Functional characterization of front-end desaturases from trypanosomatids depicts the first polyunsaturated fatty acid biosynthetic pathway from a parasitic protozoan

TRIPODI, KARINA; BUTTIGLIERO, L.; ALTABE, S.; UTTARO, A. D.

The Febs Journal

Año: 2006 vol. 273 p. 271 - 280

A survey of the three kinetoplastid genome projects revealed the presence of three putative front-end desaturase genes in Leishmania major, one inLeishmania major, one in Trypanosoma brucei and two highly identical ones (98%) in T. cruzi. The encoded gene products were tentatively annotated as D8, D5 and D6 desaturases for L. major, and D6 desaturase for both trypanosomes. After phylogenetic and structural analysis of the deduced proteins, we predicted that the putative D6 desaturases could have D4 desaturase activity, based mainly on the conserved HX3HH motif for the second histidine box, when compared with D4 desaturases from Thraustochytrium,and two highly identical ones (98%) in T. cruzi. The encoded gene products were tentatively annotated as D8, D5 and D6 desaturases for L. major, and D6 desaturase for both trypanosomes. After phylogenetic and structural analysis of the deduced proteins, we predicted that the putative D6 desaturases could have D4 desaturase activity, based mainly on the conserved HX3HH motif for the second histidine box, when compared with D4 desaturases from Thraustochytrium,D8, D5 and D6 desaturases for L. major, and D6 desaturase for both trypanosomes. After phylogenetic and structural analysis of the deduced proteins, we predicted that the putative D6 desaturases could have D4 desaturase activity, based mainly on the conserved HX3HH motif for the second histidine box, when compared with D4 desaturases from Thraustochytrium,L. major, and D6 desaturase for both trypanosomes. After phylogenetic and structural analysis of the deduced proteins, we predicted that the putative D6 desaturases could have D4 desaturase activity, based mainly on the conserved HX3HH motif for the second histidine box, when compared with D4 desaturases from Thraustochytrium,D6 desaturases could have D4 desaturase activity, based mainly on the conserved HX3HH motif for the second histidine box, when compared with D4 desaturases from Thraustochytrium,3HH motif for the second histidine box, when compared with D4 desaturases from Thraustochytrium,D4 desaturases from Thraustochytrium, Euglena gracilis and the microalga, Pavlova lutheri, which are more than 30% identical to the trypanosomatid enzymes. After cloning and expression in Saccharomyces cerevisiae, it was possible to functionally characterize each of the front-end desaturases present in L. major andand the microalga, Pavlova lutheri, which are more than 30% identical to the trypanosomatid enzymes. After cloning and expression in Saccharomyces cerevisiae, it was possible to functionally characterize each of the front-end desaturases present in L. major andSaccharomyces cerevisiae, it was possible to functionally characterize each of the front-end desaturases present in L. major andL. major and T. brucei. Our prediction about the presence of D4 desaturase activity in the three kinetoplastids was corroborated. In the same way, D5 desaturase activity was confirmed to be present in L. major. Interestingly, the putative D8 desaturase turned out to be a functional D6 desaturase, being 35% and 31% identical to Rhizopus oryzae and Pythium irregulare. Our prediction about the presence of D4 desaturase activity in the three kinetoplastids was corroborated. In the same way, D5 desaturase activity was confirmed to be present in L. major. Interestingly, the putative D8 desaturase turned out to be a functional D6 desaturase, being 35% and 31% identical to Rhizopus oryzae and Pythium irregulareD5 desaturase activity was confirmed to be present in L. major. Interestingly, the putative D8 desaturase turned out to be a functional D6 desaturase, being 35% and 31% identical to Rhizopus oryzae and Pythium irregulareL. major. Interestingly, the putative D8 desaturase turned out to be a functional D6 desaturase, being 35% and 31% identical to Rhizopus oryzae and Pythium irregulareD8 desaturase turned out to be a functional D6 desaturase, being 35% and 31% identical to Rhizopus oryzae and Pythium irregulareRhizopus oryzae and Pythium irregulare D6 desaturases, respectively. Our results indicate that no conclusive predictions can be made about the function of this class of enzymes merely on the basis of sequence homology. Moreover, they indicate that a complete pathway for very-long-chain polyunsaturated fatty acid biosynthesis is functional in L. major using D6, D5 and D4 desaturases. In trypanosomes, only D4 desaturases are present. The putative algal origin of the pathway in kinetoplastids is discussed.6 desaturases, respectively. Our results indicate that no conclusive predictions can be made about the function of this class of enzymes merely on the basis of sequence homology. Moreover, they indicate that a complete pathway for very-long-chain polyunsaturated fatty acid biosynthesis is functional in L. major using D6, D5 and D4 desaturases. In trypanosomes, only D4 desaturases are present. The putative algal origin of the pathway in kinetoplastids is discussed.L. major using D6, D5 and D4 desaturases. In trypanosomes, only D4 desaturases are present. The putative algal origin of the pathway in kinetoplastids is discussed.D4 desaturases are present. The putative algal origin of the pathway in kinetoplastids is discussed.