Abstract

BackgroundBacillus subtilis is an all-important Gram-positive bacterium of valuable biotechnological utility that has been widely used to over-produce industrially and pharmaceutically relevant proteins. There are a variety of expression systems in terms of types of transcriptional patterns, among which the auto-inducible and growth-phase-dependent promoters are gaining increasing favor due to their inducer-independent feature, allowing for the potential to industrially scale-up. To expand the applicability of the auto-inducible expression system, a novel auto-regulatory expression system coupled with cell density was constructed and developed in B. subtilis using the quorum-sensing related promoter srfA (PsrfA).ResultsThe promoter of the srf operon was used to construct an expression plasmid with the green fluorescent protein (GFP) downstream of PsrfA. The expression displayed a cell-density-dependent pattern in that GFP had a fairly low expression level at the early exponential stage and was highly expressed at the late exponential as well as the stationary stages. Moreover, the recombinant system had a similar expression pattern in wild-type B. subtilis 168, WB600, and WB800, as well as in B. subtilis 168 derivative strain 1681, with the complete deletion of PsrfA, indicating the excellent compatibility of this system. Noticeably, the expression strength of PsrfA was enhanced by optimizing the −10 and −35 core sequence by substituting both sequences with consensus sequences. Importantly, the expression pattern was successfully developed in an auto-regulatory cell-density coupling system by the simple addition of glucose in which GFP could not be strongly expressed until glucose was depleted, resulting in a greater amount of the GFP product and increased cell density. The expression system was eventually tested by the successful over-production of aminopeptidase to a desired level.ConclusionThe auto-regulatory cell density coupling system that is mediated by PsrfA is a novel expression system that has an expression pattern that is split between cell-growth and over-expression, leading to an increase in cell density and elevating the overall expression levels of heterologously expressed proteins. The broad applicability of this system and inducer-free expression property in B. subtilis facilitate the industrial scale-up and medical applications for the over-production of a variety of desired proteins.

Highlights

  • Bacillus subtilis is an all-important Gram-positive bacterium of valuable biotechnological utility that has been widely used to over-produce industrially and pharmaceutically relevant proteins

  • Expression pattern of green fluorescent protein (GFP) under the control of promoter srfA (PsrfA) in B. subtilis 168 In recent years, several types of expression systems that are free of inducers via a variety of transcriptional patterns have been developed in B. subtilis or other Gram-positive hosts to over-express industrially and pharmaceutically used proteins [13, 15, 16]

  • These results indicate that the transcription of PsrfA occurs in the late growth phase, whereas the activity of the promoter is inhibited in the early stage of cell-growth, permitting celldensity-dependent expression

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Summary

Introduction

Bacillus subtilis is an all-important Gram-positive bacterium of valuable biotechnological utility that has been widely used to over-produce industrially and pharmaceutically relevant proteins. A rod-shaped Gram-positive soil bacterium, has been regarded to be a “generally recognized as safe” (GRAS) microbe that can naturally secrete numerous extracellular proteins These properties make this bacterium to be one of the most popular hosts for naturally producing a variety of enzymes and over-expressing a large number of pharmaceutical and industrial recombinant proteins of interest, such as amylase [1,2,3,4], lipase [5], alkaline PGL [6], and so on. Two strictly inducible systems, the subtilin-regulated expression (SURE) system and the LiaRS-controlled expression system (LIKE), which rely on the regulation of the promoter for the spa-box and the cell envelope stress-responsive liaI promoter, respectively, have been developed for scientific and industrial applications. Both of these protein expression systems are strictly controlled by the addition of lantibiotic subtilin and bacitracin, respectively, after the exponential phase of cell growth, preventing the leakage of transcription under non-inducing conditions [9, 10]

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