Hydrolysis of starch from corn and sorghum using bacterial enzymes (alpha, beta amylase, and pullulanase) for laboratory-scale glucose syrup production


Çanakçı S., Yıldırım F. N., Ceylan E., Beldüz A. O.

V. International Enzyme and Bioprocess Days EBDays 2024 , İzmir, Türkiye, 27 - 29 Ağustos 2024, ss.98

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: İzmir
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.98
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

Enzymes are complex organic molecules found in living cells. Starch is an important carbohydrate stored in plant cells as a storage material for organisms. Starch is hydrolysed into glucose, maltose, and oligosaccharides by enzymes such as α-, β-amylase, and pullulanase.In this study, 18 mesophilic and thermophilic bacterial isolates, isolated and characterized in the Molecular Biology research laboratory of the Department of Biology, Faculty of Science at KTU, were screened to produce α-amylase, βamylase, and pullulanase. For this purpose, hydrolysis tests were first carried out on solid media containing starch and pullulan. Then, the activities of amylase and pullulanase enzymes showing activity in solid media were determined by the DNS method from the isolated bacteria, and two strains with the potential to produce all three enzymes were prioritized. Enzyme characterization studies were carried out on the two strains showing the best enzyme activity, "Bacillus subtilis (Kont) and Bacillus subtilis (KA4)", The reaction products of the amylase enzymes isolated from Bacillus subtilis (Kont) and Bacillus subtilis (KA4) strains were analyzed using TLC. Then, the starch solution prepared for the study on sweetening the corn starch (glucose syrup production) was treated with enzymes. The reducing sugar determination and glucose content of the samples were determined by the spectrophotometric method using DNS. It was determined that the amount of glucose initially present in the medium increased after enzyme treatment. The reaction products were determined by separations using TLC, and then the reaction products were analyzed by HPLC to determine the starch hydrolysis products