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由香草酸刺激的云芝漆酶产量的扩大化生产。

Scale-up laccase production from Trametes versicolor stimulated by vanillic acid.

作者信息

Wang Ke-Feng, Hu Jian-Hua, Guo Chen, Liu Chun-Zhao

机构信息

National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, 100190, People's Republic of China.

University of Chinese Academy of Sciences, Beijing, 100049, People's Republic of China.

出版信息

Bioprocess Biosyst Eng. 2016 Jul;39(7):1041-9. doi: 10.1007/s00449-016-1582-0. Epub 2016 Mar 14.

Abstract

An efficient strategy for laccase production in Trametes versicolor cultures was developed using vanillic acid as the inducer. The optimized vanillic acid treatment strategy consisted of exposing 2-day-old mycelia cultures to 80 mg/L vanillic acid. After 4 days, laccase activity of 588.84 U/L was achieved in flasks which represented a 1.79-fold increase compared to the control. In 200-L airlift bioreactor, the maximal laccase activity reached up to 785.12 U/L using the optimized vanillic acid treatment strategy. The zymograms of culture supernatants revealed three bands with laccase activity, among which Lac1 and Lac2 were abundant laccase isoforms constitutively expressed, and Lac3 was an inducible isozyme by vanillic acid. The results of real-time quantitative PCR showed that the transcription level of lcc in T. versicolor cultures grown with vanillic acid for 7 days was about 5.64-fold greater than that without vanillic acid in flasks. In 200-L airlift bioreactor cultures of T. versicolor with addition of vanillic acid, the transcript level of lcc at day 7 was 2.62-fold higher than that in flasks with vanillic acid due to the good mass transfer and oxygen supply in the bioreactor system. This study provides a basis for understanding the induction mechanism of vanillic acid for laccase production and has good potential for industrial applications.

摘要

以香草酸为诱导剂,开发了一种在云芝培养物中高效生产漆酶的策略。优化后的香草酸处理策略包括将2日龄的菌丝体培养物暴露于80mg/L的香草酸中。4天后,摇瓶中的漆酶活性达到588.84U/L,与对照相比提高了1.79倍。在200L气升式生物反应器中,采用优化后的香草酸处理策略,漆酶的最大活性达到785.12U/L。培养上清液的酶谱显示有三条具有漆酶活性的条带,其中Lac1和Lac2是组成型表达的丰富漆酶同工型,Lac3是香草酸诱导的同工酶。实时定量PCR结果表明,在摇瓶中用香草酸培养7天的云芝培养物中,lcc的转录水平比不用香草酸培养的培养物高约5.64倍。在添加香草酸的200L气升式生物反应器云芝培养物中,由于生物反应器系统良好的传质和供氧,第7天lcc的转录水平比摇瓶中添加香草酸的培养物高2.62倍。本研究为理解香草酸对漆酶产生的诱导机制提供了依据,具有良好的工业应用潜力。

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