A crude enzyme extract (FI) of polyphenol esterase (PPE), obtained from the microbial culture of Aspergillus niger, was partially purified by ammonium sulfate precipitation. The partially purified fraction (FII) was subjected to further purification by ion-exchange chromatography, which resulted in five separated fractions, FIIIa, FIIIb, FIIIc, FIIId and FIIIe), where FIIIa showed the highest PPE activity towards chlorogenic acid, as substrate. The biocatalysis of the PPE with a wide range of mono- and diphenols, as substrates, was shown to inhibit mushroom tyrosinase (PPO) activity. Fraction FIIIa exhibited an inhibitory effect, measured spectrophotometrically, on PPO activity with the monophenols, including 4-hydroxyphenylpyruvic acid and m- and p-cresols and the diphenols, including chlorogenic acid, catechin, 3,4-dihydroxyphenylacetic acid (DHPAA), L-3,4-dihydroxyphenylalanine (L-DOPA), 4-methylcatechol, catechol and caffeic acid; however, using the polarographic method, the inhibition of PPO activity by PPE biocatalysis occurred with the diphenols but not with the monophenols. The selected enzymatic fraction FIIIa was further purified, using size-exclusion chromatography, which resulted in three fractions FIVa, FIVb and FIVc. Although fraction FIVc contained the highest PPE activity, it showed a lack of enzyme stability. Fraction FIIIa was therefore, subjected to further purification by hydrophobic interaction chromatography thereby yielding fractions FVa, FVb, FVc, FVd, FVe, FVf and FVg, where fraction FVc showed the highest PPE activity. The denatured electrophoretic analysis of fraction FVc showed the presence of one major band, with a molecular weight of 60 kDa. The successive purification of PPE resulted in a marked increase in the inactivation of PPO activity with diphenols, as demonstrated by both the lower I50 and inhibition dissociation constant (Ki) values. The purified fraction FVc was shown to exhibit, spectrophotometrically, a competitive and un

In order to establish the potential of an esterase from Lactobacillus casei for application in the dairy industry, this study was designed with the following objectives: (1) to determine the optimal cultural conditions for growth and enzyme production, (2) to construct a positive selection vector with low copy number for gene cloning, (3) to clone and sequence the gene encoding for esterase, (4) to biochemically characterize the purified recombinant esterase, and (5) to over-express an esterase of L. casei into Escherichia coli as well as into a methylotrophic yeast, Pichia pastoris using strong promoters. / Maximal growth and enzyme production in L. casei were obtained after 20 h in basal MRS medium containing 1% (w/v) lactose at pH 7.0, 30°C. Among various substrates (C2--C16) tested, the highest activity was towards C6 and C8. Although the enzyme was produced constitutively, tributyrin induced the enzyme production by a 2.5 fold. / A new E. coli and lactic acid bacteria shuttle vector with low copy and positive selection termed pCWL70 was constructed. High transformation efficiency and significant vector stability of pCWL70 were found in L. casei and Lactococcus lactis. / An esterase gene (estI) of L. casei CL96 was localized in a 3.3 kb Bam HI DNA fragment that contains an open reading frame of 1,800 bp. The open reading frame estI was isolated by PCR and subcloned into the E. coli expression vector pET29a, and Pichia expression vector pPICZ B, that allows the inducible expression under the control of the T7 promoter and an alcohol oxidase promoter (AOX1), respectively. E. coli BL21(DE3)pLysS containing estI expressed a novel 67.5 kDa protein corresponding to the EstI in N-terminal fusion with the S · tag peptide. / An esterase of L. casei CL96 was successfully over-expressed in E. coli up to 500 folds (about 25% of total cellular protein) as well as in the P. pastoris. In high cell density fed-batch fermentation, the recombinant Pichia strain containing linearized pCESTc was grown at pH 6.5 and 30°C, and the cell density peaked at about 180 h with 468 g wet cell weight per liter. The final yield was 3.7 x 106 units/ml, which is 980-folds higher than that of native L. casei cells. / The amino acid sequence of EstI indicated that the esterase is a member of a novel GHSMG family of lipolytic enzymes and S-formylglutathione hydrolases (FGH). The putative catalytic triad of EstI consists of residues Ser325, Asp516 and His558 as demonstrated by amino acid sequence alignments. (Abstract shortened by UMI.)

Made available in DSpace on 2012-09-06T01:12:45Z (GMT). No. of bitstreams: 2 license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) 982.pdf: 409747 bytes, checksum: c12619c60087f3fd431361c509f175fe (MD5) Previous issue date: 2007 / (...) O objetivo desse trabalho foi a implantação de um bioindicador para OPIDN, tendo por base a metodologia clássica para determinação de NTE em linfócitos, que possibilitasse monitorar a intoxicação humana por pesticidas com potencial para desenvolver essa síndrome. A substituição de MPX por clorpirifós-oxon (CPO) e de etPXN por metil-paraoxon (metPXN) levou a resultados muito diferentes dos obtidos com etPXN e MPX. A paralisaçãoda reação com detergente ao invés de ácido perclórico se mostrou mais eficiente, eliminando a etapa de centrifugação. Não foi possível eselecer uma técnica deconservação para as preparações de linfócitos o que obriga que a determinação seja feita no mesmo dia da coleta do sangue. Uma avaliação em um grupo de 27 voluntários sadios indicou um valor de 11,42 mais ou menos 6,33 Unidades de NTE por gramade proteínas totais (U/g Ptn), não havendo diferenças com relação ao sexo. A grande variabilidade dos valores encontrados em uma população sadia, mesmo que compatível com os resultados da literatura, dificulta a proposta de NTE linfocitária como bioindicador de OPIDN.

Made available in DSpace on 2014-06-11T19:32:14Z (GMT). No. of bitstreams: 0 Previous issue date: 2007-04-26Bitstream added on 2014-06-13T20:03:27Z : No. of bitstreams: 1 bernardo_aa_dr_sjrp.pdf: 946735 bytes, checksum: 8ca5645baf7f63ca8f1850d734030e34 (MD5) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / Os padrões de esterases de 19 linhagens de 10 espécies do grupo saltans foram analisados usando eletroforese em gel de poliacrilamida e α e β-naftil acetatos como substratos. Cinqüenta e uma bandas esterásicas foram detectadas e classificadas como 31 α-esterases, 18 β-esterases e duas α/β-esterases. Com base nos padrões de inibição usando Malathion e sulfato de eserina, 34 bandas foram classificadas como carboxilesterases, 14 como acetilesterases e três como colinesterases. Dez loci gênicos foram tentativamente estabelecidos com base nos dados de posição da banda no gel, preferência ao substrato e padrões de inibição. Vinte bandas foram espécie-específicas, as restantes foram compartilhadas por espécie de um mesmo ou diferentes subgrupos. Sete bandas α-esterásicas foram observadas exclusivamente em machos. Bandas com diferentes freqüências ou grau de expressão entre os sexos também foram detectadas. Nos géis preparados para análise da expressão dos genes nas partes do corpo (cabeça, tórax e abdome), o grau de expressão das β- esterases foi alto no tórax, enquanto as α-esterases expressaram-se predominantemente no abdome e tórax. Uma visão global dos dados, atualmente disponíveis, quanto às esterases das espécies do grupo saltans é apresentada neste trabalho. As hipóteses filogenéticas geradas à partir dos dados deste estudo foram comparadas com filogenias anteriores baseadas na morfologia, bioquímica e características moleculares. / The esterase patterns of 19 strains from 10 species in the saltans group were analyzed using polyacrylamide gel electrophoresis and α- and β-naphthyl acetates as substrates. Fifty-one esterase bands were detected and classified as 31 α-esterases, 18 β-esterases and two α/β- esterases. On the basis of the inhibition patterns using Malathion and eserine sulfate, 34 bands were classified as carboxylesterases, 14 as acethylesterases and three as cholinesterases. Ten gene loci were tentatively established on the basis of data on band position in the gel, substrate preference and inhibition pattern. Twenty bands were species-specific, the remaining being shared by species from the same or different subgroups. Seven α-esterase bands were observed exclusively in males. Bands with a different frequency or degree of expression between sexes were also detected. In the gels prepared for analysis of gene expression in the body parts (head, thorax and abdomen), the degree of expression of the β- esterases was higher in the thorax, while the α-esterases were expressed predominantly in the abdomen and thorax. A global view of the data available at present on the esterases of species from the saltans group is presented. Phylogenetic hypotheses generated from data in this study are compared with prior phylogenies based on morphological, biochemical and molecular characteristics.

Made available in DSpace on 2015-09-17T15:24:09Z (GMT). No. of bitstreams: 0 Previous issue date: 2013-12-17. Added 1 bitstream(s) on 2015-09-17T15:48:17Z : No. of bitstreams: 1 000846655.pdf: 1588788 bytes, checksum: ca68d5412270b7e10f44b091129d9d94 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / D. melanogaster e D. simulans são espécies irmãs nativas da África tropical que divergiram de um ancestral comum a cerca de dois Myr. Estas espécies têm sido comparadas em vários traços, incluindo a morfologia, fisiologia, comportamento sexual, aloenzimas e outras proteínas, inversões cromossômicas, DNA nuclear e mitocondrial, elementos transponíveis, infecção por Wolbachia entre outros. Entretanto, estudos em populações da América do Sul, inclusive do Brasil, são escassos. O objetivo principal do trabalho foi comparar linhagens geográficas de D. melanogaster e D. simulans do Brasil, África e França, quanto à suscetibilidade ao inseticida DDT, ao padrão de beta e alfa esterases, principalmente em relação à frequência do polimorfismo da esterase- 6 em indivíduos fenotipados como resistentes e suscetíveis, e a atividade da glutationa S-transferase. Ambas as espécies mostraram uma ampla variabilidade nos valores da CL50 obtidos. Os maiores valores foram observados nas linhagens africanas de D. melanogaster e D. simulans, TANA (447,89 μg/mL), e TANA-4 (920 μg/mL). A linhagem Canton-S de D. melanogaster foi a que apresentou o menor valor de CL50 = 2,99 μg/mL. Comparando as populações de mesma localidade de ambas as espécies verifica-se que as linhagens de D. melanogaster mostraram valores de CL50 maiores que os de D. simulans, com exceção da linhagem FLO onde D. simulans apresentou um valor de CL50 (94,60) ligeiramente superior ao de D. melanogaster (81,82). Foram analisadas duas bandas α-esterásicas, denominadas de α-1 e α-2, sendo que a banda α-2 foi observada em 100% de todos os indivíduos analisados de ambas as espécies. Os dados mostram maior variabilidade genética para D. melanogaster em relação à resistência ao DDT, alta resistência para as linhagens africanas de ambas as espécies, indicando que estas populações continuam sendo selecionadas por este... / D. melanogaster and D. simulans are sister species native to tropical Africa which diverged from a common ancestor about two Myr. These species have been compared in several traits, including morphology, physiology, sexual behavior, allozymes and other proteins, chromosomal inversions, nuclear and mitochondrial DNA, transposable elements, Wolbachia infection among others. However, studies in populations of South America, including Brazil, are scarce. The main objective of the study was to compare geographic strains of D. melanogaster and D. simulans from Brazil, Africa and France, for susceptibility to the insecticide DDT, the pattern of α and β esterases, especially in relation to the frequency of the polymorphism of esterase-6 in individuals phenotyped as resistant and susceptible, and the activity of glutathione-S-transferase . Both species showed a wide variability in LC50 values obtained. The highest values were observed in African strains of D. melanogaster and D. simulans, TANA (447.89 mg / mL), and TANA-4 (920 / mL). The Canton-S strain of D. melanogaster was the one with the lowest LC50 = 2.99 mg / mL. Comparing populations from the same location of both species the strains of D. melanogaster showed LC50 values larger than D. simulans, except FLO D. simulans strain had a LC50 (94.60) slightly higher than D. melanogaster (81.82). We analyzed two bands α-esterases, which we call α-1 and α-2, and the band α-2 was observed in 100% of all individuals analyzed in both species. The data show greater genetic variability for D. melanogaster for resistance to DDT, high resistance to African strains of both species, indicating that these populations continue to be selected by this or another insecticide, the lack of a cline for the F and S alleles in strains of both species, suggest that treatment with DDT may have selected individuals heterozygous for some strains, which may have masked the...

Orientador: Anita Jocelyne Marsaioli / Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica / Made available in DSpace on 2018-08-10T04:53:28Z (GMT). No. of bitstreams: 1 Mantovani_SimoneMoraes_M.pdf: 1495773 bytes, checksum: 493a0576675a8aad3c2879147aa7745f (MD5) Previous issue date: 2007 / Resumo: Nas últimas décadas as reações utilizando biocatalisadores tem sido amplamante aplicadas na síntese orgânica, como componentes chave de muitos processos químicos industriais, levando ao aumento na demanda por novas enzimas. A maneira mais rápida e simples de detectar enzimas é através de metodologias de triagem de alto desempenho (HTS) que permitam identificação rápida da atividade enzimática, como por exemplo, os ensaios utilizando compostos fluorogênicos e cromogênicos. Nesse trabalho nós aplicamos HTS baseado em substratos fluorogênicos para detecção de epóxido-hidrolases e esterases em microrganismos brasileiros. Inicialmente foram selecionados cinco microrganismos com alta atividade epóxido-hidrolase, e 18 pela a presença de esterases. Inspirados nesse principio nós adaptamos a metodolgia conhecida como "Quick E" para a avaliação rápida das enantiosseletividades de epóxido-hidrolases em células íntegras através de medidas das velocidades iniciais de substratos fluorogênicos quirais avaliados separadamente com adição de um competidor. Os ensaios de enantiosseletividade mostraram que os experimentos com competidor apresentaram valores de enatiosseletividade muito próximos dos valores de E determinados via biocatálise convencional. Além disso, alguns microrganismos selecionados por HTS foram testados para reações de biotransformação frente a substratos de interesse sintético, o que permitiu, além da confirmação das atividades enzimáticas e seletividades observadas, detectar a capacidade do microrganismo C. albícans CCT 0776 de desracemizar álcoois secundários por estereoinversão, fornecendo o (S)-1,2-octanodiol com 100 % de rendimento teórico e ee > 99 %, e o (S)-4-fenilmetoxi-1,2-butanodiol com ee 45 % / Abstract: Since the past decades the biocatalysts have been applied in organic chemistry, as key components of many industrial chemical processes, thus increasing the demand for novel enzymes. High-Throughput Screening (HTS), using fluorogenic probes are among the best assays to discovery new enzymes, easily adapted to whole cells format. In this work, have been applied fluorogenic probes to screen epoxide hydrolases and esterases in Brazilian Collection Cultures of microorganisms, which allowed to detect epoxide hydrolases in five microorganisms, and esterases in 18 microrganisms. Additionally, were used chiral probes to implement a Quick E assay, for a fast valuation of epoxide hydrolases enantioselectivity by measuring initial rates of pure enantiomers. Optimization of the methodology revealed that almost true E were obtained by competitive experiments of each enantiomer and a substrate of similar reactivity. The quick E assay was validated by determining conversion and ee using GC/MS and NMR (using mandelic acid derivatives) and is now a new method to determine the enantiomeric ratio for epoxide hidrolases. Finally, the outstanding HTS results were better investigated by conventional catalysis detecting a stereoinversion process performed by C. albicans CCT 0776, which furnished (S)-1 ,2-octanodiol in 100 % theoretical yield and ee of 100%, and (S)-4-fenilmetoxi-1,2-butanodiol in ee of 45% / Mestrado / Quimica Organica / Mestre em Química

Over the past few years, the use of enzymes as catalysts for the preparation of novel organic molecules has received a steadily increasing amount of attention. Lipolytic enzymes are widely distributed in nature and attract great attention because of their biotechnological potential, as they catalyse the enantio- and regioselective hydrolysis and synthesis of a broad range of natural and non-natural esters. Bacteria produce different lipolytic enzymes, such as esterases (EC 3.1.1.1), which hydrolyse ester-containing molecules at least partly soluble in water, and lipases (EC 3.1.1.3), which hydrolyse water-insoluble long-chain triglycerides. In this study, a bacterial isolate, B. coagulans strain 81-11, isolated from popcorn seeds, was characterized with the specific aim of isolating and characterizing genes encoding novel lipolytic enzymes. A genomic library of B. coagulans strain 81-11 was screened in Escherichia coli JM83 for lipolytic activity by using tributyrin agar plates. A 2.4-kb DNA fragment was subcloned from a lipolytic-positive clone and completely sequenced. Nucleotide sequence analysis predicted a 723-bp open reading frame (ORF), designated estCl, encoding a protein of 240 amino acids with an estimated molecular mass of 27 528 Da and a pI of 9.15. The deduced amino acid sequence of the estCl gene exhibited significant amino acid sequence identity with carboxyl esterases and sequence analysis showed that the protein contains the signature G-X-S-X-G included in most esterases and lipases. Enzyme assays using p-nitrophenyl esters with different acyl chain lengths as the substrate confirmed the anticipated esterase activity. EstCl exhibited a marked preference for esters of short-chain fatty acids, yielding the highest activity with p-NP butyrate. Maximum activity was found at pH 8 and 50°C, although the enzyme was active in the pH range 7-9 and displayed activity at temperatures up to 55°C. Since bacterial esterases are potentially important for a variety of biotechnological applications, there is a considerable industrial interest to produce these enzymes at a larger scale. Among the many systems that are available for heterologous protein production, attempts were made to over express the newly identified B. coagulans estCI esterase¬encoding gene in different Gram-positive bacteria, as they are well known for their important contribution to food biotechnology and as production organisms for industrial enzymes. A recombinant expression vector was thus constructed (pMG36-EstCl) and introduced in Lactococcus lactis, Lactobacillus plantarum and Bacillus subtilis strains 154 and lA297. Of these different bacterial hosts, high levels of intracellular esterase activity were detected in B. subtilis lA297 only. In an attempt to increase extracellular expression of the B. coagulans EstCl esterase, a recombinant secretion plasmid (pNW-EstClaps) was constructed that contained an alkaline protease promoter and signal sequence from a Bacillus species. Following introduction of the construct in B. subtilis lA297, the derived recombinant strain displayed 2.3-fold higher extracellular esterase-activity levels than the parent B. coagulans strain, and the extracellular esterase activity represented 82% of the total esterase activity. / Dissertation (MSc (Microbiology))--University of Pretoria, 2006. / Microbiology and Plant Pathology / unrestricted

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