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BASES FOR BREADTH - INSIGHTS INTO HOW THE MECHANISM AND DYNAMICS OF NITROREDUCTASE CAN EXPLAIN THIS ENZYME'S BROAD SUBSTRATE REPERTOIREPitsawong, Warintra 01 January 2014 (has links)
Nitroreductase from Enterobacter cloacae (NR) is a member of a large family of homologues represented in all branches of the tree of life. However the physiological roles of many of these enzymes remain unknown. NR has distinguished itself on the basis the diverse sizes and chemical types of substrates it is able to reduce (Koder et al 1998). This might be an evolved characteristic suiting NR for a role in metabolism of diverse occasional toxins. While there are numerous studies of determinants of substrate specificity, we know less about mechanisms by which enzymes can be inclusive. Therefore, we present a synthesis of NR's dynamics, stability, ligand binding repertoire and kinetic mechanism. We find that NR reduces para-nitrobenzoic acid (p-NBA) via a simple mechanism limited by the chemical step in which the nitro group is reduced (Pitsawong et al 2014). Thus, for this substrate, NR's mechanism dispenses with gating steps that in other enzymes can enforce substrate specificity. Our data demonstrate that substrate reduction is accomplished by rate-contributing hydride transfer from the flavin cofactor coupled to proton transfer from solvent, but do not identify specific amino acids with a role. This is consistent with our crystal structures, which reveal a spacious solvent-exposed active site bounded by a helix that moves to accommodate binding of substrate analogs (Haynes et al 2002). Because it is able to reduce TNT (trinitrotoluene), herbicides and pesticides, NR has important potential utility in bioremediation.
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Structural and functional characterization of a hybrid benzoate degradation pathwayBains, Jasleen 25 October 2011 (has links)
Aromatic compounds comprise approximately one quarter of the Earth's biomass and thus play a critical role in the biogeochemical carbon cycle. These compounds are degraded almost exclusively by specialized microbial enzymes that are part of complex metabolic pathways. Detailed characterization of these enzymes is both a gateway to understanding a biological process fundamental to nature and a platform for bioengineering applications in bioremediation. Recently, a novel pathway was shown to metabolize two key aromatic intermediates: Benzoate and Benzoyl-Coenzyme A. Designated as the box pathway (benzoate oxidation), this metabolic conduit incorporates in succession; CoA-ligation, oxygenation, ring cleavage and neutralization of the aldehydic ring cleavage product, catalyzed by a Benzoate Coenzyme A Ligase (BCL), BoxAB, BoxC and an Aldehyde Dehydrogenase (ALDH) respectively. Collectively, these steps define the initial and unique segment of the box pathway. The objective of the research described here was to establish a molecular blueprint of the substrate binding pocket of the initial BCL and elucidate mechanistic details for both BoxC and ALDH enzymes from Burkholderia xenovorans LB400 through in-depth structural and functional characterizations.
An intriguing feature of the box pathway in LB400 is a paralogous genetic organization. Functional studies on the BCL paralogs (BCLM and BCLC) show that BCLM is more active towards benzoate than BCLC. Structural analysis of the 1.84 Å resolution co- crystal structure of BCLM with benzoate reveals that the substrate binding pocket is closely contoured to bind benzoate, leaving little room to accommodate substituted benzoates, especially in the para position owing to a histidine (H339) residue that renders the pocket particularly shallow. Overall, while corroborative, the structural data provides a molecular rationale to our functional data where both the BCLs were seen to be highly specific for benzoate. Structural analysis of the 1.5 Å resolution crystal structure of the novel ring cleaving BoxC reveals an intriguing structural demarcation consistent with the primary sequence based divergence of BoxC within the crotonase superfamily. A highly divergent region in the C-terminus likely serves as a structural scaffold for the conserved N-terminus that harbors the active site. Isothermal titration calorimetry and molecular docking simulations contribute to a detailed view of the active site resulting in a compelling mechanistic model involving a pair of conserved glutamates (E146 and E168) and a novel cysteine (C111). Lastly, the 1.6 Å resolution co-crystal structure of ALDHC with NADPH and PEG allows identification of residues that are involved in rendering ALDHC selective for NADP+ and linear, medium to long chain aldehydes, as observed in our initial kinetic analyses. Functional and structural characterization of strategic ALDHC mutants enables us to propose a detailed reaction mechanism which involves the essential roles for C296 as the nucleophile, E257 as the general base and a proton relay network anchored by E496 and supported by E167 and K168. Overall, this research provides a molecular blueprint for three key box enzymes, thereby enhancing our understanding of central aromatic metabolism. / Graduate
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Investigation Of Cytocidal Effect Of K5 Type Yeast Killer Protein On Sensitive Microbial CellsSertkaya, Abdullah 01 September 2005 (has links) (PDF)
Some yeasts secrete polypeptide toxins, which are lethal to other sensitive yeast cells, gram-positive pathogenic bacteria and pathogenic fungi. Therefore these are designated as killer toxins. Killer toxins are suggested as potent antimicrobial agents especially for the protection of fermentation process against contaminating yeasts, biological control of undesirable yeasts in the preservation of foods. Moreover they are promising antimicrobial agents in the medical field / due to immune system suppressing diseases like AIDS, there is an increase in the incidence of fungal diseases and current antimycotics have low selectivity and severe side effects.
In this study our aim was to explain the cytocidal effect and enzymatic properties of K5 type yeast killer protein, which is secreted by Pichia anomala NCYC 434 cells, and known to have a broad range of killing spectrum. Competitive inhibition of the toxin with cell wall polysaccharides showed that primary binding site of toxin is & / #946 / -1,3-glucans of sensitive cells. Toxin showed exo-& / #946 / -1,3-glucanase activity which causes loss of cell wall rigidity leading cell death. Km and Vmax were found to be 0,3 mg/ml and 372,3 µ / mol/min/mg for laminarin hydrolysis. The toxin exerted its cytocidal effect after 2 h contact with the target cells. Toxin production was found to be dependent on & / #946 / -1,3-glucan content of the media. Toxin activity was completely inhibited by Hg+2 ,while several metal ions and DTT increased the activity to different extends. Our findings revealed the characteristics of K5 type killer toxin which will help for its possible uses in near future.
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Development of Au-immobilized P450 platform for exploring the effect of oligomer formation on P450-mediated metabolism for In vitro to In vivo drug metabolism predictionsKabulski, Jarod L. January 2010 (has links)
Thesis (Ph. D.)--West Virginia University, 2010. / Title from document title page. Document formatted into pages; contains xiv, 180 p. : ill. (some col.). Includes abstract. Includes bibliographical references.
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Estudos da correlação estrutura-função da enzima Clorocatecol 1,2-Dioxigenase de Pseudomonas putida / Studies of the structure-function correlation of the chlorocatechol 1,2-dioxygenase enzyme from Pseudomonas putidaNathalya Cristina de Moraes Roso Mesquita 13 February 2012 (has links)
O intenso uso de compostos orgânicos em conjunto com o grande avanço industrial culminou em um enorme acúmulo de poluentes orgânicos no meio ambiente. Dentre estes poluentes têm-se destacado a presença de hidrocarbonetos aromáticos altamente tóxicos e resistentes à degradação física, química, fotolítica e biológica. Desta maneira, uma nova forma de combater a presença deste tipo de composto no meio ambiente têm sido estudada: o uso de microorganismos, naturais ou geneticamente modificados, capazes de transformá-los em substâncias inertes, como CO2 e água. Tal metodologia é denominada biorremediação. Dentres estes microorganismos destacam-se bactérias dos gêneros Pseudomonas, Aeromonas, Beijerinckia, dentre outros, que têm sido estudadas para esta finalidade. A enzima clorocatecol 1,2-dioxigenase (Pp 1,2-CCD) é uma das proteínas expressas por bactérias do gênero Pseudomonas putida, sendo responsável pela clivagem de hidrocarbonetos aromáticos através da incorporação de ambos os átomos de uma molécula de oxigênio à estrutura do anel aromático, sendo a proteína escolhida para desenvolvermos o presente trabalho. Mais especificamente, nos interessa estudar como o mecanismo de ação da referida enzima é controlado por moléculas extrínsecas, como fosfolipídios. Tal interesse pela interação entre a enzima e fosfolipídios surgiu recentemente quando da obtenção da primeira estrutura cristalográfica de uma enzima da família da CCD (dioxigenases intradióis). Nesta estrutura foi observado um sítio de ligação por monômero para fosfolipídios, o que fez com que várias questões relativas à influência desses sobre a atividade da enzima fossem levantadas. Nosso objetivo foi fazer uso das técnicas de Dicroísmo Circular (CD), Calorimetria e Ressonância Paramagnética Eletrônica (RPE) para estudar alterações conformacionais da enzima e de sua cinética induzidas por moléculas de fosfolipídio, e assim, obter informações que correlacionem as mudanças estruturais com o mecanismo de atividade enzimática da enzima. Os resultados obtidos através do uso daquelas técnicas em conjunto com protocolos que possibilitam a delipidação da enzima mostraram que a presença do fosfolipídios na estrutura da enzima tem influência sobre a atividade enzimática. Quando retiramos o fosfolipídio/ácido graxo, pudemos visualizar uma pequena mudança na estrutura secundária da enzima, um aumento da entalpia de reação, bem como um aumento na velocidade de reação, enquanto que a afinidade da enzima pelo substrato diminuiu. Pudemos também observar uma maior estabilidade térmica da enzima quando na ausência do fosfolipídio/ácido graxo e não foi observado interação da Pp 1,2-CCD com modelos micelares constituídos por lisofosfolipídios. Um breve estudo realizado sobre o papel da força iônica na atividade e na estabilidade térmica da proteína mostrou que na ausência de NaCl, em pH 8, a enzima se mostrou mais ativa, com uma afinidade pelo substrato maior e neste ambiente com baixa força iônica foi observado uma pequena interação da enzima com modelos micelares carregados negativamente. Assim, pudemos concluir que as moléculas anfipáticas, retiradas com os processos de delipidação, apesar de modificarem muito pouco a estrutura secundária da enzima, ainda assim instauram modificações na sua função de catálise do substrato catecol. Esta informação juntamente com os dados sobre inibição do processo reacional ocasionada pelo produto da reação formam um novo conjunto de dados que pode ser utilizado para se alcançar o objetivo mais geral de se controlar a atividade biológica da Pp 1,2-CCD. / The intensive use of organic compounds in conjunction with the industrial advances led to a huge accumulation of organic pollutants in the environment. Among these pollutants it has been noticed the presence of aromatic hydrocarbons that are highly toxic and resistant to physical, chemical and biological degradation. Thus, a new way to deal with the presence of this compounds in the environment has been studied: the use of microorganisms, natural or genetically modified, that can turn them into inert substances such as CO2 and water. This methodology is called bioremediation. Among those microorganisms, bacteria from the gender Pseudomonas, Aeromonas, Beijerinckia, among others, have been studied for this purpose. The enzyme chlorocatechol 1,2-dioxygenase (Pp 1,2-CCD) is one of the proteins expressed by Pseudomonas putida bacteria, being responsible for the cleavage of aromatic hydrocarbons through the incorporation of both atoms of a molecule of oxygen into the aromatic ring structure, being the protein chosen for investigation in this work. More specifically, we are interested in studying how the mechanism of action of this enzyme is controlled by extrinsic molecules such as phospholipids. The interest in the interaction between the enzyme and phospholipids arose recently when the first crystal structure of an enzyme of the intradiol dioxygenase family was reported. In this structure it was observed a binding site for a phospholipid per monomer, which raised many issues concerning its influence on the activity of the enzyme. Our goal was to use the techniques of Circular Dichroism (CD), calorimetry and Electron Magnetic Resonance (EMR) to study enzyme conformational changes and kinetics alterations induced by phospholipid molecules, thus gathering information on the structure-function correlation. The results obtained through those experimental techniques in conjunction with the use of protocols for protein delipidation showed that the presence of phospholipids/fatty acids in the structure of the enzyme play a role in enzyme activity. Upon removal of the phospholipid/fatty acids, we observed small changes in the secondary structure of the enzyme, an increase of the enthalpy of reactions as well as an increase in the reaction rate, whereas the affinity of the enzyme for the substrate decreased. We also observed a higher thermal stability of the Pp 1,2-CCD in the absence of the phospholipids/fatty acids, but no interaction was observed between the Pp 1,2-CCD and lysophospholipid micelles. A brief study of the function of ionic strength on the activity and thermal stability of the protein showed that in the absence of NaCl, at pH 8, the enzyme is more active, showing a greater affinity for the substrate and a low interaction was observed between Pp 1,2-CCD and negatively charged micelles. This information along with the data on the inhibition capacity of the reaction product are a new set of data that can be used to achieve the more general goal of controlling Pp 1,2-CCD biological activity.
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Hodnocení enzymové kinetiky několika potenciálních inhibitorů lidských proteáz cysteinového a serinového typu / Enzyme kinetic evaluation of several potential inhibitors of certain human cysteine and serine proteasesHympánová, Michaela January 2018 (has links)
IN ENGLISH Charles University Faculty of Pharmacy in Hradec Králové Department of Biological and Medical Sciences Supervisors: prof. Dr. Michael Gütschow RNDr. Klára Konečná, Ph.D. Candidate: Michaela Hympánová Title of the diploma thesis: Enzyme kinetic evaluation of several potential inhibitors of certain human cysteine and serine proteases Background Cysteine and serine proteases are enzymes involved in many physiological processes. The imbalance between them and their endogenous inhibitors is associated with various diseases such as cancer and osteoporosis. Synthetic inactivators could be useful in the treatment of these enzyme-mediated pathological conditions. Therefore, there are ongoing attempts to develop low-molecular weight inactivators for therapeutically relevant cysteine and serine proteases. In the course of this thesis, compounds synthesized in prof. Gütschow's group were investigated as potential inhibitors of selected human proteases. They belong to imidazole compounds derived from N-protected cyclohexylalanine, 2-phenyl-7,8-dihydroimidazo[1,2- a]pyrazin-6(5H)-one derivatives, ,-unsaturated peptidomimetic compounds, carbamates, an N,N-dibenzylcrotonamide derivatives and peptoides. Aims This diploma thesis has been focused on the evaluation of new potential inhibitors against...
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Mechanismus působení nepeptidových inhibitorů HIV proteasy / Mechanism of action of non-peptide inhibitors of HIV proteaseBegan, Jakub January 2011 (has links)
The inhibition of HIV-1 protease plays an important role in combating HIV. Nine HIV-1 protease inhibitors have been succesfully marketed for the treatment since 1995. However, their efficiencies decrease due to the resistance development. More potent compounds with novel structural motifs and mechanisms of action are therefore still needed. Several inhibitory compounds have been reported to bind to the protease at the loci different from the active site. Interestingly, darunavir, which is the last approved inhibitor with supposedly competitive mode of action, was also suggested to bind to the flap region of the protease. Two studies discussed this alternative binding mode based on the X-ray structural and kinetic analysis, respectively. Nevertheless, it is questionable, if such a mechanism is relevant also in physiological conditions or if it is only an artifact of crystallization. Another study provided a strong evidence for the alternative binding of darunavir to highly mutated HIV-1 protease. Based on thermodynamic analysis, it was shown that two molecules of darunavir bind to the protease dimer. Surprisingly, this observation was not confirmed by the X-ray structure analysis since the inhibitor was bound only within the active site. However, this protease variant was employed in further...
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IN VITRO AND IN VIVO KINETIC MODELING OF DIAZEPAM METABOLISMWang, Zeyuan, 0000-0003-4526-829X January 2021 (has links)
Drug metabolism plays an important role in drug absorption and drug elimination. Therefore, it is crucial to understand the mechanism and kinetics of drug metabolism by various drug-metabolizing enzymes (DMEs). Cytochrome P450 enzymes (CYPs) are responsible for the metabolism of more than 60% of the top 200 prescribed drugs. X-ray and NMR data of CYP enzyme suggest that relatively large and flexible active sites are capable of multi-substrate binding. Due to the multiple substrate-binding, CYP reactions tend to show non-Michaelis Menten kinetics (atypical kinetics), multiple metabolite formation and sequential metabolism.To investigate the complexity of cytochrome P450 kinetics, saturation curves and intrinsic clearances (CLint) were simulated for single substrate and multi-substrate models using rate equations and numerical analysis. These models were combined with multiple product formation and sequential metabolism and simulations were performed with
random error. All simulation and model fitting was performed using Mathematica. A concentration-dependent metabolite ratio plot can be observed from multi-substrate binding kinetics. Use of single substrate models to characterize multi-substrate data can result in inaccurate kinetic parameters and poor clearance predictions. It has been shown that use of different substrate concentrations may lead to highly variable in vitro CLint estimations when sigmoidal kinetics are observed. Comparing results for use of standard velocity equations with ordinary differential equations (ODEs) clearly shows that ODEs are more versatile and provide better parameter estimates. It would be difficult to derive
concentration-velocity relationships for complex models, but these relationships can be easily modeled using numerical methods and ODEs.
The model drug diazepam (DZP) was chosen as the probe substrate to demonstrate complex CYP kinetics with specific CYP enzyme sources, including rat liver microsome (RLM), human liver microsome (HLM), purified CYP enzyme isoforms and rat hepatocytes. All saturation curves display non-Michaelis-Menten kinetics, form multiple primary metabolites, and are sequentially metabolized to secondary metabolites. In addition, the sequential metabolism and disposition would be characterized in hepatocytes incubation under flow conditions. To provide in vivo evidence of the atypical kinetics and investigate CYP-mediated sequential metabolism, preliminary intravascular (IV) dosing PK studies with male rats was performed for DZP. In general, DZP and its metabolites were quantitated by LC/MS/MS. Numerical methods were used to solve ODEs and parameterize micro and macro rate constants for the models. It has been shown that more complex models that include explicit enzyme-product complexes can well characterize the datasets for diazepam sequential metabolism with CYP3A4. Uncommon DZP metabolite PK profiles are observed in rat PK studies.
In summary, methods of in vitro data analysis are compared, new assays are developed, and new modeling approaches for complex drug and metabolite pharmacokinetics are being investigated. / Pharmaceutical Sciences
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Organic Phase Entrapment of Glucose Oxidase In Polymeric NanoparticlesHancock, James 12 May 2008 (has links)
No description available.
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Levodopa Drug Induced Alteration of Thiol Homeostasis in Model Neurons Activates Apoptosis Signaling Kinase 1: Implications for the Treatment of Parkinson's DiseaseSabens, Elizabeth Ann January 2010 (has links)
No description available.
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