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Published on: January 16, 2019
Production of cytotoxic proteins in Escherichia coli: a fermentation process for producing enzymatically active HIV-1
W K Herber1, F J Bailey, C E Carty
1Department of Cellular and Molecular Biology, Merck, Sharp and Dohme Research Laboratories, West Point, PA 19486.
Abstract:
Two fermentation processes for the tryptophan-regulated expression of active HIV protease (HIV-1 prt) in Escherichia coli are described. Since overexpression of HIV-1 prt results in cell death, stringent control of product expression was necessary to attain high enzyme levels. Such control was achieved by separation of growth and production phases in a two-step process or by implementation of nutrient feed in a one-step process. When the two-stage process was used, soluble product was detectable only when induction occurred at low culture density (A550 less than 3.5). Short induction periods of 1-2 h and rapid harvesting were necessary to recover active product. Similar results were obtained when the single-stage process was operated at 37 degrees C; however, cultivation and induction at 28 degrees C resulted in active enzyme formation following induction at increased cell density (A550 = 10).

