Abstract

In this study, an efficient strategy of high-cell-density cultivation was exploited to obtain recombinant l-glutamate oxidase (LGOX), which was used to produce alpha-ketoglutaric acid (α-KG) from l-glutamic acid. First, lactose was used to replace isopropyl β-D-1-thiogalactopyranoside as a cheaper and more effective inducer. Second, a novel, two-stage feeding strategy was proposed, in which the exponential feeding mode was first performed in a 5-L fermenter until the maximum dissolved oxygen (DO) concentration was reached, which was followed by a DO-stat feeding mode. Based on the two-stage feeding strategy and by optimizing the induction strategies, the maximal cell density and LGOX activity reached 48.4g/L and 156.1U/mL, respectively, after 20h of cultivation. When a whole-cell biocatalyst was used, the titer of α-KG was up to 127.2g/L from 132g/L l-glutamic acid in 24h.

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