Construction of an engineered for production of poly-γ-glutamic acids with specific molecular weights.

INTRODUCTION

Poly-γ-glutamic acid (γ-PGA) with different molecular weight (Mw) exhibits different properties and therefore has a variety of applications. At present, the γ-PGA is mainly produced by species. However, the production of γ-PGAs with specific Mws often requires multiple strains, which limits the development and application of γ-PGA.

METHODS

To address this limitation, we constructed an engineered strain by deleting hydrolase genes , and , and further introduced regulation of PgdS expression under an IPTG-inducible promoter.

RESULTS

When the hydrolase genes , and in were deleted, the γ-PGA Mw and titer increased by 220.1% (2.42×10 Da) and 47.81% (8.44 g/L), respectively. Furthermore, regulation of PgdS expression enabled dynamic control of γ-PGA Mw. The γ-PGA with Mw ranging from 9.55×10 Da to 2.15×10 Da was produced by change of IPTG addition time in an engineered strain, with the titer of 6.28-8.57 g/L. In the 5-L fermenter, the γ-PGA with Mw ranging from 8.3×10 Da to 1.87×10 Da was produced under optimal conditions.

CONCLUSION

In summary, an engineered strain that can dynamically regulate the γ-PGA Mw and produce γ-PGAs with specific Mws was obtained, and its regulatory range was wider than that of previous studies, which increased the application potential.