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Home >> Industrial and Microbial Biotechnology >> Biocatalysis and Enzyme Biotechnology >>Biotransformation of Polyunsaturated Fatty Acids (PUFAs)

Biotransformation of Polyunsaturated Fatty Acids (PUFAs)
An interesting area of biotechnology research is to obtain polyunsaturated fatty acids (PUFAs) and utilize them either directly or for their biotransformation to other bioactive compounds. Some of the PUFAs are listed in Table.

Different polyunsaturated fatty acids and their nomenclature

Fatty Acid (PUFA)

PUFA nomenclature

m:n (w--x)

m:naz,….nz

Arachidonic Acid (AA)

20:4 (ω-6)

20:4 5z, 8z, 11z, 14z

a-Linolenic acid (ALA)

18:3 (ω-3)

18:3 9z, 12z, 15z

Docosahexaenoic aicd (DHA)

22:6 (ω-3)

22:6 4z, 7z, 10z, 13z, 16z,z19z

Dihomo-g-linolenic acid (DHGLA)

20:3 (ω-6)

20:3 8z, 11z, 14z

Docosapentaenoic acid (DPA)

22:5 (ω-3)

22:57z, 10z, 13z, 16z, 19z

Eicosapentaenoic acid (EPA)

20:5 (ω-3)

20:55z, 8z, 11z, 14z, 17z

Eicosatrienoic acid (ETA)

20:3 (ω-6)

20:35z, 11z, 14z

Eicosatetraenoic acid (ETRA)

20:4 (ω-3)

20:45z, 11z, 14z, 17z

g-Linolenic acid (GLA)

18:3 (ω-6)

18:36z, 9z, 12z

Linoleic acid (LA)

18:2 (ω-6)

18:29z, 12z

Note:In m:n(ω--x)and m:naz..nz, m and n refer to number of carbon atoms and the double bonds, (ω -x) refers to position, where the final double bond is located, x-carbon atoms (inclusive) away from the terminal carbon atom(ω); in the superscrips az to nz, a and n indicate the positions of double bonds (carbon atoms numbered from carboxyl end).

The biotransformations of PUFAs include two major classes of reactions: (i) Hydrolase-mediated reactions, where PUFA remains unaffected, but overall lipid structure is altered to provide products with desirable nutritional, biomedical or surfactant attributes, (ii) Oxidative transformations, which yield molecules with biological activities of relevance to flavour, pharmaceuticals and fine chemical industries.

 

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