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Table 1 A functional study of PDAT derived from different species

From: The synchronous TAG production with the growth by the expression of chloroplast transit peptide-fused ScPDAT in Chlamydomonas reinhardtii

Gene Origin Research Conclusion References
CrPDAT Chlamydomonas reinhardtii Utilizing RNA-Seq insert mutants
Artificial microRNA silencing of PDAT
Demonstrating the relevance of the transacylation pathway
CrPDAT possesses acyl hydrolase activities, mediated membrane lipid turnover and degradation
ScPDAT Saccharomyces cerevisiae Lacking the predicted membrane-spanning region of ScPDAT expressed in Pichia pastoris ScPDAT can catalyze a number of transacylation reactions at a low rate [11]
AtPDAT Arabidopsis Exploring role of enzymes in TAG synthesis by RNA interference
Over-expression of AtPDAT in microsomal preparations of roots and leaves
Coexpression of PDAT1 with oleosin
Disruption of SDP1 TAG lipase or PXA1 severely decreases FA turnover, leading to increases in leaf TAG accumulation
The velocity of AtPDAT dependent on acyl composition
Enhancing fatty acid synthesis and diverting fatty acids from membrane lipids to triacylglycerol
Over-expression of PDAT1 enhances the turnover of FAs in leaf lipids
LuPDAT Linum usitatissimum L. Over-expression of LuPDAT genes in yeast and Arabidopsis Certain PDATs have the unique ability to efficiently channel ALA into TAG [16]
MiPDAT Myrmecia incisa Reisigl Over-expression of MiPDAT and increase transcription levels in M. incisa The mechanism is discussed that MiPDAT in this microalgal uses PC to yield TAG [1]