
Enhancement of extraplastidic oil synthesis in C hlamydomonas reinhardtii using a type‐2 diacylglycerol acyltransferase with a phosphorus starvation–inducible promoter
Author(s) -
Iwai Masako,
Ikeda Keiko,
Shimojima Mie,
Ohta Hiroyuki
Publication year - 2014
Publication title -
plant biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.525
H-Index - 115
eISSN - 1467-7652
pISSN - 1467-7644
DOI - 10.1111/pbi.12210
Subject(s) - chlamydomonas reinhardtii , biology , thylakoid , biochemistry , cytosol , acyltransferase , chloroplast , enzyme , gene , mutant
Summary When cultivated under stress conditions, many plants and algae accumulate oil. The unicellular green microalga C hlamydomonas reinhardtii accumulates neutral lipids (triacylglycerols; TAG s) during nutrient stress conditions. Temporal changes in TAG levels in nitrogen (N)‐ and phosphorus (P)‐starved cells were examined to compare the effects of nutrient depletion on TAG accumulation in C. reinhardtii . TAG accumulation and fatty acid composition were substantially changed depending on the cultivation stage before nutrient starvation. Profiles of TAG accumulation also differed between N and P starvation. Logarithmic‐growth‐phase cells diluted into fresh medium showed substantial TAG accumulation with both N and P deprivation. N deprivation induced formation of oil droplets concomitant with the breakdown of thylakoid membranes. In contrast, P deprivation substantially induced accumulation of oil droplets in the cytosol and maintaining thylakoid membranes. As a consequence, P limitation accumulated more TAG both per cell and per culture medium under these conditions. To enhance oil accumulation under P deprivation, we constructed a P deprivation‐dependent overexpressor of a C hlamydomonas type‐2 diacylglycerol acyl‐CoA acyltransferase ( DGTT 4) using a sulphoquinovosyldiacylglycerol 2 ( SQD 2 ) promoter, which was up‐regulated during P starvation. The transformant strongly enhanced TAG accumulation with a slight increase in 18 : 1 content, which is a preferred substrate of DGTT 4. These results demonstrated enhanced TAG accumulation using a P starvation–inducible promoter.