The reducing sugar content was determined using the 3,5-dinitrosalicylic acid (DNS) method.52 The supernatant (1 mL) of culture, collected during fermentation, was mixed with 1 mL of DNS reagent and then heated at 100 °C for 15 min. The absorbance was monitored at 540 nm by an ultraviolet–visible (UV–vis) spectrometer. The content of reducing sugars was determined by comparing it to a standard curve created by glucose at different concentrations.
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