Abstract

The goal of this study was to develop a cheap and simple medium and to optimize fermentation parameters for fibrinolytic enzyme production by Bacillus subtilis WR350. A low-cost medium containing 35 g/L sucrose, 20 g/L corn steep powder and 2 g/L MgSO4·7H2O was developed via single-factor and orthogonal experiments. A cheap nitrogen source, corn steep powder, was used to replace the soy peptone present in the initial medium. The highest fibrinolytic activity of 5865 U/mL was achieved using the optimized medium in a 100-L fermenter with an aeration rate of 1.0 vvm and an agitation speed of 200 rpm. The resulting enzyme yield was among the highest described in the literature with respect to fibrinolytic activity, as determined by the fibrin plate method. Techno-economic evaluation indicated that the cost of the optimized medium was only 8.5% of the cost of the initial medium, and the total fermentation cost of fibrinolytic enzyme production using the optimized medium was 23.35% of the cost of using the initial medium.

Highlights

  • Cardiovascular diseases are the primary cause of death in human beings

  • Similar results were obtained in a study by Vijayaraghavan et al.[28], where sucrose was identified as the optimal carbon source for fibrinolytic enzyme production by Bacillus sp

  • The results showed that high concentration of sucrose (>35 g/L) exerted a reduced amount of fibrinolytic enzyme production by B. subtilis WR350, which was probably due to substrate inhibition

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Summary

Introduction

Cardiovascular diseases are the primary cause of death in human beings. Cardiovascular diseases, such as acute myocardial infarction, hypertension and stroke are typically attributed to the excessive accumulation of fibrin in blood vessels[1]. In the present study, after medium optimization in shake flasks, the operating conditions, such as agitation speed and aeration rate, were evaluated in a 100-L pilot fermenter[19,20]. Oxygen supply (OS) is recognized as a significant factor for aerobic microbial fermentation[21] Both agitation speed and aeration rate are important parameters for the control of OS and have a significant effect on the aerobic production of some biopolymers, including glycoprotein GP-120 and bacterial cellulose[22]. The low-cost medium and suitable OS developed for fibrinolytic enzyme production by aerobic fermentation of B. subtilis WR350 may facilitate process optimization for the economical production of microbial fibrinolytic enzymes at an industrial scale

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