Esterases play an important role in flavor regulation during food fermentation. In this study, a high esterase-producing strain, Monascus purpureus Y146, was used to optimize esterase production via one-factor-at-a-time experiments (OFAT), response surface methodology (RSM), and an artificial neural network with genetic algorithm (ANN-GA) approach. The esterase was partially purified and characterized, and its application in rice wine fermentation was evaluated using HS-SPME-GC-MS. The results showed that the esterase activity of the Y146 strain reached up to 1248.02 U/mL, a 4.68-fold increase over the unoptimized condition, under conditions of 16% seed inoculation, 10 g/L L-arginine addition at 84 h, pH 7, and 8.69 d of fermentation. The partially purified esterase preparation exhibited optimal activity at 30 °C and pH 7, showed enhanced activity in the presence of 2 mM Fe2+, and had an approximate half-life of 9 h. HS-SPME-GC-MS analysis identified ethyl caprate as the only aroma-active compound (OAV > 1) detected in the control group. Following addition of the partially purified esterase preparation, increased diversity and abundance of volatile compounds were observed, with the number of aroma-active compounds increasing from one to six, including ethyl undecanoate, ethyl hexanoate, ethyl palmitate, ethyl linoleate, 1-dodecanol, and 2,4-Di-tert-butylphenol. These findings highlight the potential application of the M. purpureus Y146-derived partially purified esterase preparation in flavor-oriented fermented food systems.
The content of extracellular Monascus pigments (eMPs), which has strong functional activity and stability, was improved by adding glycine in previous research. This study systematically elucidated the effects of different glycine concentrations on Monascus purpureus (M. purpureus) S109 eMPs production at both the membrane physiological level and the molecular level of pigment secretion-related gene expression. By measuring the biomass, fatty acid, relative conductivity, fluorescence intensity of tyrosine and tryptophan, membrane potential and ion concentration, coenzyme content, and eMPs content, it was found that 2 g/L glycine could significantly enhance cell membrane fluidity and permeability, and promote the production of eMPs, with their content increasing from 85.82 U/mL to 384.88 U/mL. Under this condition, apart from the negative regulator MrpigI, and the MrpigH directly involved in yellow pigment synthesis, which were down-regulated, all other genes associated with the pigment biosynthesis pathway were significantly up-regulated. Furthermore, the expression of MrpigL and MrpigP genes involved in pigment secretion was significantly up-regulated by 2.8-fold and 10.9-fold, respectively. This study demonstrates that glycine promotes eMPs secretion through modulation of membrane physiological properties and modulation of secretion-related gene expression.
Sixu Lin, Xue Yang, Junyao Wang et al.· Microbial Cell Factories· 0 citations
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