Abstract
A highly sensitive ethanol biosensor based on Acetobacter aceti biofilm, which contains pyrroloquinoline quinone-alcohol dehydrogenase enzyme for halal detection in food and beverages, has been developed. In this study, A. aceti cells were purified by determining the conditions of growth time, incubation temperature, and pH to suppress the yeast growth. Selection of optimum conditions for biofilm formation was also carried out to obtain a stable sensor operation. The optimum biofilm formation was 14 days. The performance of biosensor was investigated by the cyclic voltammetry technique. Linear range, sensitivity, limit of detection (LOD), and limit of quantification (LOQ) were found to be 5 × 10−5–3 × 10−4 %, 43,076 µA %−1, 2.32 × 10−5, and 7.03 × 10−5 %, respectively. The repeatability of biosensor was tested in 1 × 10−5 − 1% ethanol concentration and the relative standard deviation was 1.08% (for n = 7). The stability studies have shown that the cyclic voltammetry response of biosensor to ethanol leave the act of 98.99% at the 7 week. Thus, the developed biosensor is promising to be used for simple analysis of halal products and has been tested on real sample.
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CITATION STYLE
Susparini, N. T., Abidin, Z., Iswantini, D., & Nurhidayat, N. (2019). Sensitive and stable ethanol biosensor development based on acetobacter aceti biofilm for halal detection of food and beverages. Journal of Applied Biology and Biotechnology, 7(6), 40–47. https://doi.org/10.7324/JABB.2019.70607
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