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Heterologous expression, characterization, and application of recombinant thermostable α-amylase from Geobacillus sp. DS3 for porous starch production.
Kurniawan, Dina Clarissa; Rohman, Muhammad Saifur; Witasari, Lucia Dhiantika.
Affiliation
  • Kurniawan DC; Biotechnology Study Program, Faculty of Graduate School, Universitas Gadjah Mada, Jl. Teknika Utara, Kocoran, Sleman, D.I. Yogyakarta 55281, Indonesia.
  • Rohman MS; Biotechnology Study Program, Faculty of Graduate School, Universitas Gadjah Mada, Jl. Teknika Utara, Kocoran, Sleman, D.I. Yogyakarta 55281, Indonesia.
  • Witasari LD; Dept. of Agricultural Microbiology, Faculty of Agriculture, Universitas Gadjah Mada, Jl. Flora, Bulaksumur, Sleman, D.I. Yogyakarta 55281, Indonesia.
Biochem Biophys Rep ; 39: 101784, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39113813
ABSTRACT
Novel Geobacillus sp. DS3, isolated from the Sikidang Crater in Dieng, exhibits promising characteristics for industrial applications, particularly in thermostable α-amylase production. Recombinant technology was used to express thermostable α-amylase in E. coli BL21(DE3) to overcome high-temperature production challenges. The study aimed to express, purify, characterize, and explore potential applications of this novel enzyme. The enzyme was successfully expressed in E. coli BL21(DE3) at 18 °C for 20 h with 0.5 mM IPTG induction. Purification with Ni-NTA column yielded 69.23 % from the initial crude enzyme, with a 3.6-fold increase in specific activity. The enzyme has a molecular weight of ±70 kDa (±58 kDa enzyme+11 kDa SUMO protein). It exhibited activity over a wide temperature range (30-90 °C) and pH range (6-8), with optimal activity at 70 °C and pH 6 with great stability at 60 °C. Kinetic analysis revealed Km and Vmax values of 324.03 mg/ml and 36.5 U/mg, respectively, with dextrin as the preferred substrate without cofactor addition. As a metalloenzyme, it showed the best activity in the presence of Ca2+. The enzyme was used for porous starch production and successfully immobilized with chitosan, exhibiting improved thermal stability. After the fourth reuse, the immobilized enzyme maintained 62 % activity compared to the initial immobilization.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biochem Biophys Rep Year: 2024 Document type: Article Affiliation country: Indonesia Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Biochem Biophys Rep Year: 2024 Document type: Article Affiliation country: Indonesia Country of publication: Netherlands