Related Experiment Video
Updated: Sep 12, 2026

Structural Biology and Analytical Chemistry Approaches for Characterizing C-Glycoside Metabolic Enzymes in Human Gut Microbiota
Published on: May 23, 2025
Structural and Functional Perspectives of α-L-Rhamnosidase in Glycoside Biotransformation, Therapeutic Applications,
Kunwar Vishal1, Vinita Yadav1, Pramod K Yadav1
1Department of Life Sciences and Biotechnology, Chhatrapati Shahu Ji Maharaj University, Kanpur, Uttar Pradesh208024, India.
Abstract:
α-L-Rhamnosidase is a glycoside hydrolase (GH) that cleaves α-L-rhamnosidic bonds in diverse natural substrates, including oligosaccharides, glycoproteins, flavonoids, and glycolipids that contain terminal L-rhamnose. Owing to its broad substrate specificity, it has attracted growing interest in biotechnology, food processing, pharmaceuticals, and natural product modification. Fungal and bacterial α-L-rhamnosidases show diversity in molecular architecture, catalytic efficiency, thermostability, and pH tolerance, while sharing a conserved inverting mechanism mediated by acidic residues within the GH78 and GH106 families. Structural studies reveal catalytic cores, substrate recognition motifs, and aromatic residues involved in rhamnose binding. These enzymes enable the production of bioactive compounds such as prunin, isoquercitrin, quercetin, hesperetin, icariin, and myricetin. Recent advances in computational design, protein engineering, and directed evolution have improved enzyme performance. This review summarizes the current knowledge of microbial α-L-rhamnosidases, emphasizing their sources, biochemical characteristics, substrate specificity, structural organization, catalytic mechanisms, therapeutic relevance, and recent advances in protein engineering.
Related Concept Videos
Enzymes
Enzyme deficiencies can often translate into life-threatening diseases. For example, a genetic abnormality resulting in the deficiency of the enzyme G6PD...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Structure-Activity Relationships and Drug Design
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...
Ligand Binding and Linkage
Allosteric Proteins-ATCase
Aspartate transcarbamoylase (ATCase) is a cytosolic enzyme that catalyzes the condensation of L-aspartate and carbamoyl phosphate to N-carbamoyl-L-aspartate. This reaction is the first step in pyrimidine biosynthesis. UTP and CTP, the end products of the pyrimidine synthesis pathway,...
Enzyme Inhibition
