Process strategies for enhancing recombinant streptokinase production in Lactococcus lactis cultures using P170 expression system

Abstract

The production of recombinant proteins in Lactococcus lactis is often limited by several process and biological constraints. Recombinant gene expression in the P170 system of L. lactis is triggered at a pH below 6.5 by lactic acid accumulation. This work has used static flask, batch bioreactor and chemostat studies to independently investigate various factors affecting production of recombinant streptokinase. These factors are induction strength, complex-nutrient supplementation, specific growth rate and the cellular response to acid-stress termed as acid tolerance response (ATR). In the P170 system, induction strength is mainly a function of lactate concentration. Recombinant protein production is enhanced by increasing induction strength and complex-nutrient supplementation. However, acid-induced cellular stress-response has a deleterious effect on recombinant protein productivity. It is seen that suppression of ATR has the most predominant effect on enhancing recombinant protein productivity. The insights obtained from batch studies were used to investigate fed-batch processes, both during complete development of ATR and during suppression of ATR. During complete ATR-development, a 25-fold enhancement of volumetric productivity was achieved in fed-batch culture, due to a synergistic combination of increased glucose-feed rates and addition of complex-nutrients to the feed. A combination of these factors and ATR-suppression gave rise to nearly 60-fold increase in volumetric productivity in fed-batch culture over batch processes.