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M Hamberg

Publications and source records attributed to M Hamberg.

At least 37 records · Page 2Linked to original sources
PubMed1998

A pathway for biosynthesis of divinyl ether fatty acids in green leaves.

[1-14C]alpha-Linolenic acid was incubated with a particulate fraction of homogenate of leaves of the meadow buttercup (Ranunculus acris L.). The main product was a divinyl ether fatty acid, which was identified as 12-[1'(Z),3'(Z)-hexadienyloxy]-9(Z),11(E)-dodecadienoic acid. Addition of glutathione peroxidase and reduced glutathione to incubations of alpha-linolenic acid almost completely suppressed formation of the divinyl ether acid and resulted in the appearance of 13(S)-hydroxy-9(Z), 11(E),15(Z)-octadecatrienoic acid as the main product. This result, together with the finding that 13(S)-hydroperoxy-9(Z), 11(E),15(Z)-octadecatrienoic acid served as an efficient precursor of the divinyl ether fatty acid, indicated that divinyl ether biosynthesis in leaves of R. acris occurred by a two-step pathway involving an omega6-lipoxygenase and a divinyl ether synthase. Incubations of isomeric hydroperoxides derived from alpha-linolenic and linoleic acids with the enzyme preparation from R. acris showed that 13(S)-hydroperoxy-9(Z),11(E)-octadecadienoic acid was transformed into the divinyl ether 12-[1'(Z)-hexenyloxy]-9(Z), 11(E)-dodecadienoic acid. In contrast, neither the 9(S)-hydroperoxides of linoleic or alpha-linolenic acids nor the 13(R)-hydroperoxide of alpha-linolenic acid served as precursors of divinyl ethers.

Chlorophyll↗
PubMed1997

Mutation of tyrosine 383 in leukotriene A4 hydrolase allows conversion of leukotriene A4 into 5S,6S-dihydroxy-7,9-trans-11,14-cis-eicosatetraenoic acid. Implications for the epoxide hydrolase mechanism.

Leukotriene A4 hydrolase is a bifunctional zinc metalloenzyme that catalyzes the final step in the biosynthesis of the proinflammatory mediator leukotriene B4. In previous studies with site-directed mutagenesis on mouse leukotriene A4 hydrolase, we have identified Tyr-383 as a catalytic amino acid involved in the peptidase reaction. Further characterization of the mutants in position 383 revealed that [Y383H], [Y383F], and [Y383Q] leukotriene A4 hydrolases catalyzed hydrolysis of leukotriene A4 into a novel enzymatic metabolite. From analysis by high performance liquid chromatography, gas chromatography/mass spectrometry of material generated in the presence of H216O or H218O, steric analysis of the hydroxyl groups, treatment with soybean lipoxygenase, and comparison with a synthetic standard, the novel metabolite was assigned the structure 5S, 6S-dihydroxy-7,9-trans-11,14-cis-eicosatetraenoic acid (5S,6S-DHETE). The kinetic parameters for the formation of 5S,6S-DHETE and leukotriene B4 were found to be similar. Also, both activities were susceptible to suicide inactivation and were equally sensitive to inhibition by bestatin. Moreover, from the stereochemical configuration of the vicinal diol, it could be inferred that 5S, 6S-DHETE is formed via an SN1 mechanism involving a carbocation intermediate, which in turn indicates that enzymatic hydrolysis of leukotriene A4 into leukotriene B4 follows the same mechanism. Inasmuch as soluble epoxide hydrolase utilizes leukotriene A4 as substrate to produce 5S,6R-DHETE, our results also suggest a functional relationship between leukotriene A4 hydrolase and xenobiotic epoxide hydrolases.

Aminopeptidases↗
PubMed1997

Myoglobin-catalyzed bis-allylic hydroxylation and epoxidation of linoleic acid.

Linoleic acid was treated with metmyoglobin and cumene hydroperoxide at 0 degrees C under anaerobic conditions. Five major compounds were identified, i.e., 11-hydroxylinoleic acid (29% yield), cis-9,10-epoxy-(12Z)-octadecenoic acid (16%), cis-12,13-epoxy-(9Z)-octadecenoic acid (8%), 9-hydroxy-(10E,12Z)-octadecadienoic acid (4%), and 13-hydroxy-(9Z,11E)-octadecadienoic acid (4%). Steric analysis showed that these compounds were all racemic. The steric course of the formation of the major metabolite, (11R,S)-hydroxylinoleic acid, was studied by incubation of linoleic acids stereospecifically deuterated at C-11. It was found that the (11R)-hydroxylinoleic acid lost most of the deuterium label when formed from [(11R)-2H]linoleic acid but retained the label when formed from [(11S)-2H]linoleic acid. Furthermore, the (11S)-hydroxylinoleic acid retained and lost most of the label when produced from [(11R)-2H]- and [(11S)-2H]linoleic acids, respectively. Thus, although the myoglobin-promoted hydroxylation of linoleic acid into 11-hydroxylinoleic acid lacked apparent stereospecificity and produced equal amounts of the R and S enantiomers, the course of the reaction was stereospecific and involved hydrogen abstraction and oxygen insertion occurring with retention of absolute configuration of the carbon atom hydroxylated.

Benzene Derivatives↗
PubMed1997

On the mechanism of biosynthesis of divinyl ether oxylipins by enzyme from garlic bulbs.

The microsomal fraction of homogenate of garlic (Allium sativum L.) bulbs contains a divinyl ether synthase which catalyzes conversion of (9Z,11E,13S)-13-hydroperoxy-9, 11-octadecadienoic acid and (9Z,11E,13S,15Z)-13-hydroperoxy-9,11,15-octadecatri eno ic acid into (9Z,11E,1'E,)-12-(1'-hexenyloxy)-9,11-dodecadienoic acid (etherolenic acid) and (9Z,11E,1'E,3'Z)-12-(1',3'-hexadienyloxy)-9,11-dode cadienoic acid (etherolenic acid), respectively. Two isomers of etherolenic acid were isolated. As shown by NMR spectrometry, the double bond configurations of these compounds were (9E,11E,1'E) and (9Z,11Z,1'E). Experiments with linoleic acid (13R,S)-hydroperoxide demonstrated that the S enantiomer was a much better substrate for the divinyl ether synthase compared to the R enantiomer. Incubation of (9Z,11E,13S)-[18O2]hydroperoxy-9,11-octadecadienoic acid led to the formation of etherolenic acid which retained 18O in the ether oxygen. An intermediary role of an epoxyallylic cation in etherolenic acid biosynthesis is postulated.

Chromatography, High Pressure Liquid↗
PubMed1996

Divinyl ether synthase from garlic (Allium sativum L.) bulbs: sub-cellular localization and substrate regio-and stereospecificity.

Sub-cellular localization and some properties of 13-hydroperoxide-specific divinyl ether synthase from garlic bulbs were studied. Sub-cellular fractions from garlic bulbs were incubated with [1-(14)C](9Z,11E,13S)-13-hydroperoxy-9,11-octadecadienoic acid (13-HPOD). The predominant part of divinyl ether synthase activity from garlic bulbs was found in the microsomal fraction. The enzyme utilizes 13(S)-HPOD as its preferential substrate. Other hydroperoxides, including 9(S)-HPOD, gave much poorer yields of divinyl ethers. Unreacted hydroperoxide after incubation of 13(R,S)-HPOD with enzyme was composed of up to 94% 13(R)-HPOD. Thus, divinyl ether synthase possesses stereoselectivity, utilizing preferentially the (S)-enantiomer.

Cytochrome P-450 Enzyme System↗
PubMed1996

Formation of a novel enzymatic metabolite of leukotriene A4 in tissues of Xenopus laevis.

Leukotriene-A4, hydrolase catalyzes the final step in the biosynthesis of the potent proinflammatory mediator leukotriene B4. Previously, leukotriene-A4 hydrolase has been characterized from human, mouse and rat sources, i.e. only from mammalian species. In the present investigation, expression of leukotriene-A4, hydrolase was studied in organs of Xenopus laevis. Enzyme activity was found in all nine organs tested with the highest levels in the intestine and the reproductive organs, i.e. oocytes and testes, previously unrecognized rich sources of the enzyme. No immunoreactive leukotriene-A4 hydrolase was detected in Western blots of 10000Xg supernatants of X. laevis organ homogenates, using a polyclonal antiserum raised against human leukotriene-A4 hydrolase. Likewise, Northern blot analysis of liver total RNA did not detect Xenopus leukotriene-A4 hydrolase mRNA using a human CDNA probe. These results indicate significant structural differences between the human and toad enzymes. Incubations of 10000Xg supernatants of organ homogenates with leukotriene A4 revealed the formation of a novel metabolite, denoted compound X. Conversion of leukotriene A4 into compound X was due to an enzymatic activity as judged by its protein dependence, heat sensitivity, and resistance to ultrafiltration, and this activity appeared to be linked, directly or indirectly,, to leukotriene A4 hydrolase. From data obtained by ultraviolet spectrophotometry, gas chromatography coupled to mass spectrometry, ultraviolet-induced isomerization, and comparison with a synthetic standard, compound X was assigned the structure 5S,12R-dihydroxy-6,10-trans-8,14-cis-eicosatetraenoic acid. Finally, compound X was found to exhibit contractile activity in guinea-pig lung parenchyma, apparently elicited via a leukotriene B receptor.

Animals↗
PubMed1996

Mechanism of linoleic acid hydroperoxide reaction with alkali.

Treatment of (13S,9Z,11E)-13-hydroperoxy-9,11-octadecadienoic acid (13S-HPODE) with strong alkali resulted in the formation of about 75% of the corresponding hydroxy acid, (13S,9Z,11E)-13-hydroxy-9,11-octadecadienoic acid (13S-HODE), and the remaining 25% of products was a mixture of several oxidized fatty acids, the majority of which was formed from (9Z,11R,S,12S,R)-13-oxo-11,12-epoxy-9-octadecenoic acid by Favorskii rearrangement (Gardner, H.W., et al. (1993) Lipids 28, 487-495). In the present work, isotope experiments were completed in order to get further information about the initial steps of the alkali-promoted decomposition of 13S-HPODE. 1. Reaction of [hydroperoxy-18O2] 13S-HPODE with 5 M KOH resulted in the formation of [hydroxy-18O] 13S-HODE and [epoxy-18O](9Z,11R,S,12S,R)-13-oxo-11,12-epoxy-9-octadecenoi c acid; 2. treatment of a mixture of [U-14C] 13S-HODE and [hydroperoxy-18O2] 13S-HPODE with KOH and analysis of the reaction product by radio-TLC showed that 13S-HODE was stable under the reaction conditions and did not serve as precursor of other products; 3. reaction of a mixture of [U-14C] 13-oxo-9,11-octadecadienoic acid (13-OODE) and [hydroperoxy-18O2] 13S-HPODE with KOH resulted in the formation of [U-14C-epoxy-18O]99Z,11R,S,12S,R)-13-oxo-11,12-epoxy-9-octad ecenoic acid; 4. treatment of a mixture of [hydroperoxy-18O2] 13S-HPODE and [carboxyl-18O1] 13S-HPODE with KOH afforded (9Z,11R,S,12S,R)-13-oxo-11,12-epoxy-9-octadecenoic acid having an 18O-labeling pattern which was in agreement with its formation by intermolecular epoxidation. It was concluded that (9Z,11R,S,12S,R)-13-oxo-11,12-epoxy-9-octadecenoic acid is formed from 13S-HPODE by a sequence involving initial dehydration into the alpha, beta-unsaturated ketone, 13-OODE, followed by epoxidation of the delta 11 double bond of this compound by the peroxyl anion of a second molecule of 13S-HPODE. Rapid conversion of hydroperoxides by alkali appeared to require the presence of an alpha, beta-unsaturated ketone intermediate as an oxygen acceptor. This was supported by experiments with a saturated hydroperoxide, methyl 12-hydroperoxyoctadecanoate, which was found to be much more resistant to alkali-promoted conversion than 13S-HPODE.

Alkalies↗
PubMed1996

Specificity of two lipoxygenases from rice: unusual regiospecificity of a lipoxygenase isoenzyme.

The regio- and stereospecificity of two lipoxygenases from rice were investigated using arachidonic acid as the substrate. Rice seed lipoxygenase-2 (RSL-2) catalyzed oxygenation of arachidonic acid into a mixture of 5(S)-hydroperoxy-6,8,11,14-eicosatetraenoic acid [5(S)-HPETE] and 15(S)-hydroperoxy-5,8,11,13-eicosatetraenoic acid [15(S)-HPETE]. In addition, two double dioxygenase products, 5(S), 15(S)-dihydroperoxy-6,8,11,13 -eicosatetraenoic acid and 8(S),15(S)-dihydroperoxy-5,9,11,13 -eicosatetraenoic acid, were obtained in a lower yield. The regiospecificity of the RSL-2-catalyzed oxygenation was pH-dependent. Thus, incubation at pH 6.7 led to the formation of 5(S)-HPETE and 15(S)-HPETE in a ratio of 52:48, and incubation at pH 9.8 strongly suppressed production of 5(S)-HPETE and led to formation of 5(S)-HPETE and 15(S)-HPETE in a ratio of 3:97. A pH-dependent orientation of arachidonic acid at the active site is proposed to explain these findings. Rice leaf pathogen-inducible lipoxygenase [Peng, Y.-L., Shirano, Y., Ohta, H., Hibino, T., Tanaka, K., and Shibata, D. (1994) J. Biol. Chem. 269, 3755-3761] catalyzed oxygenation of arachidonic acid into a single hydroperoxide isomer of high optical purity, i.e., 15(S)-HPETE (99.5% S).

Arachidonic Acid↗
PubMed1996

Stereochemical aspects of fatty acid oxidation: hydroperoxide isomerases.

Lipoxygenases catalyze dioxygenation of polyunsaturated fatty acids to produce fatty-acid hydroperoxides. The reaction involves initial stereospecific abstraction of a hydrogen atom from a bis-allylic methylene group followed by antarafacial attack by dioxygen at one of the terminal carbon atoms of the pentadienyl radical. 8(R)-Dioxygenase, recently discovered in the fungus Gaeumannomyces graminis, catalyzes formation of 8-hydroperoxy derivatives of linoleic and oleic acids by abstracting one hydrogen from C-8 and inserting dioxygen at the same carbon atom. Isotope-labeling studies show that the configuration at C-8 is inverted during this process. The fungus Saprolegnia parasitica, a fish parasite, contains an omega 6-lipoxygenase and an epoxy alcohol synthase. The latter enzyme catalyzes isomerization of fatty acid hydroperoxides into alpha,beta- and gamma,delta-epoxy alcohols. Experiments with 18O-labelled hydroperoxides demonstrate that the hydroperoxide --> epoxy alcohol conversion consists of intramolecular transfer of the terminal hydroperoxide oxygen to either of the two conjugated double bonds. The reactions proceed with retention of geometrical configuration, i.e. epoxidation of the alpha,beta (E) and gamma,delta (Z) double bonds of the parent fatty acid hydroperoxide gives rise to trans and cis epoxides, respectively. G. graminis, as well as the marine red alga Gracilariopsis lemaneiformis, contain vicinal diol synthases that catalyze isomerization of fatty-acid hydroperoxides into vicinal dihydroxy fatty acids. Studies using 18O-labelled hydroperoxides show that the hydroperoxide --> diol conversions occur by intramolecular transfer of the terminal hydroperoxide oxygen to the vicinal methylene group. Experiments with stereospecifically deuteriated fatty-acid hydroperoxides demonstrate that the intramolecular hydroxylations catalyzed by the two vicinal diol synthases proceed with retention of absolute configuration of the carbon hydroxylated.

Animals↗
PubMed1995

Quantitative determination of 8-hydroxyguanine and guanine by isotope dilution mass spectrometry.

8-[4,5,6,8-13C4]Hydroxyguanine and [4,5,6-13C3]guanine were prepared by total synthesis. The labeled compounds were used as internal standards in a gas-liquid chromatographic-mass spectrometric method for quantitative determination of 8-hydroxyguanine and guanine in DNA. The approach used made it possible to directly determine the ratio between 8-hydroxyguanine and guanine, expressed as the number of molecules of 8-hydroxyguanine per 10(5) molecules of guanine, in the sample of DNA analyzed. A method for trimethylsilylation of 8-hydroxyguanine and guanine at room temperature was developed. Use of this method for derivatization gave levels of 8-hydroxyguanine in calf thymus DNA which were lower than those recently found by gas chromatography-mass spectrometry but similar to those determined by high-performance liquid chromatography with electrochemical detection.

Animals↗
PubMed1995

Arachidonic acid metabolism in the human mast cell line HMC-1: 5-lipoxygenase gene expression and biosynthesis of thromboxane.

Metabolism of arachidonic acid was studied in the unique human mast cell line HMC-1. By HPLC and/or gas chromatography mass spectrometry (GC-MS), 19 oxygenated metabolites were identified, including monohydroxy acids, leukotrienes, prostaglandins, and thromboxane. Intact cells incubated with the calcium ionophore A23187 and arachidonic acid expressed 5-lipoxygenase activity and produced 5-hydroxyeicosatetraenoic acid (5-HETE) as the major metabolite (745 pmol/10(7) cells) followed by leukotriene (LT) C4 (245 pmol/10(7) cells) and 11-trans-LTC4 (74 pmol/10(7) cells). Low but clearly detectable levels of LTB4 were also observed. The total amounts of 5-LO products were comparable to those obtained with RBL-1 cells and corresponded to approx. 30% of the levels obtained with isolated human polymorphonuclear leukocytes. Time-course experiments revealed that HMC-1 cells contained the enzyme activities required to metabolize LTC4 into LTD4 and further into LTE4. The profile of prostanoids included, prostaglandin (PG) E2, PGF2 alpha, and PGD2, whereas 6-keto-PGF1 alpha, reflecting prostacyclin formation, could not be detected. Furthermore, we were able to unambiguously establish that HMC-1 cells could produce substantial amounts of thromboxane (TX) A2, measured as TXB2 (0.1-2.2 nmol/10(7) cells). Generation of TXA2 in such quantities, exceeding those of LTC4, suggests that mast cells may be an important source of thromboxane and points to a possible role for these cells in hemostasis and thrombosis. After approx. 10 passages in culture, 5-lipoxygenase activity in HMC-1 cells drastically declined concomitantly with changes in growth behavior and cell morphology. Analysis by Northern and Western blots revealed that loss of 5-lipoxygenase activity correlated well with a reduced 5-lipoxygenase gene expression at both a transcriptional and translational level. This loss of enzyme activity and gene expression may be related to a genetic abnormality propagated in HMC-1 cells, i.e., a 10;16 translocation, which thus involves the chromosome containing the 5-lipoxygenase gene.

Arachidonate 5-Lipoxygenase↗
PubMed1995

Growth hormone signaling leading to CYP2C12 gene expression in rat hepatocytes involves phospholipase A2.

The expression of CYP2C12 is liver-specific and regulated at the transcriptional level by growth hormone (GH). In attempts to elucidate the nature of signaling molecules mediating the GH regulation of this gene in rat hepatocytes, a role for phospholipase A2 (PLA2) as a transducer of GH-induced levels of P4502C12 mRNA was investigated. GH was shown to induce tyrosyl-phosphorylation of p42 and p44 microtubule-associated protein (MAP) kinases and to reduce the electrophoretic mobility of a 100-kDa protein, immunologically related to cPLA2. These events were observed in parallel with GH-stimulated release of [3H]arachidonic acid ([3H]AA) from cellular phospholipids of rat hepatocytes labeled with [3H]AA. These rapid effects of GH action, as well as the GH-induced expression of CYP2C12, were inhibited in cells treated with the tyrosine kinase inhibitor herbimycin A. Similarly, when the GH-induced liberation of [3H]AA was blocked by the PLA2 inhibitor mepacrine or the Ca2+ channel blocker verapamil, GH-induced accumulation of P4502C12 mRNA was absent. These results suggest a correlation between PLA2 activity and GH regulation of the CYP2C12 gene. The inhibitory effect of mepacrine on GH induction of P4502C12 mRNA was reversed by AA addition, further supporting a role for eicosanoids in the regulation of CYP2C12. Finally, inhibitors of P450-mediated AA metabolism, SKF-525A and ketoconazole as well as eicosatetraynoic acid, blocked the GH-mediated induction of P4502C12 mRNA, whereas more specific inhibitors of cyclooxygenase or lipoxygenase metabolism did not. Based on these results, we suggest that GH signaling in rat hepatocytes, leading to increased expression of CYP2C12, involves PLA2 activation and subsequent P450-catalyzed formation of an active AA metabolite.

5,8,11,14-Eicosatetraynoic Acid↗
PubMed1995

Human thioredoxin reductase directly reduces lipid hydroperoxides by NADPH and selenocystine strongly stimulates the reaction via catalytically generated selenols.

Human placenta thioredoxin reductase (HP-TR) in the presence of NADPH-catalyzed reduction of (15S)-hydroperoxy-(5Z),(8Z),11(Z),13(E)-eicosatetraenoic acid ((15S)-HPETE) into the corresponding alcohol ((15S)-HETE). Incubation of 50 nM HP-TR and 0.5 mM NADPH with 300 microM 15-HPETE for 5 min resulted in formation of 16.5 microM 15-HETE. After 60 min, 74.7 microM 15-HPETE was reduced. The rate of the reduction of 15-HPETE by the HP-TR/NADPH peroxidase system was increased 8-fold by the presence of 2.5 microM selenocystine, a diselenide amino acid. In this case, 15-HPETE was catalytically reduced by the selenol amino acid, selenocysteine, generated from the diselenide by the HP-TR/NADPH system. To a smaller extent, selenodiglutathione or human thioredoxin also potentiated the reduction of 15-HPETE by HP-TR. Hydrogen peroxide and 15-HPETE were reduced at approximately the same rate by HP-TR, thioredoxin, and selenocystine. In contrast, t-butyl hydroperoxide was reduced at a 10-fold lower rate. Our data suggest two novel pathways for the reduction and detoxification of lipid hydroperoxides, hydrogen peroxide, and organic hydroperoxides, i.e. the human thioredoxin reductase-dependent pathway and a coupled reduction in the presence of selenols or selenide resulting from the reduction of selenocystine or selenodiglutathione.

Catalysis↗