Effect of Cholesterol on Macromolecular Synthesis and Fatty Acid Uptake by Mycoplasma Capricolum
Overview
Affiliations
The rates of protein and lipid synthesis of Mycoplasma capricolum were essentially synchronous during growth and depended on the sterol supplement in the media increasing in the order cholesterol (0.5 microgram/ml) < lanosterol (10 microgram/ml) < lanosterol (10 microgram/ml) + cholesterol (0.5 microgram/ml) < cholesterol (10 microgram/ml). The effect of lanosterol plus low cholesterol on macromolecular synthesis was synergistic. Whereas protein and lipid synthesis were brought virtually to a halt by cholesterol starvation, DNA synthesis continued for about 8 h. Increasing the palmitate and elaidate concentrations 4-fold in the lanosterol-supplemented media raised the growth rate even in the absence of the small amount of cholesterol (0.5 microgram/ml) needed otherwise for the synergistic effect on growth. Studies of the kinetics of fatty acid uptake by resting cells showed that the apparent Km (17 microM) of oleate uptake in lanosterol-grown cells was specifically lowered to 3 microM, a value equal to that seen in cholesterol-grown cells, by the inclusion of a synergistic amount of cholesterol in the growth media. By contrast, the apparent Km for palmitate uptake was the same (2 microM) for all three cell types. The results are consistent with the membrane cholesterol serving in a dual role, one as a bulk component and another more specific function involving the regulation of unsaturated fatty acid uptake and thereby phospholipid biosynthesis.
Model-driven design allows growth of Mycoplasma pneumoniae on serum-free media.
Gaspari E, Malachowski A, Garcia-Morales L, Burgos R, Serrano L, Martins Dos Santos V NPJ Syst Biol Appl. 2020; 6(1):33.
PMID: 33097709 PMC: 7584665. DOI: 10.1038/s41540-020-00153-7.
Mesoscale Assembly of Bisteroidal Esters from Terephthalic Acid.
Guerrero-Luna G, Hernandez-Linares M, Bernes S, Carrasco-Carballo A, Montalvo-Guerrero D, Fernandez-Herrera M Molecules. 2020; 25(5).
PMID: 32182644 PMC: 7179421. DOI: 10.3390/molecules25051213.
Rodriguez R, Arunachalam T, Parks L, Caspi E Lipids. 2016; 18(11):772-5.
PMID: 27519987 DOI: 10.1007/BF02534634.
Using Sterol Substitution to Probe the Role of Membrane Domains in Membrane Functions.
Kim J, London E Lipids. 2015; 50(8):721-34.
PMID: 25804641 PMC: 5021220. DOI: 10.1007/s11745-015-4007-y.
Rodriguez-Acebes S, de la Cueva P, Fernandez-Hernando C, Ferruelo A, Lasuncion M, Rawson R Biochem J. 2009; 420(2):305-15.
PMID: 19260826 PMC: 2931812. DOI: 10.1042/BJ20081909.