scholarly journals The Saccharomyces cerevisiae EHT1 and EEB1 Genes Encode Novel Enzymes with Medium-chain Fatty Acid Ethyl Ester Synthesis and Hydrolysis Capacity

2006 ◽  
Vol 281 (7) ◽  
pp. 4446-4456 ◽  
Author(s):  
Sofie M.G. Saerens ◽  
Kevin J. Verstrepen ◽  
Stijn D.M. Van Laere ◽  
Arnout R.D. Voet ◽  
Patrick Van Dijck ◽  
...  
2019 ◽  
Vol 16 (14) ◽  
pp. 1304-1316
Author(s):  
Nhan Thi Thuc Truong ◽  
Arnupong Suttichaiya ◽  
Wikanda Hiamhoen ◽  
Peerapat Thinnongwaeng ◽  
Chaloemkwan Ariyawong ◽  
...  

2000 ◽  
Vol 150 (3) ◽  
pp. 489-498 ◽  
Author(s):  
Carlo W.T. van Roermund ◽  
Henk F. Tabak ◽  
Marlene van den Berg ◽  
Ronald J.A. Wanders ◽  
Ewald H. Hettema

The Saccharomyces cerevisiae peroxisomal membrane protein Pex11p has previously been implicated in peroxisome proliferation based on morphological observations of PEX11 mutant cells. Pex11p-deficient cells fail to increase peroxisome number in response to growth on fatty acids and instead accumulate a few giant peroxisomes. We report that mutants deficient in genes required for medium-chain fatty acid (MCFA) β-oxidation display the same phenotype as Pex11p-deficient cells. Upon closer inspection, we found that Pex11p is required for MCFA β-oxidation. Disruption of the PEX11 gene results in impaired formation of MCFA-CoA esters as measured in intact cells, whereas their formation is normal in cell lysates. The sole S. cerevisiae MCFA-CoA synthetase (Faa2p) remains properly localized to the inner leaflet of the peroxisomal membrane in PEX11 mutant cells. Therefore, the in vivo latency of MCFA activation observed in Pex11p-deficient cells suggests that Pex11p provides Faa2p with substrate. When PEX11 mutant cells are shifted from glucose to oleate-containing medium, we observed an immediate deficiency in β-oxidation of MCFAs whereas giant peroxisomes and a failure to increase peroxisome abundance only became apparent much later. Our observations suggest that the MCFA oxidation pathway regulates the level of a signaling molecule that modulates the number of peroxisomal structures in a cell.


Author(s):  
Tony Treloar ◽  
Lesley J. Madden ◽  
Joel S. Winter ◽  
Jeffrey L. Smith ◽  
John de Jersey

Alcohol ◽  
1999 ◽  
Vol 17 (3) ◽  
pp. 241-245 ◽  
Author(s):  
Kendrick A Goss ◽  
Rami Alharethi ◽  
Michael Laposata

2021 ◽  
Vol 21 (2) ◽  
Author(s):  
Leonie Baumann ◽  
Tyler Doughty ◽  
Verena Siewers ◽  
Jens Nielsen ◽  
Eckhard Boles ◽  
...  

ABSTRACT The medium-chain fatty acid octanoic acid is an important platform compound widely used in industry. The microbial production from sugars in Saccharomyces cerevisiae is a promising alternative to current non-sustainable production methods, however, titers need to be further increased. To achieve this, it is essential to have in-depth knowledge about the cell physiology during octanoic acid production. To this end, we collected the first RNA-Seq data of an octanoic acid producer strain at three time points during fermentation. The strain produced higher levels of octanoic acid and increased levels of fatty acids of other chain lengths (C6–C18) but showed decreased growth compared to the reference. Furthermore, we show that the here analyzed transcriptomic response to internally produced octanoic acid is notably distinct from a wild type's response to externally supplied octanoic acid as reported in previous publications. By comparing the transcriptomic response of different sampling times, we identified several genes that we subsequently overexpressed and knocked out, respectively. Hereby we identified RPL40B, to date unknown to play a role in fatty acid biosynthesis or medium-chain fatty acid tolerance. Overexpression of RPL40B led to an increase in octanoic acid titers by 40%.


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