The purpose of this study was to screen the effect of some food-grade ingredients on the off-odors caused by geosmin and 2-methylisoborneol (MIB) compounds in catfish fillets by sensory evaluation. The study revealed that geosmin and MIB odor intensity were reduced to different degrees when fillets were dipped in lime flavor (94% and 67%, respectively), 0.5% acetic acid (AA) (70% and 16%, respectively), hardwood liquid smoke (98% and 86%, respectively), or hickory liquid smoke (98% and 100% respectively) in cooked products. A 0.5% AA proved to be effective in decreasing odor intensity of geosmin (70%) in cooked products, whereas lime flavor (94%), hardwood liquid smoke (98%), and hickory liquid smoke (98%) were very effective in decreasing odor intensity of geosmin in cooked products. These agents added desirable flavors as well, except for AA by panelists? comments. These flavors could be added to a marinade or incorporated in an injection/tumbling solution when catfish fillets are processed.

Os produtos cárneos prontos para consumo estão entre os principais alimentos associados a surtos de listeriose, uma doença causada por Listeria monocytogenes. Este estudo objetivou avaliar a ação antimicrobiana do lactato de sódio e de duas formulações comerciais à base de nisina (produtos A e B) em mortadela, e do lactato de sódio e fumaça líquida em salsicha, experimentalmente contaminadas com um pool de seis cepas de L. monocytogenes, durante o armazenamento à vácuo à 8 ºC. Os aditivos com melhor atividade anti-listeria também foram avaliados quanto ao controle de bactérias láticas (BAL) e bolores e leveduras em produto cárneo, durante o armazenamento à 8 ºC. O produto A é uma mistura de nisina encapsulada, nisina livre e extrato de alecrim, enquanto o produto B é uma mistura de nisina livre e extrato de alecrim. L. monocytogenes foi capaz de se multiplicar em todas as formulações de mortadela ao longo do período de armazenamento. Entretanto, o produto A exerceu efeito antimicrobiano contra este patógeno. Após 10 dias de armazenamento, as contagens de L. monocytogenes nas mortadelas formuladas com o produto A foram 3 log UFC/g inferiores às contagens observadas nas demais formulações avaliadas (produto B, lactato de sódio e controle), além disso, o produto A foi capaz de reduzir a velocidade de multiplicação deste microrganismo. Em relação às salsichas tratadas com fumaça líquida, as contagens de L. monocytogenes, no oitavo dia de armazenamento foram 3 log UFC/g inferiores às contagens de L. monocytogenes nas salsichas formuladas com lactato de sódio e controle. Ao final do período de armazenamento (28 dias) observou-se diferença de 2 log UFC/g nas contagens de L. monocytogenes entre as salsichas formuladas com lactato de sódio + fumaça líquida e as demais formulações. A fumaça líquida foi capaz de inibir a multiplicação de bolores e leveduras por 21 dias de armazenamento, observando-se diferença de 2 log UFC/g entre as contagens observadas nas salsichas imersas em fumaça líquida e não imersas. As contagens de BAL permaneceram baixas ao longo do período de armazenamento (< 2 log UFC/g). Também não foi observada alteração nos valores de pH e atividade de água dos produtos cárneos, o que permite concluir que as diferenças observadas nas contagens de L. monocytogenes e bolores e leveduras são devidas à ação dos antimicrobianos adicionados aos produtos cárneos. A partir destes resultados é possível concluir que o produto A e a fumaça líquida são uma barreira adicional para o controle de L. monocytogenes em mortadela e salsichas, respectivamente, durante armazenamento a 8ºC. / Ready-to-eat meat products are among the foods most frequently associated to outbreaks of listeriosis, a disease caused by Listeria monocytogenes. The objective of the present study was to evaluate the antimicrobial activity of sodium lactate and two nisin-based commercial products (A and B) in bologna, and sodium lactate and liquid smoke in frankfurters, experimentally contaminated with a pool of six strains of L. monocytogenes, during storage at 8 ºC under vacuum. The antimicrobial with better activity against L. monocytogenes was also evaluated against yeasts and molds and lactic acid bacteria. Product A is a mixture of encapsulated nisin, free nisin and rosemary extract, and product B is a mixture of free nisin and rosemary extract. L. monocytogenes was able to grow in all bologna formulations during storage. However, product A was capable of reducing the growth rate of the microorganism. Besides, L. monocytogenes populations in bologna formulated with product A were 3 log CFU/g lower than the population observed for control samples, after 10 days of storage at 8 ºC. Regarding frankfurter samples, the use of liquid smoke alone or in combination with sodium lactate resulted in a 3 log CFU/g difference between L. monocytogenes counts found in control and treated samples, after 8 days of storage at 8 ºC. However, after 28 days only the samples treated with liquid smoke combined with sodium lactate presented lower counts than controls (2 log CFU/g). Liquid smoke was also able to inhibit the growth of yeasts and molds in frankfurters, for 21 days of storage at 8 ºC. Low counts of lactic acid bacteria (< 2 log CFU/g) were detected in frankfurters during the storage. There was no variation on pH and water activity values in the meat products during storage period; therefore, the differences found in counts of L. monocytogenes in the meat products can be attributed to the presence of the antimicrobials added in the formulations. Hence, product A and liquid smoke appear to be an additional barrier to control L. monocytogenes in bologna and frankfurters, respectively, during storage at 8 ºC.

Made available in DSpace on 2015-04-17T14:49:42Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 1556222 bytes, checksum: ff5f5ab067a6252f9aef5be2f52b8e69 (MD5) Previous issue date: 2014-03-31 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES / The Brazilian production of marine shrimp is mainly focused on the domestic market, which better absorbs the headless and peeled product, which generates significant amount of agro-industrial waste. The objective of this research was to develop biodegradable films of chitosan from the exoskeleton of marine shrimp vannamei Litopeanaeus added liquid smoke for use in sausages. For characterization of chitosan obtained from the exoskeleton of shrimp were employed methodologies for determining viscosity , conductometry , spectroscopy in the infrared and x-ray diffraction to characterize the polymer and performed tests of tensile strength , elastic modulus , solubility , opacity and thickness to characterize the films . The results were efficient for the determination of chitosan, and consistent with the literature regarding the characterization of polymeric films of origin. Microbiological analyzes were performed on the sausages before and after preparation according to ANVISA Resolution on January 12, 2001, in the chitosan films with and without plasticizer added to liquid smoke for coating sausages in order to increase the shelf life of the product the antimicrobial activity of the films was determined by the agar diffusion method on bacterial strains: Escherichia coli active, Pseudomonas aeruginosa and Staphylococcus coagulase positive. In the results , not presence of coliforms at 45 º C , coagulase Staphyilococcus positive , were observed Clostridium sulfite reducer was not detected the presence of Salmonella sp, as the antimicrobial activity , inhibition zones were found in biofilm added liquid smoke , only to Escherichia coli. As for the sensory properties of sausages packaged in three types of biodegradable chitosan film extracted from the exoskeleton of marine shrimp were differentiated by the addition of liquid smoke concentrations: 5 %, 7% and 10%. A nine-point hedonic scale was used to analyze the difference of control and acceptance testing were assessed using internal preference mapping (MEDPRF). The results indicated a significant difference between the control, conventional polyethylene film and biodegradable chitosan film plus smoke. By Preference Mapping revealed that the coated film containing sausages with liquid smoke in concentrations of 5 % and 7 %, no statistical differences obtained for the attributes: Appearance, Aroma, Taste, texture and overall acceptance levels in the addition of adding smoke compared to the control sample and 10 % ¨ smoke. It was observed in this work that the mechanical analyzes of biodegradable chitosan film is presented as a low elasticity and high tensile strength , and acceptable as opacity, solubility and thickness and that more research needs to be conducted in order to prepare chitosan films more flexible and resistant. / A produção brasileira de camarão marinho está voltada principalmente para o mercado interno, que absorve melhor o produto descabeçado e descascado, o que gera quantidade relevante de resíduos agroindustriais. O objetivo desta pesquisa foi o desenvolvimento de filmes biodegradáveis de quitosana a partir do exoesqueleto do camarão marinho Litopeanaeus vannamei adicionados de fumaça líquida, para aplicação em salsichas. Para caracterização da quitosana foram empregadas as metodologias de determinação da viscosidade, condutimetria, espectroscopia na região do infravermelho e difração de raio-x para caracterização do polímero e realizados os testes de resistência a tração, módulo elásticos, solubilidade, opacidade e espessura para caracterização dos filmes. As análises microbiológicas foram realizadas nas salsichas antes e após acondicionamento segundo a Resolução da ANVISA no 12 de janeiro de 2001, nos de filmes de quitosana com e sem plastificante adicionada de fumaça liquida, para o recobrimento de salsichas visando o aumento da vida de prateleira do produto ,a atividade antimicrobiana dos filmes foi determinada mediante teste de difusão em ágar sobre as cepas bacterianas: Escherichia coli ativa, Pseudomonas aeruginosa e Staphylococcus coagulase positiva. Nos resultados, não foram observadas presença de coliformes a 45 ºC, Staphyilococcus coagulase positiva, Clostridium sulfito redutor e não foi detectada a presença de Salmonella sp, quanto à ação antimicrobiana, foram encontrados halos de inibição no biofilme adicionado de fumaça liquida, apenas para Escherichia coli. Quanto às propriedades sensoriais de salsichas embaladas com três tipos de filme biodegradável de quitosana foram diferenciadas pela adição de fumaça liquida nas concentrações de 5%, 7% e 10%. Uma escala hedônica de nove pontos foi empregada para analise de diferença de controle e os testes de aceitação foram analisados pela metodologia de Mapa de Preferência Interno (MEDPRF). Os resultados indicaram que houve diferença significativa entre o controle, filme convencional de polietileno e os filmes biodegradável de quitosana acrescidos de fumaça líquida. Pela análise do Mapa de Preferência observou-se que as salsichas recobertas com filme contendo fumaça liquida nas concentrações de 5% e 7%, não diferenças estatísticas obteve para os atributos: Aparência, Aroma, Sabor, Textura e Aceitação global na adição teores de adição de fumaça, quando comparados com a amostra controle e 10¨% de fumaça. Foi possível observar que as análises mecânicas do filme biodegradável de quitosana apresentaram-se como de baixa elasticidade e alta resistência a tração, e aceitáveis quanto a opacidade, solubilidade e espessura e que mais pesquisas precisam ser realizadas a fim de elaborar filmes de quitosana mais flexíveis e resistentes. Concluímos que os resultados encontrados foram eficientes para determinação da quitosana, e compatíveis com a literatura quanto à caracterização de filmes de origem polimérica.

Os produtos cárneos prontos para consumo estão entre os principais alimentos associados a surtos de listeriose, uma doença causada por Listeria monocytogenes. Este estudo objetivou avaliar a ação antimicrobiana do lactato de sódio e de duas formulações comerciais à base de nisina (produtos A e B) em mortadela, e do lactato de sódio e fumaça líquida em salsicha, experimentalmente contaminadas com um pool de seis cepas de L. monocytogenes, durante o armazenamento à vácuo à 8 ºC. Os aditivos com melhor atividade anti-listeria também foram avaliados quanto ao controle de bactérias láticas (BAL) e bolores e leveduras em produto cárneo, durante o armazenamento à 8 ºC. O produto A é uma mistura de nisina encapsulada, nisina livre e extrato de alecrim, enquanto o produto B é uma mistura de nisina livre e extrato de alecrim. L. monocytogenes foi capaz de se multiplicar em todas as formulações de mortadela ao longo do período de armazenamento. Entretanto, o produto A exerceu efeito antimicrobiano contra este patógeno. Após 10 dias de armazenamento, as contagens de L. monocytogenes nas mortadelas formuladas com o produto A foram 3 log UFC/g inferiores às contagens observadas nas demais formulações avaliadas (produto B, lactato de sódio e controle), além disso, o produto A foi capaz de reduzir a velocidade de multiplicação deste microrganismo. Em relação às salsichas tratadas com fumaça líquida, as contagens de L. monocytogenes, no oitavo dia de armazenamento foram 3 log UFC/g inferiores às contagens de L. monocytogenes nas salsichas formuladas com lactato de sódio e controle. Ao final do período de armazenamento (28 dias) observou-se diferença de 2 log UFC/g nas contagens de L. monocytogenes entre as salsichas formuladas com lactato de sódio + fumaça líquida e as demais formulações. A fumaça líquida foi capaz de inibir a multiplicação de bolores e leveduras por 21 dias de armazenamento, observando-se diferença de 2 log UFC/g entre as contagens observadas nas salsichas imersas em fumaça líquida e não imersas. As contagens de BAL permaneceram baixas ao longo do período de armazenamento (< 2 log UFC/g). Também não foi observada alteração nos valores de pH e atividade de água dos produtos cárneos, o que permite concluir que as diferenças observadas nas contagens de L. monocytogenes e bolores e leveduras são devidas à ação dos antimicrobianos adicionados aos produtos cárneos. A partir destes resultados é possível concluir que o produto A e a fumaça líquida são uma barreira adicional para o controle de L. monocytogenes em mortadela e salsichas, respectivamente, durante armazenamento a 8ºC. / Ready-to-eat meat products are among the foods most frequently associated to outbreaks of listeriosis, a disease caused by Listeria monocytogenes. The objective of the present study was to evaluate the antimicrobial activity of sodium lactate and two nisin-based commercial products (A and B) in bologna, and sodium lactate and liquid smoke in frankfurters, experimentally contaminated with a pool of six strains of L. monocytogenes, during storage at 8 ºC under vacuum. The antimicrobial with better activity against L. monocytogenes was also evaluated against yeasts and molds and lactic acid bacteria. Product A is a mixture of encapsulated nisin, free nisin and rosemary extract, and product B is a mixture of free nisin and rosemary extract. L. monocytogenes was able to grow in all bologna formulations during storage. However, product A was capable of reducing the growth rate of the microorganism. Besides, L. monocytogenes populations in bologna formulated with product A were 3 log CFU/g lower than the population observed for control samples, after 10 days of storage at 8 ºC. Regarding frankfurter samples, the use of liquid smoke alone or in combination with sodium lactate resulted in a 3 log CFU/g difference between L. monocytogenes counts found in control and treated samples, after 8 days of storage at 8 ºC. However, after 28 days only the samples treated with liquid smoke combined with sodium lactate presented lower counts than controls (2 log CFU/g). Liquid smoke was also able to inhibit the growth of yeasts and molds in frankfurters, for 21 days of storage at 8 ºC. Low counts of lactic acid bacteria (< 2 log CFU/g) were detected in frankfurters during the storage. There was no variation on pH and water activity values in the meat products during storage period; therefore, the differences found in counts of L. monocytogenes in the meat products can be attributed to the presence of the antimicrobials added in the formulations. Hence, product A and liquid smoke appear to be an additional barrier to control L. monocytogenes in bologna and frankfurters, respectively, during storage at 8 ºC.

No description available.

Master of Science / Food Science Institute - Animal Science & Industry / Fadi M. Aramouni / Smoke flavored foods continue to be a popular choice among consumers. In this study, a caramel-type flavor in whipped cream applications via Maillard reaction pathways was evaluated. A highly refined liquid smoke fraction was developed using a delignified pulp wood source, and a patented activated carbon filtration process. To maximize sensory and reactionary capabilities, a liquid smoke fraction with phenol and carbonyl concentrations of 0.07mg/ml and 12.9g/100ml, respectively, was developed. Heavy cream containing a 0.075% addition of the refined liquid smoke fraction was evaluated when reacted at 50, 63, and 72°C for 15 sec prior to chilling at 0°C for 12 h, and whipping for 8 min using a handheld mixer. Sensory analysis showed the addition of liquid smoke increased whipped cream sweetness and caramel flavors, while imparting minimal off-flavors. Probable Maillard pathways were predicted for the reaction taking place between the liquid smoke and the dairy proteins upon thermal processing. This technology can be used to develop other foods which are not traditionally smoke flavored.

Catfish fillets that were enhanced with salt and various phosphate treatments through vacuum tumbling or multi-needle injection were evaluated for yield, protein exudate (only tumbling), surface color, pH, cooking loss, tenderness, purge loss and shelf-life. An agglomerated sodium phosphate blend (AGSP) was the optimum treatment for both vacuum tumbling and multi-needle injection and was further utilized in conjunction with potassium lactate (PL) and/or potassium acetate (PA) through vacuum tumbling to determine their effect on the quality, shelf-life and sensory characteristics of enhanced catfish fillets. In addition, the combination of AGSP and PA+PL that maximized shelf-life was further utilized in conjunction with liquid or wood smoking to evaluate the quality and inhibition of L. monocytogenes growth in ready-to-eat (RTE) smoked catfish fillets. All phosphate treatments increased (P<0.05) tenderness, but AGSP that contained mono-, tri-, and polyphosphates increased (P<0.05) pH and yield and decreased (P<0.05) yellowness in both tumbling and injection systems when compared to the control treatment. In addition, AGSP decreased (P<0.05) protein exudate when fillets were tumbled and increased (P<0.05) solution pick-up when injected. Psychrotrophic plate counts (PPC) for all phosphate treatments were similar to the control at each storage time and reached 7 log CFU/g by day 7 of storage; however, when AGSP was used in conjunction with PA+PL, PPC and sensory spoilage scores of raw catfish fillets were lower (P<0.05) than the control at each storage time. Marinating with a combination of 0.25% PA and 0.58% PL increased shelf-life (P<0.05) to between 10 and 14 days when compared to the control which had a shelf-life between 7 and 10 days. In addition, consumers preferred (P<0.05) fried catfish fillets that were treated with AGSP with and without PA+PL when compared to non-marinated controls with respect to appearance, flavor and overall acceptability. In conclusion, AGSP optimized yield and improved the quality of refrigerated catfish fillets, and extended shelf-life three days over other treatments when combined with PA+PL. This combined treatment also enhanced sensory properties of fried catfish fillets and had a synergistic effect with wood smoke constituents that inhibited the growth of L. monocytogenes on RTE smoked catfish fillets.

This study is based at Rocky Canyon Quarry (RCQ), a 200-acre granite aggregate open-pit quarry with chaparral-dominated plant communities located in San Luis Obispo County, CA. At RCQ, the Surface Mining and Reclamation Act (SMARA) of 1975 was interpreted as restoring the landscape to native plant communities. Native plant community restoration projects have occurred there since 1993 through cooperation with California Polytechnic State University Biology Department in San Luis Obispo, CA. I evaluated past restoration at RCQ and researched new techniques to improve chaparral restoration based on the natural processes of fire. Chaparral is an important fire-dominated plant community within the California Floristic Province, which covers about seven percent of California. Typically during a fire, heat immediately acts on Adenostoma fasciculatum (Chamise) seeds/m2 in the soil seed bank. Smoke also reaches seeds on and near the soil surface. Chemical effects of fire, such as smoke and charcoal, are deposited on the soil surface and leach into the seed bank after fall rains. In nature, this results in enhanced germination of the seeds and the beginning of chaparral post-fire succession. Fire effects, both heat and chemical, have been supported to increase seed germination in numerous laboratory and field studies. I sought to utilize natural fire cues, such as heat, charate, and liquid smoke, to develop successful and efficient restoration prescriptions. The most successful restoration technique developed utilized Wright’s Liquid Smoke and heat to increase seed germination of Adenostoma fasciculatum (Chamise), Ceanothus cuneatus (California lilac), and Salvia mellifera (Black Sage) significantly. A new restoration prescription for RCQ based on literature reviews and the above mentioned research is presented.

<p><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a>ABSTRACT</a></p> <p>Phenols are ubiquitous in our surroundings including biological molecules such as L-Dopa metabolites, food components, such as whiskey and liquid smoke, etc. This dissertation describes a new method for detecting phenols, by reaction with Gibbs reagent to form indophenols, followed by mass spectrometric detection. Unlike the standard Gibbs reaction which uses a colorimetric approach, the use of mass spectrometry allows for simultaneous detection of differently substituted phenols. The procedure is demonstrated to work for a large variety of phenols without <i>para</i>‐substitution. With <i>para</i>‐substituted phenols, Gibbs products are still often observed, but the specific product depends on the substituent. For <i>para</i> groups with high electronegativity, such as methoxy or halogens, the reaction proceeds by displacement of the substituent. For groups with lower electronegativity, such as amino or alkyl groups, Gibbs products are observed that retain the substituent, indicating that the reaction occurs at the <i>ortho</i> or <i>meta</i> position. In mixtures of phenols, the relative intensities of the Gibbs products are proportional to the relative concentrations, and concentrations as low as 1 μmol/L can be detected. The method is applied to the qualitative analysis of commercial liquid smoke, and it is found that hickory and mesquite flavors have significantly different phenolic composition.</p> <p>In the course of this study, we used this technique to quantify major phenol derivatives in commercial products such as liquid smoke (catechol, guaiacol and syringol) and whiskey (<i>o</i>-cresol, guaiacol and syringol) as the phenol derivatives are a significant part of the aroma of foodstuffs and alcoholic beverages. For instance, phenolic compounds are partly responsible for the taste, aroma and the smokiness in Liquid Smokes and Scotch whiskies. </p> <p>In the analysis of Liquid Smokes, we have carried out an analysis of phenols in commercial liquid smoke by using the reaction with Gibbs reagent followed by analysis using electrospray ionization mass spectrometry (ESI-MS). This analysis technique allows us to avoid any separation and/or solvent extraction steps before MS analysis. With this analysis, we are able to determine and compare the phenolic compositions of hickory, mesquite, pecan and apple wood flavors of liquid smoke. </p> <p>In the analysis of phenols in whiskey, we describe the detection of the Gibbs products from the phenols in four different commercial Scotch whiskies by using simple ESI-MS. In addition, by addition of an internal standard, 5,6,7,8-tetrahydro-1-napthol (THN), concentrations of the major phenols in the whiskies are readily obtained. With this analysis we are able to determine and compare the composition of phenols in them and their contribution in the taste, smokey, and aroma to the whiskies.</p> <p>Another important class of phenols are found in biological samples, such as L-Dopa and its metabolites, which are neurotransmitters and play important roles in living systems. In this work, we describe the detection of Gibbs products formed from these neurotransmitters after reaction with Gibbs reagent and analysis by using simple ESI‐MS. This technique would be an alternative method for the detection and simultaneous quantification of these neurotransmitters. </p> <p>Finally, in the course of this work, we found that the positive Gibbs tests are obtained for a wide range of <i>para</i>-substituted phenols, and that, in most cases, substitution occurs by displacement of the <i>para</i>-substituent. In addition, there is generally an additional unique second-phenol-addition product, which conveniently can be used from an analytical perspective to distinguish <i>para</i>-substituted phenols from the unsubstituted versions. In addition to using the methodology for phenol analysis, we are examining the mechanism of indophenol formation, particularly with the <i>para</i>-substituted phenols. </p> <p>The importance of peptides to the scientific world is enormous and, therefore, their structures, properties, and reactivity are exceptionally well-characterized by mass spectrometry and electrospray ionization. In the dipeptide work, we have used mass spectrometry to examine the dissociation of dipeptides of phenylalanine (Phe), containing sulfonated tag as a charge carrier (Phe*), proline (Pro) to investigate their gas phase dissociation. The presence of sulfonated tag (SO₃^-) on the Phe amino acid serves as the charge carrier such that the dipeptide backbone has a canonical structure and is not protonated. Phe-Pro dipeptide and their derivatives were synthesized and analyzed by LCQ-Deca mass spectroscopy to get the fragmentation mechanism. To confirm that fragmentation path, we also synthesized dikitopeparazines and oxazolines from all combinations of the dipeptides. All these analyses were confirmed by isotopic labeling experiments and determination and optimization of structures were carried out using theoretical calculation. We have found that the fragmentation of Phe*Pro and ProPhe* dipeptides form sequence specific b₂ ions. In addition, not only is the ‘mobile proton’ involved in the dissociation process, but also is the ‘backbone hydrogen’ is involved in forming b₂ ions. </p> <p> </p>