Lipoxygenases are a group of non-heme iron containing dioxygenases catalyzing the addition of molecular oxygen to poly unsaturated fatty acids in a stereospecific as well as regiospecific way and involved in the biosynthesis of inflammatory mediators, in cell differentiation and atherogenesis. Synthetic use of lipoxygenase over the last decade for total synthesis of several natural products, e.g. 6(R)-lopoxin A, 5(S)-HPETE, (R) and (S) coriolide is discussed in this review. In the second part of the review we have discussed on the LOX biocatalysis of unnatural substrates mimicking natural substrates, lipoxygenase biocatalysis in non-conventional media, the use of immobilized LOX and biocatalysis with engineered lipoxygenase. The factors governing the regiospecificity as well as stereospecificity of LOX biocatalysis will also be discussed here. From the synthetic chemist’s point of view, the asymmetric oxygenation reaction of unnatural substrates has a tremendous potential. The products of these reactions are important chiral building blocks for the total synthesis of numerous biological active natural products.
Source: Journal of Molecular Catalysis B: Enzymatic (2003) vol. 26, p. 3-28
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