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16899-03-9

5-Hydroxytetradecansaeure synthesis

2synthesis methods
544-63-8 Synthesis
Myristic acid

544-63-8
625 suppliers
$5.00/5g

5-Hydroxytetradecansaeure

16899-03-9
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17278-73-8 Synthesis
13-Hydroxymyristic acid

17278-73-8
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Yield:-

Reaction Conditions:

with 2,3,4,5,6-pentahydroxy-hexanal;cytochrome b5;glucose dehydrogenase from Bacillus megaterium;rabbit cytochrome P450 monooxygenase;rat cytochrome P450 reductase;1,2-dilauroyl-sn-glicero-3-phosphatidylcholine;NADPH;superoxide dismutase;catalase from bovine liver in aq. phosphate buffer;dimethyl sulfoxide at 30; pH=7.5;Enzymatic reaction;

Steps:

2.4 Fatty acid and fatty alcohol conversion by CYP4B1

General procedure: Conversions of fatty acids 1-8 and fatty alcohols 9-12 were carried out in 50mM potassium phosphate buffer, pH 7.5 and a total reaction volume of 100μL. Reaction mixtures contained 0.25μM CYP4B1, 0.5μM CPR, 0.25μM cytochrome b5, 100 U mL-1 superoxide dismutase, 1000 UmL-1 catalase, 25 U mL-1 GDH, 20mM glucose, 25μgmL-1 DLPC, 200μM substrate (from a 10mM stock solution dissolved in DMSO) and 200μM NADPH. Samples were incubated at 30°C for 90min; this reaction time was chosen as an almost complete substrate conversion (as achieved for C12 4 after 120min) was not desirable, so as to allow comparison of the conversion values for the individual substrates and also between the two CYP4B1 isoforms.

References:

Thesseling, Florian A.;Hutter, Michael C.;Wiek, Constanze;Kowalski, John P.;Rettie, Allan E.;Girhard, Marco [Archives of Biochemistry and Biophysics,2020,vol. 679,art. no. 108216]