Abstract Lipases are hydrolases used in various sectors such as the food, pharmaceutical and chemical synthesis industries. In this study, epiphytic microorganisms were isolated from the Serra of Ouro Branco State Park (Minas Gerais, Brazil) and were subsequently evaluated for their ability to produce extracellular lipases. Among the 46 isolated strains, 25 presented positive results for lipase production in the agar plate screening assay. Two of these strains that expressed the highest diffusion halos, were genetically identified as Serratia marcescens and Pseudomonas fluorescens and catalogued in the Tropical Cultures Collection from the André Tosello Foundation/Brazil as CCT 7796 and CCT 7797, respectively. The fermentation growth kinetics indicated that the maximum extracellular lipase activities were achieved between 96 and 120h of cultivation. The highest lipolytic activity for both strains was observed at an optimum temperature and pH of 37°C and 7.0, respectively. At these conditions, the lipase activity detected in the crude enzymatic extract of both strains was close to 15.0 U/mL. We consider that these species are promising lipase producers for industrial applications.

ABSTRACT The present study aimed to compare two MALDI-TOF identification methods [(a) direct sample identification after pre-incubation; or (b) use of bacteria isolated on pre-culture)] to standard, traditional bench microbiology. A total of 120 quarter milk samples from 40 Holstein lactating cows were screened based on culture-positive results obtained by microbiological culture (reference method) with the following numbers of quarters positive per cow: 4 cows with 1, 8 cows with 2, 12 cows with 3 and 16 cows with 4 infected quarters per cow. For direct identification method, quarter milk samples (n = 120) were skimmed by centrifugation (10,000 × g/10 min) and pre-incubated at 37 ºC for 12 h. After pre-incubation, quarter milk samples were submitted to total bacterial count by flow cytometry and for a preparation protocol for bacterial ribosomal protein extraction followed by MALDI-TOF MS analysis. The direct MALDI-TOF MS identification method compared to microbiological culture correctly identified isolates of coagulase-negative Staphylococci (27.2%), Streptococcus agalactiae (21.8%), Staphylococcus aureus (14.2%), and Streptococcus uberis (5.2%). The pre-incubation protocol of milk samples, associated to the direct identification method by MALDI-TOF MS, did not increase the identification at species level (score >2.0) of pathogens causing subclinical mastitis in comparison to the method without previous incubation.

RESUMO: A espectrometria de massas (MALDI-TOF MS) tem mostrado ser um método alternativo para a identificação de bactérias, sendo capaz de identificar as bactérias causadoras de mastite em gênero, espécie ou até mesmo subespécie. Com o objetivo de identificar os patógenos causadores de mastite em grande-escala por esta plataforma, um total de 305 isolados bacterianos oriundos de vacas com mastite subclínica foram analisados pela cultura microbiológica convencional (CM) e pela MALDI-TOF MS acoplada ao software Biotyper. Aproximadamente 89% das identificações realizadas pela MALDI-TOF MS foram consistentes com os resultados obtidos pela CM. Do restante de isolados bacterianos (11%), 6,3% foram classificados como identificação errônea (discordância de gênero e espécie), e 4,7% apresentaram concordância de gênero, mas discordância da espécie. Os resultados que apresentaram divergência estavam mais associados com a identificação das espécies de Streptococcus spp. e Enterococcus spp. devido à similaridade fenotípica entre os dois gêneros. Estes resultados divergentes sugerem que os ensaios bioquímicos podem ser propensos a erros de identificação, por isso a MALDI-TOF MS pode ser considerada um método alternativo para superar os erros de identificação da CM. A cultura microbiológica padrão e os ensaios bioquímicos utilizados na identificação de agentes causadores de mastite são demorados, trabalhosos e propensos a erros quando utilizados na identificação em nível de espécie. No presente estudo, demonstramos que a MALDI-TOF MS acoplada ao software Biotyper pode ser considerada um método alternativo de identificação de bactérias causadoras de mastite em grande-escala quando comparado com a cultura microbiológica convencional.

ABSTRACT: Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) has been shown to be an alternative method for identification of bacteria via their protein profile spectra, being able to identify bacteria at the genus, species and even at subspecies level. With the aim of large-scale identification of pathogens causing mastitis by this platform, a total of 305 isolates of bacteria identified from cows with subclinical mastitis were analyzed by conventional microbiological culture (MC) as well as by MALDI-TOF MS coupled with Biotyper data processing. Approximately 89% of the identifications performed by MALDI-TOF MS were consistent with results obtained by MC. From the remaining isolates (11%), 6.3% of isolates were classified as misidentified (discordance for both genus and species level), and 4.7% showed identification agreement at the genus level but not at the species level, being classified as unidentified at species level. The disagreement results were mostly associated with identification of Streptococcus and Enterococcus species probably due to the narrow phenotypic similarity between these two genera. These disagreement results suggest that biochemical assays might be prone to identification errors and, MALDI-TOF MS therefore may be an alternative to overcome incorrect species-specific identification. Standard microbiological methods for bovine mastitis diagnosis are time consuming, laborious and prone to errors for some bacteria genera. In our study, we showed that MALDI-TOF MS coupled with Biotyper may be an alternative method for large-scale identification of bacteria isolated from milk samples compared to classical microbiological routine protocols.

ABSTRACT Jatropha is a potential oilseed crop, which requires mitigating factors such as the low genetic variability of the species. The solution runs through the research of Brazilian germplasm. Attention should be given to the germplasm of jatropha the north of Minas Gerais, because this is the oldest national collection and because this region may be a regions of jatropha diversity due to selection pressure arising from environmental adversities. Therefore, the objective of this study was to investigate the genetic diversity of 48 accessions of collection from Empresa de Pesquisa Agropecuária de Minas Gerais (EPAMIG), using SSR and ISSR markers. The results showed low genetic diversity, but some individuals stood out as J. mollissima (48), J. podagrica (47), Mexican accessions (42, 43, 44 and 45) and some national accessions (28, 29, 41 and 46). Therefore, aiming to increase the genetic variability and improve the effectiveness of jatropha breeding programs, it is suggested to explore such as parental accessions to generate commercial hybrids. This fact implies the possibility to support future production of jatropha, since this culture may be an important source of income, especially for small farmers living in semiarid regions of Brazil.

O preparo mecânico do solo é uma das práticas agrícolas que contribuem para o aumento da perda de carbono via emissão de CO2 do solo (FCO2). Com este trabalho objetivou-se investigar o efeito de três sistemas de preparo do solo na FCO2, temperatura e umidade do solo em área de reforma da cultura de cana-de-açúcar. A área experimental foi constituída de três parcelas, cada uma recebendo um dos preparos do solo: preparo convencional (PC), subsolagem convencional (SC) e subsolagem localizada (SL). A FCO2, temperatura e a umidade do solo foram avaliadas durante o período total de 17 dias. A FCO2 foi maior no preparo PC (0,75 g CO2 m-2 h-1). A temperatura do solo não diferiu (p > 0,05) entre as subsolagens: SL (26,2 ºC) e SC (25,9 ºC). A umidade do solo foi maior na SL (24%), seguida pela SC (21,8%) e preparo PC (18,3%). Apenas no preparo PC foi observada correlação significativa (r = –0,71; p < 0,05) entre FCO2 e a temperatura do solo. O preparo PC apresentou emissão total (2.864,3 kg CO2 ha-1), superior às emissões nas subsolagens: SC (1.970,9 kg CO2 ha-1) e SL (1.707,7 kg CO2 ha-1). A conversão do sistema de preparo PC para a SL diminuiu as emissões de CO2 do solo, reduzindo a contribuição da agricultura para o aumento dos gases de efeito estufa na atmosfera.

Soil tillage is one of the agricultural practices that may contribute to increase the loss of carbon through emission of CO2 (FCO2). The aim of this study was to investigate the effect of three soil tillage systems on FCO2, soil temperature and soil moisture in a sugarcane area under reform. The experimental area consisted of three tillage plots: conventional tillage (CT), conventional subsoiling (CS), and localized subsoiling (LS). FCO2, soil temperature and soil moisture were measured over a period of 17 days. FCO2 showed the highest value in CT (0.75 g CO2 m-2 h-1). Soil temperature presented no significant difference (p > 0.05) between LS (26.2 °C) and CS (25.9 °C). Soil moisture was higher in LS (24%), followed by CS (21.8%) and CT (18.3%). A significant correlation (r= ‒0.71; p < 0.05) between FCO2 and soil temperature was observed only in CT. The conventional tillage presented a total emission (2,864.3 kg CO2 ha-1) higher than the emissions observed in CS (1,970.9 kg CO2 ha-1) and LS (1,707.7 kg CO2 ha-1). The conversion from CT to LS decreased soil CO2 emissions, reducing the contribution of agriculture in increasing the concentration of greenhouse gases in the atmosphere.

Objetivou-se com este estudo avaliar os fatores de risco associados às práticas de manejo e tratamento de mastite e a resistência aos antimicrobianos de Staphylococcus aureus isolados de vacas com mastite. Foram selecionados para o presente estudo 13 rebanhos localizados na região de Pirassununga/SP. Foi aplicado um questionário contendo informações para o levantamento de fatores de risco relacionados à resistência aos antimicrobianos e às práticas de manejo e tratamento de mastite. Após a seleção dos rebanhos e aplicação dos questionários, foram utilizados 210 isolados de S. aureus de amostras compostas de leite coletadas durante 24 meses, em quatro períodos, para realização dos testes de resistência. Os antimicrobianos testados foram: ampicilina 10µg, clindamicina 2µg, penicilina 1µg, eftiofour 30µg, gentamicina 10µg, sulfatrimetropin 25µg, enrofloxacina 5µg, sulfonamida 300µg, tetraciclina 30µg, oxacilina 1µg, cefalotina 30µg e eritromicina 5µg. As variáveis que foram significativamente associadas à resistência de S. aureus foram: o tratamento da mastite clínica para ampicilina (OR = 2,18), o tratamento da vaca seca para enrofloxacina (OR=2,11), e o não envio de amostras de leite para a cultura microbiológica e testes de sensibilidade, para ampicilina (OR=2,57) e penicilina (OR=4,69). Em conclusão, a identificação dos fatores de risco para a resistência S. aureus frente aos principais agentes antimicrobianos, utilizados para tratamento da mastite, pode auxiliar o estabelecimento do uso prudente de antimicrobianos na produção de leite.

The objective of this study was to evaluate herd management practices and mastitis treatment procedures as risk factors associated with Staphylococcus aureus antimicrobial resistance. For this study, 13 herds were selected to participate in the study to evaluate the association between their management practices and mastitis treatment procedures and in vitro antimicrobial susceptibility. A total of 1069 composite milk samples were collected aseptically from the selected cows in four different periods over two years. The samples were used for microbiological culturing of S. aureus isolates and evaluation of their antimicrobial susceptibility. A total of 756 samples (70.7%) were culture-positive, and S. aureus comprised 27.77% (n=210) of the isolates. The S. aureus isolates were tested using the disk-diffusion susceptibility assay with the following antimicrobials: ampicillin 10mg; clindamycin 2μg; penicillin 1mg; ceftiofur 30μg; gentamicin 10mg; sulfa-trimethoprim 25μg; enrofloxacin 5μg; sulfonamide 300μg; tetracycline 30μg; oxacillin 1mg; cephalothin 30μg and erythromycin 5μg. The variables that were significantly associated with S. aureus resistance were as follows: the treatment of clinical mastitis for ampicillin (OR=2.18), dry cow treatment for enrofloxacin (OR=2.11) and not sending milk samples for microbiological culture and susceptibility tests, for ampicillin (OR=2.57) and penicillin (OR=4.69). In conclusion, the identification of risk factors for S. aureus resistance against various mastitis antimicrobials is an important information that may help in practical recommendations for prudent use of antimicrobial in milk production.

FUNDAMENTO: Embora se reconheça que a cirurgia de reconstrução ventricular (CRV) promova remodelamento reverso, são necessários novos estudos para definir a influência da área de fibrose do ventrículo esquerdo (VE). OBJETIVO: Avaliar se a extensão da área de fibrose do VE é importante na recuperação funcional ventricular após CRV e correlacionar com fatores clínicos. MÉTODO: Análise prospectiva de 82 pacientes com disfunção ventricular submetidos à CRV. Analisou-se a importância das características clínicas e foram avaliadas as quantidades de fibrose, mensuradas por ressonância magnética em pequena, média e grande. RESULTADOS: Todos os pacientes foram acompanhados por 36 meses, com mortalidade de 6%. A quantidade de fibrose média foi de 25,8% ± 13,6%. Houve melhora da fração de ejeção do VE (FEVE), de 36,9% ± 6,8% para 48,2% ± 8,2% (p < 0,001). Houve relação inversa entre a quantidade de fibrose o incremento da FEVE (r = -0,83, p < 0,0001). Houve diminuição do volume sistólico final do VE de 43,3 ± 8,2ml/m² (p < 0,001). Houve melhora dos sintomas de insuficiência cardíaca, exceto nos pacientes com grande área de fibrose (p = 0,45). Os preditores independentes para eventos foram: área fibrótica (p = 0,01), idade (p = 0,01), volume sistólico final do VE (p = 0,03) e fração de ejeção (p = 0,02). O seguimento livre de evento foi diferente em relação à área de fibrose (p < 0,01). CONCLUSÃO: Em pacientes com disfunção ventricular, a extensão da área fibrótica foi um preditor independente da recuperação funcional do VE após CRV. A combinação de RMC e parâmetros clínicos podem auxiliar na indicação para CRV.

BACKGROUND: Although it is acknowledged that the ventricular reconstruction surgery (VRS) can promote reverse remodeling, new studies are necessary to define the influence of the left ventricular (LV) area of fibrosis. OBJECTIVE: To evaluate whether the extension of the area of fibrosis of the LV is important in the LV functional recovery after the surgery and correlate it with clinical factors. METHODS: Prospective analysis of 82 patients with ventricular dysfunction submitted to VRS. We analyzed the importance of the clinical characteristics and the amount of fibrosis was assessed, measured by cardiac magnetic resonance (CMR) as small, medium and large. RESULTS: All patients were followed for 36 months, with a mortality of 6%. The amount of medium fibrosis was 25.8% ± 13.6%. There was improvement in the left ventricular ejection fraction (LVEF), from 36.9% ± 6.8% to 48.2% ± 8.2% (p < 0.001). There was an inverse association between the amount of fibrosis and the increase in LVEF (r = -0.83, p < 0.0001). There was a decrease in the LV end-systolic volume of 43.3 ± 8.2ml/m² (p < 0.001). There was an improvement in heart failure symptoms, except in patients with large areas of fibrosis (p = 0.45). The independent predictors for events were: fibrotic area (p = 0.01), age (p = 0.01), LV end-systolic volume (p = 0.03) and LVEF (p = 0.02). The event-free follow-up was different in relation to the area of fibrosis (p < 0.01). CONCLUSION: In patients with ventricular dysfunction, the extension of the area of fibrosis was an independent predictor of the LV functional recovery after the VRS. The combination of cardiac MRI and clinical parameters can help in the indication for VRS.

FUNDAMENTO: Si bien se reconoce que la cirugía de reconstrucción ventricular (CRV) promueve remodelación reversa, son necesarios nuevos estudios para definir la influencia del área de fibrosis del ventrículo izquierdo (VE). OBJETIVO: Evaluar si la extensión del área de fibrosis del VI es importante en la recuperación funcional ventricular tras la CRV y correlacionarlo con factores clínicos. MÉTODO: Análisis prospectivo de 82 pacientes con disfunción ventricular sometidos a CRV. Se analizó la importancia de las características clínicas y se evaluaron las áreas de fibrosis, medidas por resonancia magnética y ponderadas como pequeña, mediana y grande. RESULTADOS: Se realizó un seguimiento de 36 meses a todos los pacientes, con mortalidad del 6%. La cantidad de fibrosis promedio fue del 25,8% ± 13,6%. Existió una mejora de la fracción de eyección del VI (FEVI), del 36,9% ± 6,8% al 48,2% ± 8,2% (p < 0,001). Existió relación inversa entre la cantidad de fibrosis y el incremento de la FEVI (r = -0,83, p < 0,0001). Hubo una disminución del volumen de fin de sístole del VI de 43,3 ± 8,2ml/m² (p < 0,001). Se produjo una mejoría en los síntomas de insuficiencia cardiaca, excepto en los pacientes con gran área de fibrosis (p = 0,45). Los predictores independientes para eventos fueron: área de fibrosis (p = 0,01), edad (p = 0,01), volumen de fin de sístole del VI (p = 0,03) y fracción de eyección (p = 0,02). El seguimiento libre de eventos fue diferente en relación con el área de fibrosis (p < 0,01). CONCLUSIÓN: En pacientes con disfunción ventricular, la extensión del área de fibrosis fue un predictor independiente de la recuperación funcional del VI luego de la CRV. La combinación de RMC y parámetros clínicos puede auxiliar en la indicación de CRV.

A reprodução e a sobrevivência de Synthesiomyia nudiseta (Wulp, 1883) foram estudadas entre 22 e 28ºC, UR de 70% e fotoperíodo de 12h. Os dados foram analisados através de classes de idade, tabelas de vida de fecundidade, análise de sobrevivência pela distribuição de Weibull e análise das curvas de sobrevivência através do conceito de entropia (H). A taxa intrínseca de aumento natural (r m), taxa finita de aumento (lambda), taxa de reprodução líquida (R0) e tempo médio de uma geração (T) foram 0,534; 1,7; 59,439 e 7,65 respectivamente, sugerindo rápido crescimento populacional nestas condições. Isso foi causado pela alta fecundidade, confirmando o que ocorre para esta espécie, com média de 266 ovos/fêmea e período de pré-oviposição de 10,25 dias. O modelo de Weibull demonstrou que a sobrevivência não foi constante ao longo da vida de adultos, com mortalidade pronunciada depois da quarta e quinta semanas e valores de H intermediários aos valores teóricos esperados (0,0-0,5) para os ambos sexos, demonstrando que a curva de sobrevivência é retangular (com maior impacto da mortalidade na quarta e quinta semanas após a emergência). Os resultados apresentados podem ser considerados como base para estudos pormenorizados da dinâmica e do crescimento populacional desta espécie em hábitats naturais.

The reproduction and survival of Synthesiomyia nudiseta (Wulp, 1883) were studied between 22 and 28ºC, 70% R.H. and 12h photoperiod. The raw data were analyzed based on age-class, sex life table, Weibull distribution and entropy curve (H). The intrinsic rate of increase (r m), finite rate of increase (lambda), net reproduction rate (R0) and mean generation time (T) were 0.534, 1.7, 59.439 and 7.65 respectively, suggesting fast population growth in these conditions. That is caused by the high fecundity that was confirmed for this species with mean number of eggs/female of 266 and mean preoviposition period of 10.25 days. The Weibull survival model showed that the survival was not constant throughout the adults life: the mortality rate was more pronounced after the fourth and fifth week because both sexes had H values intermediate to those theoretically expected (0.0-0.5), showing that the survival curve is rectangular (with more impact of mortality on the fourth and fifth week from pupal emergence). The presented results can be considered as base for detailed studies on dynamics and population growth of this species in natural habitats.

A continuous assay using internally quenched fluorescent peptides with the general sequence Abz-peptidyl-(Dnp)P-OH (Abz = ortho-aminobenzoic acid; Dnp = 2,4-dinitrophenyl) was optimized for the measurement of angiotensin I-converting enzyme (ACE) in human plasma and rat tissues. Abz-FRK(Dnp)P-OH, which was cleaved at the Arg-Lys bond by ACE, was used for the enzyme evaluation in human plasma. Enzymatic activity was monitored by continuous recording of the fluorescence (lambdaex = 320 nm and lambdaem = 420 nm) at 37ºC, in 0.1 M Tris-HCl buffer, pH 7.0, with 50 mM NaCl and 10 µM ZnCl2. The assays can be performed directly in the cuvette of the fluorimeter and the hydrolysis followed for 5 to 10 min. ACE measurements in the plasma of 80 healthy patients with Hip-His-Leu and with Abz-FRK(Dnp)P-OH correlated closely (r = 0.90, P < 0.001). The specificity of the assay was demonstrated by the complete inhibition of hydrolysis by 0.5 µM lisinopril or captopril. Abz-FRK(Dnp)P-OH cleavage by ACE was monitored in rat lung, kidney, heart, and liver homogenates in the presence of a cocktail of inhibitors containing trans-epoxy-succinyl-L-leucylamido-(4-guanido)-butene, pepstatin, phenyl-methylsulfonyl fluoride, N-tosyl-L-phenylalanyl-chloromethyl ketone, and N-tosyl-lysyl-chloromethyl ketone to prevent undesirable hydrolysis. ACE activity in lung, heart and kidney homogenates, but not in liver homogenates, was completely abolished by 0.5 µM lisinopril or captopril. The advantages of the method are the procedural simplicity and the high sensitivity providing a rapid assay for ACE determinations.

The opportunistic bacterium Proteus mirabilis secretes a metalloprotease, ZapA, considered to be one of its virulence factors due to its IgA-degrading activity. However, the substrate specificity of this enzyme has not yet been fully characterized. In the present study we used fluorescent peptides derived from bioactive peptides and the oxidized ß-chain of insulin to determine the enzyme specificity. The bradykinin- and dynorphin-derived peptides were cleaved at the single bonds Phe-Ser and Phe-Leu, with catalytic efficiencies of 291 and 13 mM/s, respectively. Besides confirming already published cleavage sites, a novel cleavage site was determined for the ß-chain of insulin (Val-Asn). Both the natural and the recombinant enzyme displayed the same broad specificity, demonstrated by the presence of hydrophobic, hydrophilic, charged and uncharged amino acid residues at the scissile bonds. Native IgA, however, was resistant to hydrolysis by ZapA.

This article reviews recent results of studies aiming to elucidate modes of integrating signals initiated in ACTH receptors and FGF2 receptors, within the network system of signal transduction found in Y1 adrenocortical cells. These modes of signal integration should be central to the mechanisms underlying the regulation of the G0->G1->S transition in the adrenal cell cycle. FGF2 elicits a strong mitogenic response in G0/G1-arrested Y1 adrenocortical cells, that includes a) rapid and transient activation of extracellular signal-regulated kinases-mitogen-activated protein kinases (ERK-MAPK) (2 to 10 min), b) transcription activation of c-fos, c-jun and c-myc genes (10 to 30 min), c) induction of c-Fos and c-Myc proteins by 1 h and cyclin D1 protein by 5 h, and d) onset of DNA synthesis stimulation within 8 h. ACTH, itself a weak mitogen, interacts with FGF2 in a complex manner, blocking the FGF2 mitogenic response during the early and middle G1 phase, keeping ERK-MAPK activation and c-Fos and cyclin D1 induction at maximal levels, but post-transcriptionally inhibiting c-Myc expression. c-Fos and c-Jun proteins are mediators in both the strong and the weak mitogenic responses respectively triggered by FGF2 and ACTH. Induction of c-Fos and stimulation of DNA synthesis by ACTH are independent of PKA and are inhibited by the PKC inhibitor GF109203X. In addition, ACTH is a poor activator of ERK-MAPK, but c-Fos induction and DNA synthesis stimulation by ACTH are strongly inhibited by the inhibitor of MEK1 PD98059.

The protease ZapA, secreted by Proteus mirabilis, has been considered to be a virulence factor of this opportunistic bacterium. The control of its expression requires the use of an appropriate methodology, which until now has not been developed. The present study focused on the replacement of azocasein with fluorogenic substrates, and on the definition of enzyme specificity. Eight fluorogenic substrates were tested, and the peptide Abz-Ala-Phe-Arg-Ser-Ala-Ala-Gln-EDDnp was found to be the most convenient for use as an operational substrate for ZapA. A single peptide bond (Arg-Ser) was cleaved with a Km of 4.6 µM, a k cat of 1.73 s-1, and a catalytic efficiency of 376 (mM s)-1. Another good substrate for ZapA was peptide 6 (Abz-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-Gln-EDDnp) which was cleaved at a single bond (Phe-Ser) with a Km of 13.6 µM, a k cat of 3.96 s-1 and a catalytic efficiency of 291 (mM s)-1. The properties of the amino acids flanking the scissile bonds were also evaluated, and no clear requirement for the amino acid residue at P1 was found, although the enzyme seems to have a preference for a hydrophobic residue at P2.

We have characterized, in the Paracoccidioides brasiliensis yeast phase, an exocellular SH-dependent serine proteinase activity against Abz-MKRLTL-EDDnp and analogous fluorescent-quenched peptides, and showed that it is also active against constituents of the basement membrane in vitro. In the present study, we separated the components of P. brasiliensis culture filtrates by electrophoresis and demonstrated that the serine-thiol exocellular proteinase has a diffuse and heterogeneous migration by SDS-PAGE, localizing in a region between 69 and 43 kDa. The hydrolytic activity was demonstrable after SDS-PAGE using buffered agarose overlays of Abz-MKALTLQ-EDDnp, following incubation at 37oC, and detection of fluorescent bands with a UV transilluminator. Hydrolysis was more intense when incubation was carried out at basic pH, and was completely inhibited with 2.5 mM PMSF and partially with sodium 7-hydroxymercuribenzoate (2.5 mM p-HMB), suggesting its serine-thiol nature. A proteolytic band with similar characteristics was observed in conventional gelatin zymograms, but could not be correlated with a silver-stained component. Detection of the serine-thiol proteinase in substrate gels after SDS-PAGE provides a useful way of monitoring purification of the basement membrane degrading enzyme.

A new metalloendopeptidase was purified to apparent homogeneity from a homogenate of normal human liver using successive steps of chromatography on DEAE-cellulose, hydroxyapatite and Sephacryl S-200. The purified enzyme hydrolyzed the Pro7-Phe8 bond of bradykinin and the Ser25-Tyr26 bond of atrial natriuretic peptide. No cleavage was produced in other peptide hormones such as vasopressin, oxytocin or Met- and Leu-enkephalin. This enzyme activity was inhibited by 1 mM divalent cation chelators such as EDTA, EGTA and o-phenanthroline and was insensitive to 1 µM phosphoramidon and captopril, specific inhibitors of neutral endopeptidase (EC 3.4.24.11) and angiotensin-converting enzyme (EC 3.4.15.1), respectively. With Mr 85 kDa, the enzyme exhibits optimal activity at pH 7.5. The high affinity of this endopeptidase for bradykinin (Km = 10 µM) and for atrial natriuretic peptide (Km = 5 µM) suggests that it may play a physiological role in the inactivation of these circulating hypotensive peptide hormones.

Two intramolecularly quenched fluorogenic peptides containing o-aminobenzoyl (Abz) and ethylenediamine 2,4-dinitrophenyl (EDDnp) groups at amino- and carboxyl-terminal amino acid residues, Abz-<!-- $MVD$:face("Times") -->DArg-Arg-Leu-EDDnp (Abz-<!-- $MVD$:face("Times") -->DRRL-EDDnp) and Abz-<!-- $MVD$:face("Times") -->DArg-Arg-Phe-EDDnp (Abz-<!-- $MVD$:face("Times") -->DRRF-EDDnp), were selectively hydrolyzed by neutral endopeptidase (NEP, enkephalinase, neprilysin, EC 3.4.24.11) at the Arg-Leu and Arg-Phe bonds, respectively. The kinetic parameters for the NEP-catalyzed hydrolysis of Abz-<!-- $MVD$:face("Times") -->DRRL-EDDnp and Abz-<!-- $MVD$:face("Times") -->DRRF-EDDnp were Km = 2.8 µM, kcat = 5.3 min-1, kcat/Km = 2 min-1 µM-1 and Km = 5.0 µM, kcat = 7.0 min-1, kcat/Km = 1.4 min-1 µM-1, respectively. The high specificity of these substrates was demonstrated by their resistance to hydrolysis by metalloproteases [thermolysin (EC 3.4.24.2), angiotensin-converting enzyme (ACE; EC 3.4.24.15)], serineproteases [trypsin (EC 3.4.21.4), <!-- $MVD$:face("Symbol") --><FONT FACE="Symbol">a</font>-chymotrypsin (EC 3.4.21.1)] and proteases present in tissue homogenates from kidney, lung, brain and testis. The blocked amino- and carboxyl-terminal amino acids protected these substrates against the action of aminopeptidases, carboxypeptidases and ACE. Furthermore, <!-- $MVD$:face("Times") -->DR amino acids ensured total protection of Abz-<!-- $MVD$:face("Times") -->DRRL-EDDnp and Abz-<!-- $MVD$:face("Times") -->DRRF-EDDnp against the action of thermolysin and trypsin. Leu-EDDnp and Phe-EDDnp were resistant to hydrolysis by <!-- $MVD$:face("Symbol") --><FONT FACE="Symbol">a</font>-chymotrypsin. The high specifity of these substrates suggests their use for specific NEP assays in crude enzyme preparations