2019
DOI: 10.2991/efood.k.191118.001
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Response Surface Modeling for the Enrichment of Gamma‐Aminobutyric Acid with a Minimum Content of Citrinin in Monascus‐Fermented Rice

Abstract: g-Aminobutyric Acid (GABA) is a secondary metabolite produced in Monascus-fermented food. The mycotoxin (citrinin), another major secondary metabolite, is neurotoxic to humans and thus it diminishes the social acceptability of Monascus-Fermented Rice (MFR). The study was aimed to enrich GABA content and to reduce citrinin level in MFR. Plackett-Burman experimental design and response surface methodology was used to optimize a fermentation medium for a high amount of GABA production with less amount of citrinin… Show more

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Cited by 10 publications
(8 citation statements)
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“…In comparison, the content of GABA in MFR (29.9 mg/g) prepared in this study was slightly higher than that of a previous study, in which a GABA content of 24 mg/g was produced by M. purpureus MTCC 369 (Khan et al, 2019), but the monacolin K content in MFR (2.22 mg/g) was lower than that reported 19.81 mg/g by Zhang et al (2018) and 12.9 mg/g by Lu et al (2013). However, the monacolin K content in MFR could be improved by prolonging the first-stage of fermentation with M. anka 20-2, and a higher GABA yield can also be achieved by extending the second-stage of the bioconversion process with L. plantarum 8014.…”
Section: Production Of Bioactive Mfr By Microbial Consortiacontrasting
confidence: 77%
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“…In comparison, the content of GABA in MFR (29.9 mg/g) prepared in this study was slightly higher than that of a previous study, in which a GABA content of 24 mg/g was produced by M. purpureus MTCC 369 (Khan et al, 2019), but the monacolin K content in MFR (2.22 mg/g) was lower than that reported 19.81 mg/g by Zhang et al (2018) and 12.9 mg/g by Lu et al (2013). However, the monacolin K content in MFR could be improved by prolonging the first-stage of fermentation with M. anka 20-2, and a higher GABA yield can also be achieved by extending the second-stage of the bioconversion process with L. plantarum 8014.…”
Section: Production Of Bioactive Mfr By Microbial Consortiacontrasting
confidence: 77%
“…Production of bioactive MFR by microbial consortia. M. anka 20-2 was activated three times in 250 mL shake flasks containing 50 mL malt extract medium, inoculated with 2.5 mL of the spore suspension (1×10 5 spores/mL), and incubated at 28°C for 48 h prior to use as a starter culture for preparation of MFR (Khan et al, 2019). Then 2 mL of starter culture with 1×10 6 spores/mL was fermented in 250 mL shake flasks containing 40 mL fermentation medium for 7 d on a shaker at 28°C, 200 rpm.…”
Section: Methodsmentioning
confidence: 99%
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“…All the fungal cultures used in the study were cultured on potato dextrose agar (PDA) medium at 30 • C for 7 days and then kept at 4 • C. At every 30 days interval, these fungal strains were subcultured (Khan et al, 2019). Except for DMA production under stress condition, all the…”
Section: Fungal Strains Growth Conditions and Solid-state Fermentationmentioning
confidence: 99%
“…For solid-state fermentation, 20 g of presoaked substrate was transferred to a 250 mL conical flask, to which 40 mL of iron restricted water containing different nutrients were added. The pH of the fermented medium was adjusted to 6.0 with 0.1 M HCl or NaOH and autoclaved for 20 min at 121 • C. Further, it was cooled and inoculated with 5 mL of 2-day-old seed cultures (15%, v/v spore suspension in sterile water having 5.7 × 10 3 spores/mL) of respective fungal strain, which then incubated for 14 days at 30 • C and 70% relative humidity (Khan et al, 2019).…”
Section: Research Highlightsmentioning
confidence: 99%