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The chemical reactions and pathways resulting in the formation of oligosaccharides, molecules with between two and (about) 20 monosaccharide residues connected by glycosidic linkages. The chemical reactions and pathways resulting in the formation of disaccharides, sugars composed of two monosaccharide units. The chemical reactions and pathways resulting in the formation of carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y, carried out by individual cells. The chemical reactions and pathways involving trehalose, a disaccharide isomeric with sucrose and obtained from certain lichens and fungi. The chemical reactions and pathways resulting in the formation of trehalose, a disaccharide isomeric with sucrose and obtained from certain lichens and fungi. The chemical reactions and pathways involving glycosides, compounds in which a glycosyl group is substituted into a hydroxyl, thiol or selenol group in another compound. The chemical reactions and pathways involving any disaccharide, sugars composed of two monosaccharide units. The chemical reactions and pathways resulting in the formation of glycosides, compounds in which a glycosyl group is substituted into a hydroxyl, thiol or selenol group in another compound.

View Gene Ontology (GO) Term

GO TERM SUMMARY

Name: trehalose biosynthetic process
Acc: GO:0005992
Aspect: Biological Process
Desc: The chemical reactions and pathways resulting in the formation of trehalose, a disaccharide isomeric with sucrose and obtained from certain lichens and fungi.
Synonyms:
  • trehalose formation
  • trehalose biosynthesis
  • mykose biosynthesis
  • mykose biosynthetic process
  • mycose biosynthetic process
  • trehalose synthesis
  • trehalose anabolism
  • mycose biosynthesis
Proteins in PDR annotated with:
   This term: 51 [Search]
   Term or descendants: 51 [Search]


[geneontology.org]
INTERACTIVE GO GRAPH

GO:0005992 - trehalose biosynthetic process (interactive image map)

YRC Informatics Platform - Version 3.0
Created and Maintained by: Michael Riffle