Hyun, Kyung-A Liang, Xuhui Xu, Yang Kim, Seung-Young Boo, Kyung-Hwan Park, Jin-Soo Chi, Won-Jae Hyun, Chang-Gu 2024-11-07T02:00:50Z 2024-11-07T02:00:50Z 2024-11-06 2024-10 1661-6596 https://pubs.kist.re.kr/handle/201004/150995 The formation of atroposelective biaryl compounds in plants and fungi is well understood; however, polyketide aglycone synthesis and dimerization in bacteria remain unclear. Thus, the biosynthetic gene cluster (BGC) responsible for antibacterial setomimycin production from Streptomyces nojiriensis JCM3382 was examined in comparison with the BGCs of spectomycin, julichromes, lincolnenins, and huanglongmycin. The setomimycin BGC includes post-polyketide synthase (PKS) assembly/cycling enzymes StmD (C-9 ketoreductase), StmE (aromatase), and StmF (thioesterase) as key components. The heterodimeric TcmI-like cyclases StmH and StmK are proposed to aid in forming the setomimycin monomer. In addition, StmI (P-450) is predicted to catalyze the biaryl coupling of two monomeric setomimycin units, with StmM (ferredoxin) specific to the setomimycin BGC. The roles of StmL and StmN, part of the nuclear transport factor 2 (NTF-2)-like protein family and unique to setomimycin BGCs, could particularly interest biochemists and combinatorial biologists. alpha-Glucosidase, a key enzyme in type 2 diabetes, hydrolyzes carbohydrates into glucose, thereby elevating blood glucose levels. This study aimed to assess the alpha-glucosidase inhibitory activity of EtOAc extracts of JCM 3382 and setomimycin. The JCM 3382 EtOAc extract and setomimycin exhibited greater potency than the standard inhibitor, acarbose, with IC50 values of 285.14 +/- 2.04 mu g/mL and 231.26 +/- 0.41 mu M, respectively. Molecular docking demonstrated two hydrogen bonds with maltase-glucoamylase chain A residues Thr205 and Lys480 (binding energy = -6.8 kcal center dot mol(-1)), two pi-pi interactions with Trp406 and Phe450, and one pi-cation interaction with Asp542. Residue-energy analysis highlighted Trp406 and Phe450 as key in setomimycin's binding to maltase-glucoamylase. These findings suggest that setomimycin is a promising candidate for further enzymological research and potential antidiabetic therapy. English Multidisciplinary Digital Publishing Institute (MDPI) Analysis of the Setomimycin Biosynthetic Gene Cluster from Streptomyces nojiriensis JCM3382 and Evaluation of Its α-Glucosidase Inhibitory Activity Using Molecular Docking and Molecular Dynamics Simulations Article 10.3390/ijms251910758 1 International Journal of Molecular Sciences, v.25, no.19 International Journal of Molecular Sciences 25 19 Y scie scopus 001334151600001 2-s2.0-85206283714 Biochemistry & Molecular Biology Chemistry, Multidisciplinary Biochemistry & Molecular Biology Chemistry Article CRYSTAL-STRUCTURE FERREDOXIN ENZYMES alpha-glucosidase inhibitor biaryl polyketides molecular docking molecular dynamics nonaketide setomimycin BGC