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Optimization of a chemically defined medium for mycelial growth and polysaccharide production by medicinal mushroom Phellinus igniarius

机译:化学定义的药用菌桑黄菌丝体生长和多糖生产培养基的优化

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摘要

A chemically defined medium for mycelial growth and exopolysaccharide (EPS) production by submerged culture of Phellinus igniarius was investigated. The mainly defined medium compositions were optimized by using orthogonal matrix method. The optimal defined medium (per liter) was 40.0 g glucose, 4.0 g. glutamic acid, 4.0 g (NH)SO, and initial pH 6.0. Under the optimal medium, the maximal mycelial biomass and EPS production were 12.33 pl 0.89 and 1.21 pl 0.08 g lp# at 192 h in shake flask, while the maximal mycelial biomass and EPS production reached 13.86 pl 0.52 and 1.92 pl 0.07 g lp# at 168 h in 3 l fermenter, respectively. The molecular weights (g molp#) of four fractions isolated from EPS by gel permeation were about 6.4 c 10e, 3.3 c 10e, 2.7 c 10e and 2.9 c 10pd. This study should be widely applied to other secondary metabolites production from higher fungus in a chemically defined medium and quantitative regulation of the metabolic flux in polysaccharide biosynthesis.
机译:研究了一种化学定义的培养基,用于通过桑黄的深层培养进行菌丝体生长和胞外多糖(EPS)的生产。使用正交矩阵法优化了主要定义的培养基组成。最佳定义培养基(每升)为40.0克葡萄糖,4.0克。谷氨酸,4.0 g(NH)SO和初始pH 6.0。在最佳培养基下,摇瓶在192 h的最大菌丝生物量和EPS产量分别为12.33 pl 0.89和1.21 pl 0.08 g lp#,而在发酵培养基中,最大的菌丝生物量和EPS产量分别为13.86 pl 0.52和1.92 pl 0.07 g lp#。在3升发酵罐中分别放置168小时。通过凝胶渗透从EPS分离出的四个馏分的分子量(g molp#)为约6.4c 10e,3.3c 10e,2.7c 10e和2.9c 10pd。该研究应广泛应用于在化学成分确定的培养基中由高级真菌生产的其他次级代谢产物,以及多糖生物合成中代谢通量的定量调节。

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