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里氏木霉在乳糖培养基上采用计算机控制补料策略进行连续培养时高效生产纤维素酶。

Efficient cellulase production by Trichoderma reesei in continuous cultivation on lactose medium with a computer-controlled feeding strategy.

作者信息

Bailey M J, Tähtiharju J

机构信息

VTT Biotechnology, Tietotie 2, Box 1500, 02044 VTT, Espoo, Finland.

出版信息

Appl Microbiol Biotechnol. 2003 Aug;62(2-3):156-62. doi: 10.1007/s00253-003-1276-9. Epub 2003 Apr 3.

Abstract

A low-foaming hydrophobin II deletant of the Trichoderma reesei strain Rut-C30 was used for production of cellulases by continuous cultivation on lactose medium in a laboratory fermenter. The control paradigm of the addition of new medium to the continuous process was based on the growth dynamics of the fungus. A decrease in the rate of base addition to the cultivation for pH-minimum control was used as an indicator of imminent exhaustion of carbon source for growth and enzyme induction. When the amount of base added per 5 min computation cycle decreased below a given value, new medium was added to the fermenter. When base addition for pH control thereafter increased above the criterion value, due to increased growth, the medium feed was discontinued or decreased. The medium feeding protocol employed was successful in locking the fungus in the stage of imminent, but not actual, exhaustion of carbon source. According to the results of a batch cultivation of the same strain on the same medium, this is the phase of maximal enzyme productivity. The medium addition protocol used in this work resulted in a very stable continuous process, in which cellulase productivity was maintained for several hundred hours at the maximum level observed in a batch cultivation for only about 10 h. Despite a major technical disturbance after about 420 h, the process was restored to stability. When the cultivation was terminated after 650 h, the level of enzyme production was still maximal, with no signs of instability of the process.

摘要

里氏木霉Rut-C30菌株的一种低泡沫疏水蛋白II缺失体用于在实验室发酵罐中以乳糖培养基连续培养生产纤维素酶。向连续过程中添加新培养基的控制模式基于真菌的生长动态。将用于pH最低控制的培养过程中碱添加速率的降低用作生长和酶诱导的碳源即将耗尽的指标。当每5分钟计算周期添加的碱量降至给定值以下时,向发酵罐中添加新培养基。此后,由于生长增加,用于pH控制的碱添加量增加到标准值以上时,培养基进料停止或减少。所采用的培养基进料方案成功地将真菌锁定在碳源即将耗尽但尚未实际耗尽的阶段。根据同一菌株在同一培养基上的分批培养结果,这是酶生产率最高的阶段。本研究中使用的培养基添加方案产生了非常稳定的连续过程,其中纤维素酶生产率在分批培养中仅约10小时观察到的最高水平下维持了数百小时。尽管在约420小时后发生了重大技术干扰,但该过程恢复了稳定性。当在650小时后终止培养时,酶产生水平仍然最高,没有过程不稳定的迹象。

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