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Camptothecin-producing endophytic fungus Trichoderma atroviride LY357: isolation, identification, and fermentation conditions optimization for camptothecin production

机译:产生喜树碱的内生真菌阿奇木霉LY357:喜树碱生产的分离,鉴定和发酵条件优化

摘要

Camptothecin (CPT), the third largest anticancer drug, is produced mainly by Camptotheca acuminata and Nothapodytes foetida. CPT itself is the starting material for clinical CPT-type drugs, but the plant-derived CPT cannot support the heavy demand from the global market. Research efforts have been made to identify novel sources for CPT. In this study, three CPT-producing endophytic fungi, Aspergillus sp. LY341, Aspergillus sp. LY355, and Trichoderma atroviride LY357, were isolated and identified from C. acuminata. Most CPT produced by these fungi was found in the fermentation broth, and their corresponding CPT yields were 7.93, 42.92, and 197.82 mu g l(-1), respectively. The CPT-producing capability of LY341 and LY355 was completely lost after repeat subculturing. A substantial decrease of CPT production was also observed in the second generation of LY357. However, a stable and sustainable production of CPT was found from the second generation through the eighth generation of LY357. The fermentation medium, time, pH, temperature, and agitation rate were optimized for CPT production. Methyl jasmonate and XAD16 were proven to be an optimum elicitor and adsorbent resin, respectively, in view of that CPT yield was increased 3.4- and 11-fold through their use. A 50- to 75-fold increase of CPT yield was obtained when the optimized fermentation conditions, elicitor, and adsorbent resin were combined and applied to the culture of the seventh and eighth generations of LY357, and the highest CPT yield was 142.15 mu g l(-1). The CPT-producing T. atroviride LY357 paves a potential to uncover the mysteries of CPT biosynthesis.
机译:喜树碱(CPT)是第三大抗癌药物,主要由喜树和喜怒无常生产。 CPT本身是临床CPT类药物的起始材料,但是植物衍生的CPT无法满足全球市场的大量需求。为了确定CPT的新颖来源,已经进行了研究工作。在这项研究中,三种产生CPT的内生真菌Aspergillus sp.。 LY341,曲霉菌。 LY355和木霉阿特罗韦肽LY357是从C. acuminata分离并鉴定的。在发酵液中发现了由这些真菌产生的大部分CPT,其相应的CPT产量分别为7.93、42.92和197.82微克l(-1)。重复传代后,LY341和LY355的CPT生产能力完全丧失。在第二代LY357中也观察到CPT产生的显着降低。然而,从第二代到第八代LY357,发现了稳定且可持续的CPT生产。优化发酵培养基,时间,pH,温度和搅拌速率以生产CPT。茉莉酸甲酯和XAD16分别被证明是最佳的引发剂和吸附树脂,因为使用它们可使CPT产量提高3.4倍和11倍。当将优化的发酵条件,引发剂和吸附树脂组合并应用于第七代和第八代LY357的培养时,CPT产量提高了50到75倍,最高CPT产量为142.15μg( -1)。产生CPT的Atroviride LY3​​57可能揭示CPT生物合成的奥秘。

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