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在分批 Hansenula polymorpha 培养中,通过定向的次级基质限制来增加产物的形成。

Increased product formation induced by a directed secondary substrate limitation in a batch Hansenula polymorpha culture.

机构信息

Chair of Biochemical Engineering, RWTH Aachen University, Worringerweg 1, Sammelbau Biologie, 52056 Aachen, Germany.

出版信息

Appl Microbiol Biotechnol. 2010 Mar;86(1):93-101. doi: 10.1007/s00253-009-2285-0. Epub 2009 Oct 27.

Abstract

By the use of directed limitations of secondary substrates, the metabolic flux should be deflected from biomass production to product formation. In order to study the impact of directed limitations caused by various secondary substrates on the growth and product formation of the methylotrophic yeast Hansenula polymorpha, the cultivation systems respiration activity monitoring system (RAMOS) and BioLector were used in parallel. While the RAMOS device allows the online monitoring of the oxygen transfer rate in shake flasks, the BioLector enables in microtiter plates the monitoring of scattered light and the fluorescence intensity of the green fluorescent protein (GFP). Secondary substrate limitations of phosphate, potassium, and magnesium were analyzed in batch fermentations. The sole carbon source was either 10 g/L glucose or 10 g/L glycerol. The expression of the GFP gene is controlled by the FMD promoter (formate dehydrogenase). In batch cultures with glucose as carbon source, a directed limitation of phosphate increased the GFP production 1.87-fold, compared to phosphate unlimited conditions. Under potassium-limited conditions with glycerol as sole carbon source, the GFP production was 1.41-fold higher compared to unlimited conditions. A limitation of the substrate magnesium resulted in a 1.22-fold increase GFP formation in the case of glycerol as carbon source.

摘要

通过对次级底物的定向限制,可以将代谢通量从生物量生产转向产物形成。为了研究各种次级底物的定向限制对甲醇营养酵母汉逊德巴利酵母生长和产物形成的影响,平行使用了培养系统呼吸活性监测系统 (RAMOS) 和 BioLector。虽然 RAMOS 设备允许在线监测摇瓶中的氧传递速率,但 BioLector 可以在微孔板中监测散射光和绿色荧光蛋白 (GFP) 的荧光强度。在分批发酵中分析了磷酸盐、钾盐和镁盐的次级底物限制。唯一的碳源是 10 g/L 葡萄糖或 10 g/L 甘油。GFP 基因的表达受 FMD 启动子(甲酸脱氢酶)的控制。在以葡萄糖为碳源的分批培养中,与无磷酸盐限制条件相比,磷酸盐的定向限制使 GFP 产量增加了 1.87 倍。在以甘油为唯一碳源的钾盐限制条件下,与无限制条件相比,GFP 产量增加了 1.41 倍。在以甘油为碳源的情况下,底物镁盐的限制导致 GFP 形成增加了 1.22 倍。

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