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Mechanistic investigations of the A-cluster of acetyl-CoA synthaseBramlett, Matthew Richard 12 April 2006 (has links)
The A-cluster of acetyl-CoA synthase (ACS) catalyzes the formation of acetyl-
CoA from CO, coenzyme-A, and a methyl group donated by a corrinoid iron-sulfur
protein. Recent crystal structures have exhibited three different metals, Zn, Cu, and Ni,
in the proximal site, which bridges a square-planar nickel site and a [Fe4S4] cubane.
Contradicting reports supported both the nickel and copper containing forms as
representing active enzyme. The results presented here indicate that copper is not
necessary or sufficient for catalysis and that copper addition to ACS is deleterious.
Several proposed mechanisms exist for the synthesis of acetyl-CoA, the two most
prominent are the Âparamagnetic and Âdiamagnetic mechanisms. The ÂdiamagneticÂ
mechanism proposes a two electron activation that precedes methylation to produce an
EPR silent Ni2+-CH3 species. This then reacts with CO and coenzyme-A to form acetyl-
CoA and regenerate the starting species. The Âparamagnetic mechanism assumes a one
electron activation prior to the methylation of the paramagnetic Ni1+-CO state to form an
unstable Ni3+-acetyl species. This is immediately reduced by an electron shuttle.
Results are presented here that no shuttle or external redox mediator is necessary for
catalysis. This supports the Âdiamagnetic mechanism, specifically that a two-electron
reductive activation is necessary and that the Ni1+-CO species is not an intermediate.
The two-electron reductive activation required by the Âdiamagnetic mechanism
results in an unknown electronic state. Two proposals have been made to describe this
form of the A-cluster. The first hypothesis from Brunold et al involves a one-electron
reduction of the [Fe4S4]2+ cube and a one-electron reduction of the Nip
2+. This should
result in a spin-coupled state that is S = integer. The Ni0 hypothesis requires both
electrons to localize on the Nip
2+ forming a zero-valent proximal nickel. Mössbauer
spectroscopy has been used to probe the oxidation state and spin state of the [Fe4S4] cube
in the reduced active form. No integer spin system is found and this is interpreted as
supporting the Ni0 hypothesis. Additionally, spectra are presented that indicate the
heterogeneous nature of the A-cluster is not caused by the occupancy of the proximal
site.
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The development of N2S2 metal complexes as bidentate ligands for organometallic chemistryRampersad, Marilyn Vena 25 April 2007 (has links)
Electronic and steric parameters for square planar NiN2S2 complexes as bidentate, S-donor ligands have been established. According to the (CO) stretching frequencies and associated computed Cotton-Kraihanzel force constants of (NiN2S2)W(CO)4 adducts, a ranking of donor abilities and a comparison with classical bidentate ligands are as follows: Ni(ema)= > { [NiN2S2]0 } > bipy phen > Ph2PCH2CH2PPh2 > Ph2PCH2PPh2. In addition, we have demonstrated that the NiN2S2 ligands are hemilabile as evidenced from CO addition to (NiN2S2)W(CO)4, which is in equilibrium with the resulting (NiN2S2)W(CO)5 species (Keq = 2.8 M-1, G = -1.4 kJ/mole at 50C). Complete NiN2S2 ligand displacement by CO-cleavage of the remaining W-S bond to form W(CO)6 was not observed, indicating that the remaining W-S bond is considerably strengthened upon ring-opening. Several new cluster compounds based on the NiN2S2 ligands bound to CuI, RhI, PdII and W0 are reported. Structural analysis of (NiN2S2)MLn complexes show a unique structural feature defined by the dihedral angle formed by the intersection of NiN2S2/WS2C2 planes; placing the NiN2S2 ligand in closer proximity to one side of the reactive metal center. This unique orientational feature of the NiN2S2 ligands in the series of bimetallic compounds contrasts with classical diphosphine or diimine ligands. The "hinge angle" ranges in value from 136 as in the (Ni-1*)W(CO)4 to 101 in the (Ni-1)Pd(CH3)(Cl) complexes. The rigidity of the SR hinge of the nickeldithiolate ligands suggests that they might be suitable for stereochemical and regioselective substrate addition to catalytically active metals such as RhI and PdII.. The structural as well as functional similarities of the acetyl CoA synthase enzyme (ACS) and a palladium-metal based industrial type catalyst led to the preparation of a [(Ni-1)Pd(CH3)]+ bimetallic complex. This complex facilitates CO and ethylene copolymerization to produce polyketone similar to conventional (diphosphine)Pd(X)2 catalysts. However, the diphosphine ligands produce more efficient catalysts as the electron-rich character of the NiN2S2 ligand favors the resting state of the catalyst, [(Ni-1)Pd(C(O)CH3)(CO)]+, over the reactive form (Ni-1)Pd(C(O)CH3)(2-C2H4)]+. An exploratory investigation with the Ni-Pd heterobimetallic showed that this complex also facilitated the C-S coupling reaction to form a thioester similar to the ACS enzyme.
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Ligand binding proteins: roles in ligand transfer and activation of nuclear receptorsPetrescu, Anca Daniela 30 September 2004 (has links)
Cholesterol and fatty acyl-coenzymeA thioesters are signalling molecules with role in regulation of genes involved in lipid and glucose transport and metabolism. The studies described herein focused on three proteins that bind lipids and have different cellular functions: steroidogenic acute regulatory protein (StAR), hepatocyte nuclear factor-4a (HNF-4a) and acyl-CoA binding protein (ACBP). First, StAR mediates delivery of cholesterol to inner mitochondrial membrane in steroidogenesis by a poorly understood mechanism. In our studies, fluorescent NBD-cholesterol binding assays demonstrate that StAR binds cholesterol at two binding sites with 32 nM Kds and circular dichroism spectra show that cholesterol binding results in changes of StAR secondary structure. Fluorescent sterol exchange assays between donor and acceptor mitochondrial membranes indicate that StAR significantly increased the formation of rapidly transferable cholesterol domains. Second, HNF-4a, a nuclear receptor, had been shown to bind fatty acyl-CoAs as natural ligands with apparent low affinities obtained with radiolabeled ligand binding assays. Our fluorescence spectroscopy studies demonstrate that HNF-4a ligand binding domain (HNF-4aLBD) binds acyl-CoAs at a single binding site with Kds of 1.6-4 nM. Fluorescence resonance energy transfer (FRET) between HNF-4aLBD tryptophan residues and cis-parinaroyl-CoA yielded an intermolecular distance of 42 Â thus pointing to direct molecular interaction. Third, although ACBP has been detected in the nucleus, it is not known whether ACBP may directly and/or functionally interact with a nuclear acyl-CoA binding protein such as HNF-4a to regulate transcription. Our present studies in vitro and in intact cultured cells, including circular dichroism of HNF-4a in the presence of ACBP, coimmunoprecipitation of HNF-4a/ACBP complexes, ACBP and HNF-4a colocalization in nuclei of cells by confocal microscopy demonstrate a physical association of ACBP and HNF-4a. FRET microscopy data indicated an intermolecular distance of 53 Â between ACBP and HNF-4a in rat hepatoma cells. Functional assays (transactivation of an HNF4a-dependent reporter gene) showed significant increase in the presence of ACBP in two different cell lines. Expression of ACBP anti-sense RNA decreased HNF-4a-mediated transactivation, pointing to a role of ACBP in co-regulating HNF-4a-dependent transcription.
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Untersuchungen zum Fettsäuretransport durch zelluläre und peroxisomale Membranen / Investigation of fatty acid transport across cellular and peroxisomal membranesScharnewski, Michael 19 January 2010 (has links)
No description available.
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Saturated and monounsaturated fatty acids differentially regulate adipokine gene expression and are associated with systemic C-Reactive Protein levels.Stryjecki, Carolina 14 September 2011 (has links)
This thesis investigates the contributions of fatty acids (FA) to adipokine dysregulation and inflammation. Differentiated 3T3-L1 adipocytes were treated with palmitic, stearic, palmitoleic, and oleic acids and changes in adipokine gene expression were measured. Here it was determined that saturated FA (SFA) increased the expression of RANTES and monounsaturated FA (MUFA) decreased the expression of RANTES and IL-6; demonstrating that FA differentially regulate adipokine expression. Relationships between plasma levels of SFA, MUFA and C-reactive protein (CRP) were also identified in a human observational study, further demonstrating the link between FA and inflammation Moreover, an association was also found between stearoyl-CoA desaturase 1 (SCD1) activity and CRP, demonstrating that SCD1 activity contributes to the inflammatory state. Genetic variation in SCD1 was also found to alter plasma FA and CRP levels, thus contributing to systemic inflammation. Taken together, these results demonstrate that SFA and MUFA influence adipokine dysregulation and systemic inflammation.
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Role of cytosolic acyl-CoA binding protein in seed oil biosynthesisYurchenko, Olga Unknown Date
No description available.
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Role of cytosolic acyl-CoA binding protein in seed oil biosynthesisYurchenko, Olga 11 1900 (has links)
Acyl-CoA binding protein (ACBP) ubiquitously found in eukaryotic organisms fulfills important functions of solubilisation, protection and transport of acyl-CoA esters, a major intermediate of lipid metabolism. This thesis presents an investigation of the physiological role of the small cytosolic ACBP in seed oil biosynthesis. The second important objective of this study was to evaluate the use of ACBP as a molecular tool for modification of seed oil content and/or fatty acid (FA) composition. Agrobacterium-mediated transformation of Arabidopsis thaliana and Brassica napus was performed with a number of genetic constructs designed for seed-specific expression of the B. napus cDNA encoding a small cytosolic ACBP. Protein level and subcellular localization of BnACBP in A. thaliana transgenic seeds depended on the structure of the genetic constructs mainly, the presence of additional in-frame sequences, encoding a protein fusion partners or signal peptides. Seed oil from A. thaliana T2 and T3 seeds had increased polyunsaturated fatty acid (PUFA) percentage (18:2cis delta9,12 and, in some lines, 18:3cis delta9,12,15) at the expense of very-long-chain monounsaturated (20:1cis delta11) and saturated (18:0) fatty acids. An increase in PUFA levels in seed oil was due to enhanced acyl channeling from the acyl-CoA pool to phosphatidylcholine, the substrate for extraplastidial FA desaturation. The activity of A. thaliana acyl-CoA: lysophosphatidylcholine acyltransferase (AthLPCAT), an enzyme involved in acyl exchange between acyl-CoA and PC, was significantly increased in the presence of the recombinant B. napus ACBP (rBnACBP) in the reaction mixture. rBnACBP also modulated enzymatic activities of glycerol-3-phosphate acyltransferase and diacylglycerol acyltransferase in vitro. Finally, the effect of constitutive or seed-specific gene silencing of ACBP on seed oil formation was examined. A. thaliana transformation with RNAi constructs resulted in partial suppression of ACBP expression and changes in FA composition of seed oil which included an increase in the percentage of 18:1cis delta9 and 18:2cis delta9,12 and, decrease of 18:3cis delta9,12,15. Overall, the results of this study demonstrate that the small cytosolic ACBP plays an important role in acyl exchange between acyl-CoA and PC metabolic pools. Overexpression of ACBP during seed development can be useful in genetic engineering strategies aimed at modifying the FA composition of seed oils. / Plant Science
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Acyl-CoA thioesterases - auxiliary enzymes in peroxisomal lipid metabolism /Westin, Maria A.K., January 2007 (has links)
Diss. (sammanfattning) Stockholm : Karolinska institutet, 2007. / Härtill 4 uppsatser.
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Genetic markers of neurodegeneration a role for 3-hydroxy-3-methylglutaryl-coenzyme A reductase in sporadic Alzheimer's disease /Legault, Véronique. January 1900 (has links)
Thesis (M.Sc.). / Written for the Dept. of Neurology and Neurosurgery. Title from title page of PDF (viewed 2008/05/14). Includes bibliographical references.
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Occupancy and function of the hepatic HMG-CoA reductase promoterLagor, William Raymond. January 2006 (has links)
Dissertation (Ph.D.)--University of South Florida, 2006. / Includes vita. Includes bibliographical references. Also available online.
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