4.7 Article

LIP4 Is Involved in Triacylglycerol Degradation in Chlamydomonas reinhardtii

期刊

PLANT AND CELL PHYSIOLOGY
卷 60, 期 6, 页码 1250-1259

出版社

OXFORD UNIV PRESS
DOI: 10.1093/pcp/pcz037

关键词

Chlamydomonas reinhardtii; Lipid catabolism; N resupply; SUGAR DEPENDENT1; Triacylglycerol degradation; Triacylglycerol lipase

资金

  1. Thailand Research Fund [MRG6080038]
  2. Faculty of Science, Kasetsart University [PRF-PII 60 P2 60]
  3. Division of Chemical Sciences, Geosciences and Biosciences, Office of Basic Energy Sciences of the United States Department of Energy [DE-FG02-91ER20021]
  4. MSU AgBioResearch
  5. Royal Thai Government Scholarship
  6. Embassy of France in Thailand

向作者/读者索取更多资源

Degradation of the storage compound triacylglycerol ( TAG) is a crucial process in response to environmental stimuli. In microalgae, this process is important for re-growth when conditions become favorable after cells have experienced stresses. Mobilization of TAG is initiated by actions of lipases causing the release of glycerol and free fatty acids, which can be further broken down for energy production or recycled to synthesize membrane lipids. Although key enzymes in the process, TAG lipases remain to be characterized in the model green alga Chlamydomonas reinhardtii. Here, we describe the functional analysis of a putative TAG lipase, i. e. LIP4, which shares 44% amino acid identity with the major TAG lipase in Arabidopsis ( SUGAR DEPENDENT1-SDP1). The LIP4 transcript level was down-regulated during nitrogen deprivation when TAG accumulates, but was upregulated during nitrogen resupply ( NR) when TAG was degraded. Both artificial microRNA and insertional mutants showed a delay in TAG mobilization during NR. The difference in TAG degradation was more pronounced when the cultures were incubated without acetate in the dark. Furthermore, the lip4 insertional mutants over-accumulated TAG during optimal growth conditions. Taken together, the results suggest to us that LIP4 likely acts as a TAG lipase and plays a role in TAG homeostasis in Chlamydomonas.

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