4.8 Article

Physaria fendleri and Ricinus communis lecithin:cholesterol acyltransferase-like phospholipases selectively cleave hydroxy acyl chains from phosphatidylcholine

Journal

PLANT JOURNAL
Volume 105, Issue 1, Pages 182-196

Publisher

WILEY
DOI: 10.1111/tpj.15050

Keywords

phospholipase A; lecithin:cholesterol acyltransferase-like PLA; hydroxy fatty acid; phosphatidylcholine; triacylglycerol; Physaria fendleri; Ricinus communis; Arabidopsis thaliana

Categories

Funding

  1. Canada Research Chairs Program
  2. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN-2016-05926, RGPIN-2014-04585]
  3. Alberta Innovates
  4. Alberta Agriculture and Forestry
  5. University of Alberta Start-up Research Grant
  6. National Natural Science Foundation of China [31371661]
  7. Canadian Foundation for Innovation and Research Capacity Program of Alberta Enterprise and Advanced Education

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This study revealed the role of LCAT-PLAs in HFA biosynthesis in transgenic crops, demonstrating that PfLCAT-PLA and RcLCAT-PLA can enhance the accumulation of HFAs at the sn-1/3 positions of TAG.
Production of hydroxy fatty acids (HFAs) in transgenic crops represents a promising strategy to meet our demands for specialized plant oils with industrial applications. The expression of Ricinus communis (castor) OLEATE 12-HYDROXYLASE (RcFAH12) in Arabidopsis has resulted in only limited accumulation of HFAs in seeds, which probably results from inefficient transfer of HFAs from their site of synthesis (phosphatidylcholine; PC) to triacylglycerol (TAG), especially at the sn-1/3 positions of TAG. Phospholipase As (PLAs) may be directly involved in the liberation of HFAs from PC, but the functions of their over-expression in HFA accumulation and distribution at TAG in transgenic plants have not been well studied. In this work, the functions of lecithin:cholesterol acyltransferase-like PLAs (LCAT-PLAs) in HFA biosynthesis were characterized. The LCAT-PLAs were shown to exhibit homology to LCAT and mammalian lysosomal PLA(2), and to contain a conserved and functional Ser/His/Asp catalytic triad. In vitro assays revealed that LCAT-PLAs from the HFA-accumulating plant species Physaria fendleri (PfLCAT-PLA) and castor (RcLCAT-PLA) could cleave acyl chains at both the sn-1 and sn-2 positions of PC, and displayed substrate selectivity towards sn-2-ricinoleoyl-PC over sn-2-oleoyl-PC. Furthermore, co-expression of RcFAH12 with PfLCAT-PLA or RcLCAT-PLA, but not Arabidopsis AtLCAT-PLA, resulted in increased occupation of HFA at the sn-1/3 positions of TAG as well as small but insignificant increases in HFA levels in Arabidopsis seeds compared with RcFAH12 expression alone. Therefore, PfLCAT-PLA and RcLCAT-PLA may contribute to HFA turnover on PC, and represent potential candidates for engineering the production of unusual fatty acids in crops.

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