ABSTRACT A core tool of sensory science is the use of trained descriptive panels. This research describes an investigation into the role of motivation in the performance of trained panels and the use of a trained panel to develop a better understanding of the perception of Sauvignon blanc wines. Substantial investment in time and money is directed towards ensuring trained panels perform optimally. Having selected a panel, the panel leader needs to ensure that panellists provide accurate, reliable data. Panellist motivation is also an important factor to consider. While performance psychology, education and sport science fields have researched motivation extensively, knowledge about panellist motivation within sensory science is limited. However, findings from existing research in these other areas - which suggest an important role for autonomy, competence and relatedness - can be applied to sensory panels in order to increase intrinsic motivation. The initial part of the research investigated the fundamental factors that affect and influence panellists’ motivation and participation. A survey (n=74) revealed that extra income and a general interest in food were the key drivers in inspiring people to become panellists, whilst enjoyment in being a panellist, interest in food, and extra income were key drivers for people to remain panellists. In a second survey, the intrinsic motivation of seven trained panels from four countries (n=108) was assessed. External panels were found to be more intrinsically motivated than internal panels. Experienced panellists had an increased perception of competence, which is a key factor for people to be intrinsically motivated. Understanding motivational frameworks currently used in other research fields and integrating them into existing panel training protocols may enhance and sustain panellists’ intrinsic motivation. A trained panel (n=14) was then used in the second part of the thesis to identify key flavours in Sauvignon blanc wines from Australia, France, New Zealand, Spain, South Africa and USA. Sixteen characteristics were identified and measured, including sweet sweaty passionfruit, capsicum, passionfruit skin/stalk, boxwood/cat’s urine, grassy, mineral/flinty, citrus, bourbon, apple lolly/candy, tropical, mint, fresh asparagus, canned asparagus, stonefruit, apple and snowpea. Principal component analysis was used to describe differences between regions and countries. Sauvignon blanc wines from Marlborough, New Zealand (NZ), were described by tropical and sweet sweaty passionfruit characteristics, while French and South African Sauvignon blanc wines were described as having flinty/mineral and bourbon-like flavors. Chemical analyses of these wines also showed that Marlborough, NZ wines had more methoxypyrazine and thiol compounds. A consumer study (n=109) showed that New Zealanders significantly prefer New Zealand style Sauvignon blanc. The final part of this research focused on using trained panellists to explore the interactions between volatile and non-volatile wine compounds and their effects on the aroma profile of New Zealand Sauvignon blanc wine. Four volatile aroma compounds that are important in New Zealand Sauvignon blanc wine were studied (isobutyl methoxypyrazine [MIBP], 3-mercaptohexanol [3MH], 3-mercaptohexanol acetate [3MHA], and ethyl decanoate). Each of these four aroma compounds were assessed in combination with three non-volatile polyphenolic compounds commonly found in Sauvignon blanc wine: catechin, caffeic acid and quercetin. Results showed each polyphenol had a unique effect when blended with a specific aroma compound, either suppressing, accentuating, or showing little effect on the perception of the aroma compounds. The perception of MIBP, 3MH, and ethyl decanoate were largely suppressed by the added polyphenols, with a few exceptions. The perception of 3MH was accentuated with the addition of caffeic acid, and the perception of 3MHA was accentuated with the addition of catechin. The interactive effects of aroma compounds with polyphenols likely reflect non-covalent associations in the wine solution that reduce the volatility of the aroma compounds. With an understanding of the interactive effects of volatile and non-volatile compounds in wine, winemakers might optimize the impact of selected volatile compounds by managing polyphenol levels, supporting their efforts to attain desirable wine aroma profiles.

The grape variety Sauvignon Blanc (SB) is the flagship of New Zealand’s wine industry and accounted for over 75 % of the value of total wine exports in 2008. Two volatile thiols, 3-mercaptohexan-1-ol (3MH) and 3-mercaptohexyl-acetate (3MHA), reminiscent of grapefruit and passion fruit respectively, are critical for the main varietal characters in New Zealand SB. These aromatic thiols are not present in the grape juice, but are synthesized and released by the yeast during alcoholic fermentation from non-aromatic precursors. The aim of this work was to elucidate the underlying genetics of volatile thiol synthesis in yeast (Saccharomyces cerevisiae) during alcoholic fermentation of grape juice. A gene-deletion strategy was chosen for the investigation of putative genes influencing 3MH and 3MHA release. The first part of this thesis optimized fermentation conditions in grape-juice-based media, which enabled auxotrophic laboratory strains, derived from S288C, to ferment grape juice to completion with high efficiency. Key steps to achieving this goal were the supplementation of the grape juice with higher than recommended amounts of amino acids, which increased the fermentation rate of auxotrophic yeast strains. Lysine auxotrophic strains especially benefited from this measure. In combination with the dilution of SB grape juice by 25 % with synthetic grape juice without sugars, the auxotrophic laboratory yeast BY4743 was able to metabolize all sugars in the grape juice-based media in a time frame similar to that of a commercial wine yeast. The key properties of the resulting wine were comparable to wine made with a commercial wine yeast under the same conditions. In the second part, these newly developed fermentation conditions were employed to screen 69 single-gene deletion strains in the laboratory yeast background BY4743. The list of the 69 candidate genes was compiled by combining existing knowledge about thiol production in yeast with the mining of several biological databases. Screening of the single-gene deletions revealed 17 genes which caused biologically relevant increases or decreases in volatile thiol production, but none abolished it. The majority of the 17 genes were related to the sulfur and nitrogen metabolism in yeast. A subset of these thiol-influencing genes were also deleted in a wine yeast, and were overexpressed in both wine yeast and laboratory yeast, to gain more insight in their regulatory effects. The findings confirmed that sulfur and nitrogen metabolism in yeast were important in regulating 3MH and 3MHA synthesis. Different sulfur and nitrogen sources were added to the grape must prior to fermentation and their effect on thiol release was studied. It was found that nitrogen sources urea and DAP, as well as, the sulfur compound S-ethyl-L-cysteine (SEC) increased 3MH and 3MHA concentrations in the resulting wines. The addition of cysteine to grape juice fermented with wine yeast deleted in genes CYS3 and CYS4 more than doubled total thiol production. Mapping approaches to investigate thiol production in yeast were employed in the final part of this thesis. Genetically mapped F2 progeny of a cross between a low thiol-producing yeast strain and a high-thiol producer were screened for their thiol phenotype. The 3MH and 3MHA phenotypes across 48 screened F2 progeny resembled normal distributions, indicating a quantitative trait. Subsequent mapping identified a locus on chromosome 14 with a small effect on the 3MHA phenotype, but no obvious candidate genes were evident in the region. Another approach to investigate the evolution of volatile thiols in yeast included the use of SEC, a thiol compound resembling the cysteinylated precursor of 3MH, as a sole nitrogen source in a yeast growth assay. It was found that most wine yeast, European yeast isolates and laboratory yeasts could utilize SEC as a nitrogen source, whereas various other S. cerevisiae isolates could not. Crosses between three pairs of Sec- and Sec+ yeast strains strongly indicated that this trait was monogenically inherited. However, no direct correlation between the SEC phenotype and volatile release could be observed. Genetic mapping experiments in one SEC-segregating yeast population linked this SEC phenotype to the leu2-D0 deletion in a cross between a Leu+ and Leu- yeast strain. It was shown that leucine auxotrophy most likely caused the Sec- phenotype. In a second F2 population of a cross between prototrophic Sec+ and Sec- strains, strong linkage was established to a region on chromosome 6 containing two candidate genes, DUG1 and IRC7. DUG1 was proved not to be the cause of the SEC phenotype, whereas IRC7 remains a strong candidate gene.

ABSTRACT A core tool of sensory science is the use of trained descriptive panels. This research describes an investigation into the role of motivation in the performance of trained panels and the use of a trained panel to develop a better understanding of the perception of Sauvignon blanc wines. Substantial investment in time and money is directed towards ensuring trained panels perform optimally. Having selected a panel, the panel leader needs to ensure that panellists provide accurate, reliable data. Panellist motivation is also an important factor to consider. While performance psychology, education and sport science fields have researched motivation extensively, knowledge about panellist motivation within sensory science is limited. However, findings from existing research in these other areas - which suggest an important role for autonomy, competence and relatedness - can be applied to sensory panels in order to increase intrinsic motivation. The initial part of the research investigated the fundamental factors that affect and influence panellists’ motivation and participation. A survey (n=74) revealed that extra income and a general interest in food were the key drivers in inspiring people to become panellists, whilst enjoyment in being a panellist, interest in food, and extra income were key drivers for people to remain panellists. In a second survey, the intrinsic motivation of seven trained panels from four countries (n=108) was assessed. External panels were found to be more intrinsically motivated than internal panels. Experienced panellists had an increased perception of competence, which is a key factor for people to be intrinsically motivated. Understanding motivational frameworks currently used in other research fields and integrating them into existing panel training protocols may enhance and sustain panellists’ intrinsic motivation. A trained panel (n=14) was then used in the second part of the thesis to identify key flavours in Sauvignon blanc wines from Australia, France, New Zealand, Spain, South Africa and USA. Sixteen characteristics were identified and measured, including sweet sweaty passionfruit, capsicum, passionfruit skin/stalk, boxwood/cat’s urine, grassy, mineral/flinty, citrus, bourbon, apple lolly/candy, tropical, mint, fresh asparagus, canned asparagus, stonefruit, apple and snowpea. Principal component analysis was used to describe differences between regions and countries. Sauvignon blanc wines from Marlborough, New Zealand (NZ), were described by tropical and sweet sweaty passionfruit characteristics, while French and South African Sauvignon blanc wines were described as having flinty/mineral and bourbon-like flavors. Chemical analyses of these wines also showed that Marlborough, NZ wines had more methoxypyrazine and thiol compounds. A consumer study (n=109) showed that New Zealanders significantly prefer New Zealand style Sauvignon blanc. The final part of this research focused on using trained panellists to explore the interactions between volatile and non-volatile wine compounds and their effects on the aroma profile of New Zealand Sauvignon blanc wine. Four volatile aroma compounds that are important in New Zealand Sauvignon blanc wine were studied (isobutyl methoxypyrazine [MIBP], 3-mercaptohexanol [3MH], 3-mercaptohexanol acetate [3MHA], and ethyl decanoate). Each of these four aroma compounds were assessed in combination with three non-volatile polyphenolic compounds commonly found in Sauvignon blanc wine: catechin, caffeic acid and quercetin. Results showed each polyphenol had a unique effect when blended with a specific aroma compound, either suppressing, accentuating, or showing little effect on the perception of the aroma compounds. The perception of MIBP, 3MH, and ethyl decanoate were largely suppressed by the added polyphenols, with a few exceptions. The perception of 3MH was accentuated with the addition of caffeic acid, and the perception of 3MHA was accentuated with the addition of catechin. The interactive effects of aroma compounds with polyphenols likely reflect non-covalent associations in the wine solution that reduce the volatility of the aroma compounds. With an understanding of the interactive effects of volatile and non-volatile compounds in wine, winemakers might optimize the impact of selected volatile compounds by managing polyphenol levels, supporting their efforts to attain desirable wine aroma profiles.

The grape variety Sauvignon Blanc (SB) is the flagship of New Zealand’s wine industry and accounted for over 75 % of the value of total wine exports in 2008. Two volatile thiols, 3-mercaptohexan-1-ol (3MH) and 3-mercaptohexyl-acetate (3MHA), reminiscent of grapefruit and passion fruit respectively, are critical for the main varietal characters in New Zealand SB. These aromatic thiols are not present in the grape juice, but are synthesized and released by the yeast during alcoholic fermentation from non-aromatic precursors. The aim of this work was to elucidate the underlying genetics of volatile thiol synthesis in yeast (Saccharomyces cerevisiae) during alcoholic fermentation of grape juice. A gene-deletion strategy was chosen for the investigation of putative genes influencing 3MH and 3MHA release. The first part of this thesis optimized fermentation conditions in grape-juice-based media, which enabled auxotrophic laboratory strains, derived from S288C, to ferment grape juice to completion with high efficiency. Key steps to achieving this goal were the supplementation of the grape juice with higher than recommended amounts of amino acids, which increased the fermentation rate of auxotrophic yeast strains. Lysine auxotrophic strains especially benefited from this measure. In combination with the dilution of SB grape juice by 25 % with synthetic grape juice without sugars, the auxotrophic laboratory yeast BY4743 was able to metabolize all sugars in the grape juice-based media in a time frame similar to that of a commercial wine yeast. The key properties of the resulting wine were comparable to wine made with a commercial wine yeast under the same conditions. In the second part, these newly developed fermentation conditions were employed to screen 69 single-gene deletion strains in the laboratory yeast background BY4743. The list of the 69 candidate genes was compiled by combining existing knowledge about thiol production in yeast with the mining of several biological databases. Screening of the single-gene deletions revealed 17 genes which caused biologically relevant increases or decreases in volatile thiol production, but none abolished it. The majority of the 17 genes were related to the sulfur and nitrogen metabolism in yeast. A subset of these thiol-influencing genes were also deleted in a wine yeast, and were overexpressed in both wine yeast and laboratory yeast, to gain more insight in their regulatory effects. The findings confirmed that sulfur and nitrogen metabolism in yeast were important in regulating 3MH and 3MHA synthesis. Different sulfur and nitrogen sources were added to the grape must prior to fermentation and their effect on thiol release was studied. It was found that nitrogen sources urea and DAP, as well as, the sulfur compound S-ethyl-L-cysteine (SEC) increased 3MH and 3MHA concentrations in the resulting wines. The addition of cysteine to grape juice fermented with wine yeast deleted in genes CYS3 and CYS4 more than doubled total thiol production. Mapping approaches to investigate thiol production in yeast were employed in the final part of this thesis. Genetically mapped F2 progeny of a cross between a low thiol-producing yeast strain and a high-thiol producer were screened for their thiol phenotype. The 3MH and 3MHA phenotypes across 48 screened F2 progeny resembled normal distributions, indicating a quantitative trait. Subsequent mapping identified a locus on chromosome 14 with a small effect on the 3MHA phenotype, but no obvious candidate genes were evident in the region. Another approach to investigate the evolution of volatile thiols in yeast included the use of SEC, a thiol compound resembling the cysteinylated precursor of 3MH, as a sole nitrogen source in a yeast growth assay. It was found that most wine yeast, European yeast isolates and laboratory yeasts could utilize SEC as a nitrogen source, whereas various other S. cerevisiae isolates could not. Crosses between three pairs of Sec- and Sec+ yeast strains strongly indicated that this trait was monogenically inherited. However, no direct correlation between the SEC phenotype and volatile release could be observed. Genetic mapping experiments in one SEC-segregating yeast population linked this SEC phenotype to the leu2-D0 deletion in a cross between a Leu+ and Leu- yeast strain. It was shown that leucine auxotrophy most likely caused the Sec- phenotype. In a second F2 population of a cross between prototrophic Sec+ and Sec- strains, strong linkage was established to a region on chromosome 6 containing two candidate genes, DUG1 and IRC7. DUG1 was proved not to be the cause of the SEC phenotype, whereas IRC7 remains a strong candidate gene.

ABSTRACT A core tool of sensory science is the use of trained descriptive panels. This research describes an investigation into the role of motivation in the performance of trained panels and the use of a trained panel to develop a better understanding of the perception of Sauvignon blanc wines. Substantial investment in time and money is directed towards ensuring trained panels perform optimally. Having selected a panel, the panel leader needs to ensure that panellists provide accurate, reliable data. Panellist motivation is also an important factor to consider. While performance psychology, education and sport science fields have researched motivation extensively, knowledge about panellist motivation within sensory science is limited. However, findings from existing research in these other areas - which suggest an important role for autonomy, competence and relatedness - can be applied to sensory panels in order to increase intrinsic motivation. The initial part of the research investigated the fundamental factors that affect and influence panellists’ motivation and participation. A survey (n=74) revealed that extra income and a general interest in food were the key drivers in inspiring people to become panellists, whilst enjoyment in being a panellist, interest in food, and extra income were key drivers for people to remain panellists. In a second survey, the intrinsic motivation of seven trained panels from four countries (n=108) was assessed. External panels were found to be more intrinsically motivated than internal panels. Experienced panellists had an increased perception of competence, which is a key factor for people to be intrinsically motivated. Understanding motivational frameworks currently used in other research fields and integrating them into existing panel training protocols may enhance and sustain panellists’ intrinsic motivation. A trained panel (n=14) was then used in the second part of the thesis to identify key flavours in Sauvignon blanc wines from Australia, France, New Zealand, Spain, South Africa and USA. Sixteen characteristics were identified and measured, including sweet sweaty passionfruit, capsicum, passionfruit skin/stalk, boxwood/cat’s urine, grassy, mineral/flinty, citrus, bourbon, apple lolly/candy, tropical, mint, fresh asparagus, canned asparagus, stonefruit, apple and snowpea. Principal component analysis was used to describe differences between regions and countries. Sauvignon blanc wines from Marlborough, New Zealand (NZ), were described by tropical and sweet sweaty passionfruit characteristics, while French and South African Sauvignon blanc wines were described as having flinty/mineral and bourbon-like flavors. Chemical analyses of these wines also showed that Marlborough, NZ wines had more methoxypyrazine and thiol compounds. A consumer study (n=109) showed that New Zealanders significantly prefer New Zealand style Sauvignon blanc. The final part of this research focused on using trained panellists to explore the interactions between volatile and non-volatile wine compounds and their effects on the aroma profile of New Zealand Sauvignon blanc wine. Four volatile aroma compounds that are important in New Zealand Sauvignon blanc wine were studied (isobutyl methoxypyrazine [MIBP], 3-mercaptohexanol [3MH], 3-mercaptohexanol acetate [3MHA], and ethyl decanoate). Each of these four aroma compounds were assessed in combination with three non-volatile polyphenolic compounds commonly found in Sauvignon blanc wine: catechin, caffeic acid and quercetin. Results showed each polyphenol had a unique effect when blended with a specific aroma compound, either suppressing, accentuating, or showing little effect on the perception of the aroma compounds. The perception of MIBP, 3MH, and ethyl decanoate were largely suppressed by the added polyphenols, with a few exceptions. The perception of 3MH was accentuated with the addition of caffeic acid, and the perception of 3MHA was accentuated with the addition of catechin. The interactive effects of aroma compounds with polyphenols likely reflect non-covalent associations in the wine solution that reduce the volatility of the aroma compounds. With an understanding of the interactive effects of volatile and non-volatile compounds in wine, winemakers might optimize the impact of selected volatile compounds by managing polyphenol levels, supporting their efforts to attain desirable wine aroma profiles.

The grape variety Sauvignon Blanc (SB) is the flagship of New Zealand’s wine industry and accounted for over 75 % of the value of total wine exports in 2008. Two volatile thiols, 3-mercaptohexan-1-ol (3MH) and 3-mercaptohexyl-acetate (3MHA), reminiscent of grapefruit and passion fruit respectively, are critical for the main varietal characters in New Zealand SB. These aromatic thiols are not present in the grape juice, but are synthesized and released by the yeast during alcoholic fermentation from non-aromatic precursors. The aim of this work was to elucidate the underlying genetics of volatile thiol synthesis in yeast (Saccharomyces cerevisiae) during alcoholic fermentation of grape juice. A gene-deletion strategy was chosen for the investigation of putative genes influencing 3MH and 3MHA release. The first part of this thesis optimized fermentation conditions in grape-juice-based media, which enabled auxotrophic laboratory strains, derived from S288C, to ferment grape juice to completion with high efficiency. Key steps to achieving this goal were the supplementation of the grape juice with higher than recommended amounts of amino acids, which increased the fermentation rate of auxotrophic yeast strains. Lysine auxotrophic strains especially benefited from this measure. In combination with the dilution of SB grape juice by 25 % with synthetic grape juice without sugars, the auxotrophic laboratory yeast BY4743 was able to metabolize all sugars in the grape juice-based media in a time frame similar to that of a commercial wine yeast. The key properties of the resulting wine were comparable to wine made with a commercial wine yeast under the same conditions. In the second part, these newly developed fermentation conditions were employed to screen 69 single-gene deletion strains in the laboratory yeast background BY4743. The list of the 69 candidate genes was compiled by combining existing knowledge about thiol production in yeast with the mining of several biological databases. Screening of the single-gene deletions revealed 17 genes which caused biologically relevant increases or decreases in volatile thiol production, but none abolished it. The majority of the 17 genes were related to the sulfur and nitrogen metabolism in yeast. A subset of these thiol-influencing genes were also deleted in a wine yeast, and were overexpressed in both wine yeast and laboratory yeast, to gain more insight in their regulatory effects. The findings confirmed that sulfur and nitrogen metabolism in yeast were important in regulating 3MH and 3MHA synthesis. Different sulfur and nitrogen sources were added to the grape must prior to fermentation and their effect on thiol release was studied. It was found that nitrogen sources urea and DAP, as well as, the sulfur compound S-ethyl-L-cysteine (SEC) increased 3MH and 3MHA concentrations in the resulting wines. The addition of cysteine to grape juice fermented with wine yeast deleted in genes CYS3 and CYS4 more than doubled total thiol production. Mapping approaches to investigate thiol production in yeast were employed in the final part of this thesis. Genetically mapped F2 progeny of a cross between a low thiol-producing yeast strain and a high-thiol producer were screened for their thiol phenotype. The 3MH and 3MHA phenotypes across 48 screened F2 progeny resembled normal distributions, indicating a quantitative trait. Subsequent mapping identified a locus on chromosome 14 with a small effect on the 3MHA phenotype, but no obvious candidate genes were evident in the region. Another approach to investigate the evolution of volatile thiols in yeast included the use of SEC, a thiol compound resembling the cysteinylated precursor of 3MH, as a sole nitrogen source in a yeast growth assay. It was found that most wine yeast, European yeast isolates and laboratory yeasts could utilize SEC as a nitrogen source, whereas various other S. cerevisiae isolates could not. Crosses between three pairs of Sec- and Sec+ yeast strains strongly indicated that this trait was monogenically inherited. However, no direct correlation between the SEC phenotype and volatile release could be observed. Genetic mapping experiments in one SEC-segregating yeast population linked this SEC phenotype to the leu2-D0 deletion in a cross between a Leu+ and Leu- yeast strain. It was shown that leucine auxotrophy most likely caused the Sec- phenotype. In a second F2 population of a cross between prototrophic Sec+ and Sec- strains, strong linkage was established to a region on chromosome 6 containing two candidate genes, DUG1 and IRC7. DUG1 was proved not to be the cause of the SEC phenotype, whereas IRC7 remains a strong candidate gene.

Este trabalho consistiu de estudos da viabilidade da geração e identificação de radicais livres envolvidos em processos oxidativos avançados por via eletroquímica. Para a geração e identificação de radicais livres em eletrodos modificados com organotióis via eletroquímica, escolheu-se uma técnica pouco aplicada para este fim; a espectroscopia de impedância eletroquímica, e o ajuste dos dados experimentais pela proposta de modelos de circuitos equivalentes. O eletrodo de trabalho utilizado (Au) foi caracterizado em meio ácido e básico e diversas monocamadas auto-organizadas conhecidas foram adsorvidas sobre o mesmo e também caracterizadas por esta técnica. Parâmetros importantes como constante dielétrica, capacitância de uma monocamada livre de defeitos e grau de recobrimento foram determinados com êxito. Também foram empregadas moléculas menos utilizadas como modificadoras de eletrodos (fenotiazinas e derivados). As mesmas foram caracterizadas no sistema Au/adsorvente/NaOH, pois, o pH alto garante a formação do radical superóxido e do ânion hidroperóxido. Os mesmos modelos de circuitos equivalentes puderam ser empregados na obtenção dos parâmetros físicos relativos a essas moléculas no sistema eletroquímico utilizado. Em uma etapa subsequente obteve-se a valiosa informação, se as moléculas adsorvidas sobre Au poderiam ser usadas para a geração de superóxido e outros radicais. As monocamadas de tióis, quando utilizadas para gerar radicais livres, se mostraram aptas a gerar superóxido em meio alcalino saturado com oxigênio molecular. Como se demonstrou na etapa de caracterização, as SAM-3 e SAM-6 não formaram um empacotamento totalmente hidrofóbico. Por este motivo, mesmo que superóxido tenha sido gerado, não pôde ser detectado. Já para a fenotiazina e seu metil-derivado, a cinética de adsorção e a utilização de soluções aquosas impediram a formação de um filme completo e homogêneo, imprescindível para a constituição de uma interface hidrofóbica e isolante. Além disso, possíveis reações de complexação entre as moléculas e superóxido, reações entre a fenotiazina cátion-radical e superóxido fazem necessários mais estudos acerca da natureza eletroquímica do sistema, que já é bastante conhecido fotoquimicamente. Posterior a modificação, todos os eletrodos se mostraram ser bastante sensíveis ao pH e aos eletrólitos utlizados, alterando-se a estrutura interna muito facilmente, o qual implica uma limitação no tempo de uso e reprodutibilidade quando da geração de um radical tão reativo quanto superóxido. / This work consisted in testing the viability of investigations into the electrochemical generation and identification of free radicals involved in advanced oxidative processes. In these studies, a technique which is rarely used for the electrochemical generation and identification of free radicals at organothiole-modified electrodes, electrochemical impedancy spectroscopy, was chosen and the experimental data obtained were fitted by equivalent circuit models. A working electrode (Au) was characterized in both acidic and basic media and several known self-assembled monolayers were adsorbed over this electrode and also characterized using this technique. Important parameters such as dielectric constants, capacitance of the monolayers free of defects and coverage were determined with success. Other lesser-known molecules such as phenothiazines and their derivatives were also used .The modified electrodes were characterized in NaOH solution, since the high pH assures the production of superoxide radicals and hydroperoxylate anions. The equivalent circuit model was employed to obtain physical parameters for these molecules in the electrochemical systems studied. In a subsequent step, a valuable piece of information was obtained; it was noted that the molecules adsorbed over Au could be used in order to generate superoxide and other radicals. The ability of thiol monolayers used in the generation of free radicals, to produce superoxides in alkaline media saturated with molecular oxygen was demonstrated. However, characterization of the self-assembled monolayers, SAM-3 and SAM-6, revealed that these were not able to pack in a completely hydrophobic manner. This may account for the fact that the superoxide could not be detected even when it was believed to have formed. For the phenothiazine-modified electrodes, the adsorption kinetics and the utilization of aqueous solutions prevented the formation of an intact and homogeneous film, which is essential in establishing a hydrophobic and isolating interface. Furthermore, possible complexation reactions between the molecules and the superoxide and reactions between the phenothiazine cation-radical and superoxide, point to the need for further studies regarding the electrochemical nature of this system, whose photochemical properties are very well known. Following modification, all the electrodes were shown to be too sensitive to pH and to the electrolytes used, since the inner structure was easily modified, which implies that they would have a limited time of use and in addition that the reproducibility of the rate of generation of reactive radical species such as superoxides could be compromised.

A reatividade das lupulonas, terpenos, flavonoides prenilados e compostos contendo grupos tióis livre foi avaliada frente ao radical 1-hidroxietila (HER) para melhor conhecer o balanço redox da cerveja. As constantes de velocidade aparentes (kap) para a reação entre HER e os substratos supracitados foram obtidas via cinética de competição utilizando a armadilha química 4-POBN como competidor e monitorando-se o aduto radical formado por RPE. A partir dos valores obtidos de kap (108 L mol-1 s-1 para as lupulonas, 105 a 107 L mol-1 s-1 para terpenos, 109 L mol-1 s-1 para os flavonoides prenilados, e 108 a 109 L mol-1 s-1 para tióis) e pelas concentrações médias destes compostos na cerveja, pôde-se inferir que a extensão da degradação térmica destes compostos na bebida aumenta na ordem: lupulonas > tióis > flavonoides prenilados > terpenos. Os produtos de reação foram identificados por espectrometria de massas, e através de investigações eletroquímicas e cálculos ab initio empregando-se DFT se propôs um mecanismo de reação. Os produtos de degradação pela reação com HER foram: derivados hidroxilados e compostos de adição do radical HER para as lupulonas; derivados hidroxilados para os terpenos; derivados de adição do radical HER para os flavonoides prenilados; e dissulfetos para os tióis. Em experimento similar foram determinadas as kap para a reação entre metil ésteres derivados de ácidos graxos insaturados e esteróis com o HER, cujos valores de kap variaram de (2,7 ± 0,1) x 107 até (5,2 ± 0,1) x 107 L mol-1 s-1 para o metil docosahexanoato e ergosterol, respectivamente. Os dados cinéticos aqui obtidos contribuem para um melhor conhecimento da degradação térmica oxidativa da cerveja, bem como sugerem que os polifenóis prenilados podem conferir um significativo efeito antioxidante ao organismo humano quando do seu consumo e absorção. / The reactivity of lupulones, terpenes, prenilated flavonoids and thiol-containing compounds was evaluated towards the 1-hydroxyethyl radical (HER) to provide a better knowledge of the redox balance of beer. The apparent rate constants (kap) for the reaction between HER and the substrates were obtained through a competitive kinetic approach using the spin-trap 4-POBN as a competitor and by monitoring the radical adduct by EPR. From the obtained values of kap (108 L mol-1 s-1 for lupulones, from 105 to 107 L mol-1 s-1 for terpenes, 109 L mol-1 s-1 for prenylated flavonoids, and from 108 to 109 L mol-1 s-1 thiol compounds) and the average concentrations of these compounds in beer, it is possible to infer that the extension of the thermal degradation on the beverage is enhanced according to: lupulones > thiol compounds > prenylated flavonoids > terpenes. The reaction products were identified by mass spectrometry, and by electrochemical investigations and ab initio (DFT) calculation, a reaction mechanism has been proposed. The degradation products for the reaction with HER were: hydroxide derivatives and HER addition products for the lupulones; hydroxide derivatives for terpenes; HER addition derivatives for prenylated flavonoids; and disulfides for thiol cmpounds. In similar experiments it was determined the kap for the reaction among methyl ester derivatives of unsaturated fatty acids and sterols with HER, with kap values ranging from (2.7 ± 0.1) x 107 to (5.2 ± 0.1) x 107 L mol-1 s-1 for the methyl docosahexanoate and ergosterol, respectively. The obtained kinetic data may contribute for a better knowledge of the thermal oxidative degradation of beer, as well as may suggest that prenylated polyphenols could present a significant antioxidant effect in the human body through its consumption and absorption.

Os ânions inorgânicos nitrato (NO3-) e nitrito (NO2-) por muito tempo foram considerados produtos finais inertes do metabolismo do óxido nítrico (NO) e constituintes indesejáveis da dieta. Entretanto, é crescente o interesse das potenciais reações que podem se processar em meio fisiológico e, que envolvem especialmente o íon nitrito mediadas por complexos de metais de transição. Ferro-heme presente em proteínas como a mioglobina podem formar complexos porfirínicos com NO, gerando espécies que podem atuar principalmente como catalisadores em diversas vias biológicos importantes. Complexos com NOx coordenado a ferro-heme estão envolvidos tanto no processo da cura da carne (pigmentação da carne), como em processos redox, nos quais são capazes de oxidar substratos indiretamente pela produção de espécies reativas ou diretamente por reações de transferência de átomo de oxigênio (TAO). Os lipídeos, constituintes celulares fundamentais na composição de membranas e lipoproteínas, podem servir como substratos para essas reações e, sua oxidação pode ocasionar danos ao organismo. Tióis, importantes antioxidantes e constituintes de proteínas, também podem participar desse tipo de reações e, conseqüentemente gerar danos ao organismo. Considerando que o mecanismo e os parâmetros cinéticos e termodinâmicos destas reações ainda não foram completamente estabelecidos para explicar a vasta funcionalidade destes complexos, o presente projeto de pesquisa visa proporcionar um melhor conhecimento das reações redox envolvendo NOx e mediadas por porfirinas de ferro em alimentos e sistemas biológicos. / For long time, the anions nitrate (NO3-) and nitrite (NO2-) were considered inert end products of nitric oxide (NO) metabolism and undesirable constituents of the diet. Currently, there is an increasing interest for potential reactions which may occur in physiological conditions involving specially the nitrite ion and mediated by transition metal complexes. Heme NOx iron complexes are involved in meat curing process (meat pigmentation) and are able to oxidize substrates indirectly generating reactive species or directly by oxygen atom transfer reactions (OAT). Lipids, fundamental cellular constituents of membranes and lipoproteins, and thiols, important antioxidants and protein constituents, may serve as substrates to OAT and their oxidation may promote damage to the organism Considering that the mechanism and kinetic and thermodinamic parameters of these reaction have not yet been fully elucidated to explain the varied functionality of these complexes, the present research project aim to bring a better understanding of redox reactions involving NOx mediated by iron porphyrins in foods and biological systems. Thiols, important antioxidants and protein constituents, may serve as substrates to OAT and their oxidation may promote damage to the organism. The present work aims to bring a better understanding of the mechanism, kinetic and thermodynamic parameters of the reaction involving nitrite mediated by iron-porphyrins in food and biological systems.

La vie a émergé sur Terre il y a probablement 3,8 milliards d'années, sur une planète largement recouverte d'eau. Ce travail porte sur la synthèse prébiotique de peptides, en particulier de peptides riches en thiol. Nous avons étudié les réactions des aminonitriles (les premiers produits de la réaction de Strecker) avec la cystéine et l'homocystéine. Elles conduisent à la formation de cycles à 5 ou 6 chaînons qui sont ensuite hydrolysés pour donner les dipeptides correspondants (aa-Cys ou aa-Hcy). Les dipeptides contenant un thiol obtenus sont capables de favoriser la formation de chaînes peptidiques plus longues via des liaisons thioesters et de favoriser la formation de certains hétérocycles. L'homocystéine nitrile se cyclise dans l'eau pour former l'homocystéine thiolactone, qui présente une double réactivité, la thiolactone est ouverte par des amines puis on observe une condensation de l'aminothiol ainsi formé avec les nitriles. Le nitrile de cystéine et le thioester de S-éthyle de la cystéine conduisent à la formation de polycystéine, tandis que les molécules de type Cys-aa-CN donnent des polypeptides linéaires et cycliques. Nos résultats soutiennent l’hypothèse que des peptides contenant des thiols auraient joué un rôle important dans les premiers stades du développement de la vie. / Life emerged on Earth probably about 3.8 billion years ago, on a planet that was largely covered by water. This work focuses on the prebiotic synthesis of peptides, especially thiol-rich ones. We studied the reactions of aminonitriles (the first products of the Strecker reaction) with cysteine and homocysteine. These reactions lead to the formation of 5- or 6-membered rings which are then hydrolysed to give the corresponding dipeptides (aa-Cys or aa-Hcy). The obtained thiol-containing dipeptides are able to promote the formation of longer peptide chains via thioesters bonds, and to promote the formation of some heterocycles. Homocysteine nitrile cyclizes in water to form homocysteine thiolactone, which shows a double reactivity, thiolactone opening by amines followed by aminothiol condensation reaction with nitriles. Cysteine nitrile and the S-ethyl thioester of cysteine lead to the formation of polycysteine, while Cys-aa-CN molecules gives linear and cyclic polypeptides. Our results support the hypothesis that thiol-containing peptides would have been important molecules in the early stages of life development.