them into a developmental model analogous to the one previously described for surface cultures. Spores germinate as a compartmentalized mycelium (first mycelium). These young compartmentalized hyphae start to form pellets which grow in a radial pattern. Death processes take place in the center of the pellets, followed by growth arrest. A new multinucleated mycelium with sporadic septa (second mycelium) develops inside the pellets and along the periphery, giving rise to a second growth phase. Undecylprodigiosin and actinorhodin antibiotics are produced by this second mycelium but not by the first one. Cell density dictates how the culture will behave in terms of differentiation processes and antibiotic production. When diluted inocula are used, the growth arrest phase, emergence of a second mycelium, and antibiotic production are delayed. Moreover, pellets are less abundant and have larger diameters than in dense cultures. This work is the first to report on the relationship between differentiation processes and secondary metabolite production in submerged Streptomyces cultures.
尽管大多数用于生产次级代谢产物的工业过程都是在深层培养条件下进行的,但目前仍缺乏一种适用于这些培养条件下链霉菌的可靠发育模型。除了少数在这些条件下能形成孢子的物种外,一般认为在这些条件下不会发生形态分化过程。在这项研究中,我们描述了天蓝色链霉菌A3(2)在液体培养中的新发育特征,并将其整合到一个类似于先前描述的表面培养的发育模型中。孢子萌发形成分隔菌丝体(第一菌丝体)。这些年轻的分隔菌丝开始形成呈放射状生长的菌球。菌球中心会发生死亡过程,随后生长停止。一种新的具有零星隔膜的多核菌丝体(第二菌丝体)在菌球内部和周边发育,从而引发第二个生长阶段。十一烷基灵菌红素和放线紫红素抗生素由第二菌丝体产生,而第一菌丝体不产生。细胞密度决定了培养物在分化过程和抗生素生产方面的表现。当使用稀释接种物时,生长停滞期、第二菌丝体的出现以及抗生素生产都会延迟。此外,与高密度培养相比,菌球数量更少且直径更大。这项工作首次报道了深层链霉菌培养中分化过程与次级代谢产物生产之间的关系。