Literature DB >> 3343228

Microsomal preparation from an animal tissue catalyzes release of carbon monoxide from a fatty aldehyde to generate an alkane.

T M Cheesbrough1, P E Kolattukudy.   

Abstract

Alkanes are widely distributed in nature and impaired alkane synthesis was implicated in certain neurological disorders. However, the mechanism of synthesis of alkanes in animals is unknown. Our search to find a convenient animal tissue to study alkane biosynthesis resulted in the finding that the uropygial gland (a modified sebaceous gland) of the eared grebe (Podiceps nigricollis) produces large amounts of alkanes. These alkanes, which constitute 35-41% of the total lipid produced, are mainly C21, C23, C25, and C27 n-alkanes. Cell free homogenates of this tissue synthesized alkanes from both fatty acid and aldehyde in the absence of O2. Differential centrifugation of the homogenates indicated that this activity was located in the microsomal fraction. With isolated microsomes conversion of fatty acid to alkane required CoA, ATP, and NADH whereas conversion of an aldehyde to alkane did not require the addition of cofactors. That the final step in alkane synthesis is a decarbonylation was shown by the stoichiometric production of heptadecane and CO from octadecanal. CO was identified by adsorption to RhCl [(C6H6)3P]3 and oxidation of the trapped CO to CO2 by watergas shift reaction. The enzyme preparation also catalyzed incorporation of 14C from 14CO into octadecanal showing the reversible nature of the decarbonylase. This decarbonylase had a sharp pH optimum at 7.0, a Kapp of 180 microM and a V1/2 of 90 rho mol/min/mg protein for octadecanal. The enzyme was inhibited by the metal chelators EDTA, O-phenanthroline, and 8-hydroxyquinoline, but not by KCN. It was stimulated nearly 3-fold by 5 microM 2-mercaptoethanol and inhibited by the presence of O2. During the conversion of [1-3H]octadecanal to heptadecane, 3H was lost to water and 3H from 3H2O was incorporated into the alkane generated from unlabeled octadecanal. The mechanism of the decarbonylation and the nature of the enzyme remain to be elucidated.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3343228

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  17 in total

1.  Oxygen-independent alkane formation by non-heme iron-dependent cyanobacterial aldehyde decarbonylase: investigation of kinetics and requirement for an external electron donor.

Authors:  Bekir E Eser; Debasis Das; Jaehong Han; Patrik R Jones; E Neil G Marsh
Journal:  Biochemistry       Date:  2011-11-15       Impact factor: 3.162

Review 2.  Cyanobacterial alkane biosynthesis further expands the catalytic repertoire of the ferritin-like 'di-iron-carboxylate' proteins.

Authors:  Carsten Krebs; J Martin Bollinger; Squire J Booker
Journal:  Curr Opin Chem Biol       Date:  2011-04       Impact factor: 8.822

3.  Detection of formate, rather than carbon monoxide, as the stoichiometric coproduct in conversion of fatty aldehydes to alkanes by a cyanobacterial aldehyde decarbonylase.

Authors:  Douglas M Warui; Ning Li; Hanne Nørgaard; Carsten Krebs; J Martin Bollinger; Squire J Booker
Journal:  J Am Chem Soc       Date:  2011-02-22       Impact factor: 15.419

Review 4.  Divergent mechanisms of iron-containing enzymes for hydrocarbon biosynthesis.

Authors:  Courtney E Wise; Job L Grant; Jose A Amaya; Steven C Ratigan; Chun H Hsieh; Olivia M Manley; Thomas M Makris
Journal:  J Biol Inorg Chem       Date:  2016-12-21       Impact factor: 3.358

5.  Mechanistic insights from reaction of α-oxiranyl-aldehydes with cyanobacterial aldehyde deformylating oxygenase.

Authors:  Debasis Das; Benjamin Ellington; Bishwajit Paul; E Neil G Marsh
Journal:  ACS Chem Biol       Date:  2013-12-13       Impact factor: 5.100

6.  Aldehyde Decarbonylases: Enigmatic Enzymes of Hydrocarbon Biosynthesis.

Authors:  E Neil G Marsh; Matthew W Waugh
Journal:  ACS Catal       Date:  2013-11-01       Impact factor: 13.084

7.  New pathway for long-chain n-alkane synthesis via 1-alcohol in Vibrio furnissii M1.

Authors:  Myong-Ok Park
Journal:  J Bacteriol       Date:  2005-02       Impact factor: 3.490

8.  Terminal olefin (1-alkene) biosynthesis by a novel p450 fatty acid decarboxylase from Jeotgalicoccus species.

Authors:  Mathew A Rude; Tarah S Baron; Shane Brubaker; Murtaza Alibhai; Stephen B Del Cardayre; Andreas Schirmer
Journal:  Appl Environ Microbiol       Date:  2011-01-07       Impact factor: 4.792

9.  Unusual mechanism of hydrocarbon formation in the housefly: cytochrome P450 converts aldehyde to the sex pheromone component (Z)-9-tricosene and CO2.

Authors:  J R Reed; D Vanderwel; S Choi; J G Pomonis; R C Reitz; G J Blomquist
Journal:  Proc Natl Acad Sci U S A       Date:  1994-10-11       Impact factor: 11.205

10.  Probing the mechanism of cyanobacterial aldehyde decarbonylase using a cyclopropyl aldehyde.

Authors:  Bishwajit Paul; Debasis Das; Benjamin Ellington; E Neil G Marsh
Journal:  J Am Chem Soc       Date:  2013-04-02       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.