Effects of methyl sterculate on acyl lipid metabolism in Rhodotorula gracilis (CBS 3043)

1987 ◽  
Vol 15 (4) ◽  
pp. 632-633
Author(s):  
C. E. ROLPH ◽  
R. S. MORETON ◽  
J. L. HARWOOD
1986 ◽  
Vol 14 (4) ◽  
pp. 712-712 ◽  
Author(s):  
C. E. ROLPH ◽  
R. S. MORETON ◽  
I. S. SMALL ◽  
J. L. HARWOOD

BMC Genomics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 271 ◽  
Author(s):  
Juan Yu ◽  
Zhenhai Zhang ◽  
Jiangang Wei ◽  
Yi Ling ◽  
Wenying Xu ◽  
...  

Cells ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 2326
Author(s):  
Sylwia Klińska ◽  
Sara Kędzierska ◽  
Katarzyna Jasieniecka-Gazarkiewicz ◽  
Antoni Banaś

Acyl-lipids are vital components for all life functions of plants. They are widely studied using often in vitro conditions to determine inter alia the impact of genetic modifications and the description of biochemical and physiological functions of enzymes responsible for acyl-lipid metabolism. What is currently lacking is knowledge of if these results also hold in real environments—in in vivo conditions. Our study focused on the comparative analysis of both in vitro and in vivo growth conditions and their impact on the acyl-lipid metabolism of Camelina sativa leaves. The results indicate that in vitro conditions significantly decreased the lipid contents and influenced their composition. In in vitro conditions, galactolipid and trienoic acid (16:3 and 18:3) contents significantly declined, indicating the impairment of the prokaryotic pathway. Discrepancies also exist in the case of acyl-CoA:lysophospholipid acyltransferases (LPLATs). Their activity increased about 2–7 times in in vitro conditions compared to in vivo. In vitro conditions also substantially changed LPLATs’ preferences towards acyl-CoA. Additionally, the acyl editing process was three times more efficient in in vitro leaves. The provided evidence suggests that the results of acyl-lipid research from in vitro conditions may not completely reflect and be directly applicable in real growth environments.


2003 ◽  
Vol 132 (2) ◽  
pp. 681-697 ◽  
Author(s):  
Frédéric Beisson ◽  
Abraham J.K. Koo ◽  
Sari Ruuska ◽  
Jörg Schwender ◽  
Mike Pollard ◽  
...  

Author(s):  
Yixin Cui ◽  
Xiao Zeng ◽  
Qing Xiong ◽  
Dayong Wei ◽  
Jinghang Liao ◽  
...  

Abstract In crops there are quantitative trait loci (QTLs) in which some of the causal quantitative trait genes (QTGs) have not been functionally characterized even in the model plant Arabidopsis. We propose an approach to delineate QTGs in rapeseed by coordinating expression of genes located within QTLs and known orthologs related to traits from Arabidopsis. Using this method in developing siliques 15 d after pollination in 71 lines of rapeseed, we established an acyl-lipid metabolism co-expression network with 21 modules composed of 270 known acyl-lipid genes and 3503 new genes. The core module harbored 76 known genes involved in fatty acid and triacylglycerol biosynthesis and 671 new genes involved in sucrose transport, carbon metabolism, amino acid metabolism, seed storage protein processes, seed maturation, and phytohormone metabolism. Moreover, the core module closely associated with the modules of photosynthesis and carbon metabolism. From the co-expression network, we selected 12 hub genes to identify their putative Arabidopsis orthologs. These putative orthologs were functionally analysed using Arabidopsis knockout and overexpression lines. Four knockout mutants exhibited lower seed oil content, while the seed oil content in 10 overexpression lines was significantly increased. Therefore, combining gene co-expression network analysis and QTL mapping, this study provides new insights into the detection of QTGs and into acyl-lipid metabolism in rapeseed.


2013 ◽  
Vol 11 ◽  
pp. e0161 ◽  
Author(s):  
Yonghua Li-Beisson ◽  
Basil Shorrosh ◽  
Fred Beisson ◽  
Mats X. Andersson ◽  
Vincent Arondel ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document