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Biosynthesis of Polysaccharides01:26

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Polysaccharides such as glycogen and starch are synthesized from nucleoside diphosphate sugars, primarily uridine diphosphate glucose (UDPG) and adenosine diphosphate glucose (ADPG). These activated glucose donors act as key intermediates in carbohydrate metabolism and biosynthesis. UDPG primarily involves glycogen synthesis in animals and many bacteria, while ADPG plays a fundamental role in starch synthesis in plants and certain bacteria.UDPG is formed when glucose-1-phosphate reacts with...
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Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
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Glycosylation, the most common post-translational modification for proteins, serves diverse functions. Adding sugars to proteins makes the proteins more resistant to proteolytic digestion. Glycosylated proteins can act as markers and receptors to promote cell-cell adhesion. Additionally, they have many essential quality control functions in the cell, such as correct protein folding and facilitating transport of misfolded proteins to the cytosol, which can be degraded.
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Cyclodextrin glucanotransferase: fundamentals and biotechnological implications.

Dimple S Pardhi1, Khushbu J Rabadiya1, Rakeshkumar R Panchal1

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Cyclodextrin glucanotransferase (CGTase) enzymes transform starches into cyclodextrins via transglycosylation. This review compiles bacterial CGTase sources, properties, and cyclodextrin applications in various industries.

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Area of Science:

  • Enzymology and Biotechnology
  • Microbial Biochemistry

Background:

  • Cyclodextrin glucanotransferase (CGTase) is a GH13 α-amylase family enzyme.
  • CGTase catalyzes cyclization, coupling, disproportionation, and hydrolysis of α-1,4-glucans.
  • Cyclodextrins form inclusion complexes, finding broad industrial applications.

Purpose of the Study:

  • To compile bacterial sources, biochemical properties, production conditions, and structures of CGTases.
  • To review CGTase production by Bacillus spp. and other bacterial genera.
  • To provide insights into cyclodextrin properties and biotechnological applications.

Main Methods:

  • Literature review of CGTase and cyclodextrin research.
  • Compilation of data on bacterial CGTase producers, focusing on Bacillus spp.
  • Analysis of CGTase biochemical properties and production parameters.

Main Results:

  • Bacillus genus accounts for ~90% of CGTase producers.
  • Alkaliphilic bacteria under submerged fermentation are optimal for CGTase production.
  • CGTases exhibit five distinct domains (A-E) with variable structures.

Conclusions:

  • CGTase is a versatile enzyme with significant biotechnological potential.
  • Diverse bacterial genera contribute to CGTase production, with Bacillus spp. being predominant.
  • Cyclodextrins offer unique properties for applications in food, pharmaceuticals, and chemical industries.