Carbohydrates II

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Contents

Monosaccharides

D-glyceraldehyde molecular structure
L-glyceraldehyde molecular structure.
Mirror images of each other.
D-glucose
carbon C1 and C5 approach
Pyranose ring.
α-D-glucopyranose.
β-D-fructofuranose.
D-glucosamine

Disaccharides

2 glucose molecules approach.
1 water molecule is lost
a glycosidic bond is formed.
Maltose shows a α-glycosidic bond
Cellobiose shows a β-glycosidic bond, like sucrose.

Polysaccharides

  • Starch
    • Amylose

Maltose (2 residues of glucose)
We add a 3rd, 4th, 5th and 6th residues.
Activate rotation to observe helical structure
Zoom out and addition of more glucose residues to reach a 30 residues molecule
Look from a polar view.

    • Amylopectin.-

A fragment of amylopectin including 5 glucose residues.
Zoom in to show a Branch point
4 residues at branch point.
By adding to initial structure 25 glucose residues we get a 30 residues amylopectin fragment.
Zoom out to show that branch points are spaced by 24-30 glucose residues.

  • Glycogen.- Structure like amylopectin but with branch points spaced by 8-12 glucose residues.
  • Cellulose.-

See cellulose.

  • Chitin.- A polymer of β-N-acetil-D-glucosamina.

A 3 residues chitin fragment.

  • Hyaluronic acid.- Heteropolysaccharide with alternating residues of β-N-acetil-D-glucosamine and glucuronic acid

Files for 3D printer

Alpha-amylase with flexible amylopectin by Marius Mihasan


Carbohydrates

Drag the structure with the mouse to rotate

References

Proteopedia Page Contributors and Editors (what is this?)

Alejandro Porto, Karsten Theis, Jaime Prilusky

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