首页> 外文期刊>Biotechnology Journal: Healthcare,Nutrition,Technology >A microwell platform for the scale-up of a multistep bioconversion to bench-scale reactors: Sitosterol side-chain cleavage
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A microwell platform for the scale-up of a multistep bioconversion to bench-scale reactors: Sitosterol side-chain cleavage

机译:用于将多步生物转化规模扩大到台式规模反应器的微孔平台:谷甾醇侧链裂解

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摘要

The microwell-scale approach is widely used for screening purposes and one-pot biotransformations, but it has seldom been applied to complex whole cell multistep bioconversions, requiring prolonged incubation periods. The present study aims to contribute to filling this gap. The side-chain cleavage of sitosterol to androstenedione (AD) with Mycobacterium sp. NRRL B-3805 cells was used as a model system, and focus was given to the screening of suitable bioconversion media with 24-well microwell plates. Results show that to perform this particular bioconversion growing cells are preferred over resting cells due to higher conversion yields obtained in aqueous medium. The use of resting cells may nevertheless present an interesting approach provided catalytic activity is retained throughout successive runs. Maintaining suitable aeration levels (air flow of 1 mL/min) allowed minimizing the decay of catalytic activity typically observed alongside consecutive bioconversion runs with resting cells. Microwell plates with dedicated oxygen and pH monitoring capabilities proved effective in media development for complex multistep bioconversions using relatively slow-growing bacteria. Under constant k_La (0.044/s) similar AD production and dissolved oxygen profiles were observed in microwell plates and in a bench-scale reactor. Selection of a suitable k_La value proved critical, since under lower k_La values scale-up proved unsuccessful. The same pattern was observed when other scale-up criteria were evaluated to perform the scale-up of this particular bioconversion. Results gathered seem to validate the proposed approach "from microwell plate to bench-scale fermentor".
机译:微孔规模的方法被广泛用于筛选和一锅法生物转化,但很少用于复杂的全细胞多步生物转化,需要延长孵育时间。本研究旨在为填补这一空白做出贡献。用分枝杆菌属物种将谷固醇侧链裂解为雄烯二酮(AD)。 NRRL B-3805细胞用作模型系统,重点是用24孔微孔板筛选合适的生物转化培养基。结果表明,由于在水性培养基中获得较高的转化率,因此与静息细胞相比,进行这种特定的生物转化生长细胞更为可取。如果在整个连续运行中都保持催化活性,则使用静息细胞可能仍然是一种有趣的方法。维持合适的通气水平(1 mL / min的空气流量)可以使催化活性的衰减最小化,通常伴随着静止细胞进行的连续生物转化过程中观察到的。具有专用的氧气和pH监测功能的微孔板在使用相对缓慢生长的细菌进行复杂的多步生物转化的培养基开发中证明是有效的。在常数k_La(0.044 / s)下,在微孔板和台式反应器中观察到相似的AD产生和溶解氧分布。选择合适的k_La值被证明是至关重要的,因为在较低的k_La值下,放大失败了。当评估其他放大标准以执行该特定生物转化的放大时,观察到相同的模式。收集的结果似乎验证了所提出的方法“从微孔板到台式发酵罐”。

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