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| in the current study, a glyA gene from the marine bacteriumAlcanivorax sp.was cloned and expressed in E. coli, and then the recombinant AdSHMT enzyme was purified and characterized. Additionally, the correlation of the AdSHMT enzyme production and activity with the fermentation time of recombinant E. coli was investigated. The molecular conversion rate of AdSHMT in l-serine enzymatic production was also evaluated. |
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