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Strategies to enhance the production of pinoresinol and its glucosides by endophytic fungus (Phomopsis sp. XP-8) isolated from Tu-chung bark

机译:从土中树皮中分离的内生真菌(Phomopsis sp。XP-8)提高松油醇和葡萄糖苷生产的策略

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摘要

To improve the production yield of (+)-pinoresinol (Pin), (+)-pinoresinol monoglucoside (PMG), and (+)-pinoresinol diglucoside (PDG), different methods were conducted, including co-culture with resveratrol-producing Alternaria sp. MG1 spores and addition of Tu-chung in a medium at the start of cultivation, ultrasound treatment (40 kHZ, 10 min) on 5-day culture, and addition of ethanol and sodium butyrate on Day 3, followed by cultivation for an additional period of 2 days. At the end of the cultivation period (5 days), the liquid phase was collected for product analysis. Cells were collected for the determination of gene expression levels and then used in bioconversion using resting cells for another period of 2 days. The liquid phase was measured to determine the output of the target products and the expression levels of the key genes related to the biosynthesis of these compounds. Consequently, co-culture with Alternaria MG1 and addition of Tu-chung bark in the medium efficiently increased Pin, PMG, and PDG production yield in the biosynthesis systems using potato dextrose broth medium and resting cells of Phomopsis sp. XP-8. The key genes related to the biosynthesis of these compounds were significantly upregulated. However, in the majority of cases, the addition of ethanol and sodium butyrate, and ultrasound treatment decreased the production yield of Pin, PMG, and PDG. The change in production yield was not consistently accompanied by a change in gene expression.
机译:为了提高(+)-松脂醇(Pin),(+)-松脂醇单糖苷(PMG)和(+)-松脂醇双糖苷(PDG)的生产产率,进行了多种方法,包括与白藜芦醇生产的Alternaria共培养。 sp。培养开始时在培养基中添加MG1孢子并添加土-,在5天的培养中进行超声波处理(40 kHZ,10分钟),并在第3天添加乙醇和丁酸钠,然后再培养一段时间2天在培养期结束时(5天),收集液相进行产物分析。收集用于测定基因表达水平的细胞,然后再用静息细胞进行2天的生物转化。测量液相以确定目标产物的输出以及与这些化合物的生物合成有关的关键基因的表达水平。因此,在使用马铃薯葡萄糖肉汤培养基和Phomopsis sp。的静息细胞的生物合成系统中,与Alternaria MG1共培养并在培养基中添加土Tu树皮可有效提高Pin,PMG和PDG的产量。 XP-8。与这些化合物的生物合成有关的关键基因被显着上调。但是,在大多数情况下,添加乙醇和丁酸钠以及超声处理会降低Pin,PMG和PDG的产量。生产产量的变化并不总是伴随基因表达的变化。

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