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Table 1 Properties of promoters used for β-CGTase expression optimization

From: High-level extracellular protein production in Bacillus subtilis using an optimized dual-promoter expression system

Promoter

Origin

Properties

Expression reporter proteins

Psrf

B. subtilis

Auto-inducible system regulated by ComA–ComP phosphorylation system [14]

Green florescent protein, aminopeptidase

Pxyl′

B. subtilis

Xylose-based expression system and catabolite repressed by catabolite-responsive element [11]

β-Galactosidase, glycerol-3-phosphate cytidylyltransferase

PgsiB

B. subtilis

Subject to σB regulation and is induced by ethanol, heat and acid shock [30]

β-Galactosidase [50]

Pxyl

B. megaterium

Xylose-based expression system and glucose repression [10]

β-Galactosidase and other heterologous proteins

PHpaII

Staphylococcus aureus

Strong constitutive promoter that stimulates counterclockwise RNA synthesis [13]

β-Galactosidase, chloramphenicol acetyltransferase and other heterologous proteins

PamyQ′

B. subtilis

Regulated by the DegS–DegU two-component system [32]

β-Galactosidase

PaprE

B. subtilis

Promoter of alkaline protease

None

PnprE

B. subtilis

Promoter of neutral protease

None