RESUMEN
Anagasta kuehniella is a polyphagous pest that causes economic losses worldwide. This species produces serine proteases as its major enzymes for protein digestion. In this study, a new serine-protease inhibitor was isolated from Acacia polyphylla seeds (AcKI).Further analysis revealed that AcKI is formed by two polypeptide chains with a relative molecular mass of â¼20 kDa. The effects of AcKI on the development, survival, and enzymatic activity of Anagasta kuehniella larvae were evaluated, by incorporating AcKI in an artificial diet. Bioassays revealed a reduction in larval weight of â¼50% with the lower concentration of AcKI used in the study (0.5%). Although additionalassays showed an increase in endogenous trypsin and chymotrypsin activities, with a degree of AcKI-insensivity, AcKI produces an anti nutritional effect on A. kuehniella, indicating AcKI as a promising bioinsecticide protein for engineering plants that are resistant to insect pests.
Asunto(s)
Acacia/química , Insecticidas/aislamiento & purificación , Mariposas Nocturnas/efectos de los fármacos , Péptidos/aislamiento & purificación , Proteínas de Plantas/aislamiento & purificación , Semillas/química , Secuencia de Aminoácidos , Animales , Digestión/efectos de los fármacos , Insecticidas/química , Insecticidas/farmacología , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Larva/fisiología , Datos de Secuencia Molecular , Mariposas Nocturnas/crecimiento & desarrollo , Mariposas Nocturnas/fisiología , Péptidos/química , Péptidos/farmacología , Proteínas de Plantas/química , Proteínas de Plantas/genética , Proteínas de Plantas/farmacología , Alineación de Secuencia , Inhibidores de Serina Proteinasa/química , Inhibidores de Serina Proteinasa/genética , Inhibidores de Serina Proteinasa/aislamiento & purificación , Inhibidores de Serina Proteinasa/farmacologíaRESUMEN
The objective of this work was to study the insecticidal effect of labramin, a protein that shows lectin-like properties. Labramin was isolated from seeds of the Beach Apricot tree, Labramia bojeri A. DC ex Dubard (Ericales: Sapotaceae), and assessed against the development of the Mediterranean flour moth Ephestia kuehniella Zeller (Lepidoptera: Pyralidae), an important pest of stored products such as corn, wheat, rice, and flour. Results showed that labramin caused 90% larval mortality when incorporated in an artificial diet at a level of 1% (w/w). The presence of 0.25% labramin in the diet affected the larval and pupal developmental periods and the percentage of emerging adults. Treatments resulted in elevated levels of trypsin activity in midgut and fecal materials, indicating that labramin may have affected enzyme-regulatory mechanisms by perturbing peritrophic membranes in the midgut of is. kuehniella larvae. The results of dietary experiments with E. kuehniella larvae showed a reduced efficiency for the conversion of ingested and digested food, and an increase in approximate digestibility and metabolic cost. These findings suggest that labramin may hold promise as a control agent to engineer crop plants for insect resistance.
Asunto(s)
Insecticidas/aislamiento & purificación , Mariposas Nocturnas/efectos de los fármacos , Extractos Vegetales/química , Lectinas de Plantas/aislamiento & purificación , Sapotaceae/química , Animales , Ingestión de Alimentos/efectos de los fármacos , Electroforesis en Gel de Poliacrilamida , Femenino , Insecticidas/toxicidad , Larva/efectos de los fármacos , Mariposas Nocturnas/enzimología , Mariposas Nocturnas/crecimiento & desarrollo , Extractos Vegetales/toxicidad , Lectinas de Plantas/toxicidad , Proteínas de Plantas/aislamiento & purificación , Proteínas de Plantas/toxicidad , Semillas/química , Tripsina/metabolismoRESUMEN
The aim of this work was to investigate the potential of castor oil for the control of papaya diseases caused by the fungus Colletotrichum gloeosporioides and the bacterium Pseudomonas caricapapayae. The treatment with 1% castor oil did not significantly affect the fungal growth. The effectiveness of castor oil for the control of anthracnose was shown when 5% and 10% (v/v) were used in the assays resulting in reduced mycelial growth. Fungal sporulation was strongly inhibited at 10% (v/v) concentration of essential oil. The studies with the fresh fruits treated with 5% (v/v) castor oil in aqueous emulsions resulted in effective reduction of pathogen spread in these fruits. No lesion was found in the fruits treated with oil, when compared to the control fruits. Castor oil showed no effect against the P. caricapapayae when tested in vitro. These results suggested the potential use of the castor bean essential oil and its fatty acids constituents for the control of anthracnose in papaya fruits.
RESUMEN
Digestive endoprotease activities of the coconut palm weevil, Homalinotus coriaceus (Coleoptera: Curculionidae), were characterized based on the ability of gut extracts to hydrolyze specific synthetic substrates, optimal pH, and hydrolysis sensitivity to protease inhibitors. Trypsin-like proteinases were major enzymes for H. coriaceus, with minor activity by chymotrypsin proteinases. More importantly, gut proteinases of H. coriaceus were inhibited by trypsin inhibitor from Inga laurina seeds. In addition, a serine proteinase inhibitor from I. laurina seeds demonstrated significant reduction of growth of H. coriaceus larvae after feeding on inhibitor incorporated artificial diets. Dietary utilization experiments show that 0.05% I. laurina trypsin inhibitor, incorporated into an artificial diet, decreases the consumption rate and fecal production of H. coriaceus larvae. Dietary utilization experiments show that 0.05% I. laurina trypsin inhibitor, incorporated into an artificial diet, decreases the consumption rate and fecal production of H. coriaceus larvae. We have constructed a three-dimensional model of the trypsin inhibitor complexed with trypsin. The model was built based on its comparative homology with soybean trypsin inhibitor. Trypsin inhibitor of I. laurina shows structural features characteristic of the Kunitz type trypsin inhibitor. In summary, these findings contribute to the development of biotechnological tools such as transgenic plants with enhanced resistance to insect pests.
Asunto(s)
Fabaceae , Proteínas de Insectos/fisiología , Péptido Hidrolasas/fisiología , Péptidos/farmacología , Proteínas de Plantas/farmacología , Gorgojos/enzimología , Secuencia de Aminoácidos , Animales , Sistema Digestivo/enzimología , Proteínas de Insectos/aislamiento & purificación , Proteínas de Insectos/farmacología , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Modelos Moleculares , Datos de Secuencia Molecular , Inhibidores de Proteasas/farmacología , Estructura Terciaria de Proteína , Alineación de Secuencia , Homología Estructural de Proteína , Gorgojos/efectos de los fármacos , Gorgojos/crecimiento & desarrolloRESUMEN
Anagasta kuehniella is a polyphagous pest that feeds on a wide variety of stored products. The possible roles suggested for seed proteinase inhibitors include the function as a part of the plant defensive system against pest via inhibition of their proteolytic enzymes. In this study, a trypsin inhibitor (ApTI) was purified from Adenanthera pavonina seed and was tested for insect growth regulatory effect. The chronic ingestion of ApTI did result in a significant reduction in larval survival and weight. Larval and pupal developmental time of larvae fed on ApTI diet at 1% was significantly longer; the larval period was extended by 5 days and pupal period was 10 days longer, therefore delaying by up to 20 days and resulting in a prolonged period of development from larva to adult. As a result, the ApTI diet emergence rate was only 28% while the emergence rate of control larvae was 80%. The percentage of surviving adults (%S) decreased to 62%. The fourth instar larvae reared on a diet containing 1% ApTI showed a decrease in tryptic activity of gut and that no novel proteolytic form resistant to ApTI was induced. In addition, the tryptic activity in ApTI -fed larvae was sensitive to ApTI. These results suggest that ApTI have a potential antimetabolic effect when ingested by A. kuehniella.
Asunto(s)
Fabaceae/química , Lepidópteros/efectos de los fármacos , Inhibidores de Tripsina/farmacología , Animales , Ingestión de Alimentos/efectos de los fármacos , Larva/efectos de los fármacos , Larva/enzimología , Larva/crecimiento & desarrollo , Lepidópteros/enzimología , Lepidópteros/crecimiento & desarrollo , Control Biológico de Vectores/métodos , Semillas/químicaRESUMEN
A novel trypsin inhibitor (PFTI) was isolated from Plathymenia foliolosa (Benth.) seeds by gel filtration chromatography on a Sephadex G-100, DEAE-Sepharose, and trypsin-Sepharose columns. By SDSPAGE, PFTI yielded a single band with a M(r) of 19 kDa. PFTI inhibited bovine trypsin and bovine chymotrypsin with equilibrium dissociation constants (K(i)) of 4 x 10(-8) and 1.4 x 10(-6) M, respectively. PFTI retained more than 50% of activity at up to 50 degrees C for 30 min, but there were 80 and 100% losses of activity at 60 and 70 degrees C, respectively. DTT affected the activity or stability of PFTI. The N-terminal amino acid sequence of PFTI showed a high degree of homology with various members of the Kunitz family of inhibitors. Anagasta kuehniella is found worldwide; this insect attacks stored grains and products of rice, oat, rye, corn, and wheat. The velvet bean caterpillar (Anticarsia gemmatalis) is considered the main defoliator pest of soybean in Brazil. Diatraea saccharalis, the sugar cane borer, is the major pest of sugar cane crops, and its caterpillar-feeding behavior, inside the stems, hampers control. PFTI showed significant inhibitory activity against trypsin-like proteases present in the larval midguts on A. kuehniella and D. saccharalis and could suppress the growth of larvae.
Asunto(s)
Fabaceae/química , Proteínas de Plantas/química , Proteínas de Plantas/aislamiento & purificación , Semillas/química , Inhibidores de Tripsina/química , Inhibidores de Tripsina/aislamiento & purificación , Secuencia de Aminoácidos , Fabaceae/genética , Fabaceae/metabolismo , Cinética , Datos de Secuencia Molecular , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Semillas/genética , Semillas/metabolismo , Alineación de Secuencia , Inhibidores de Tripsina/genética , Inhibidores de Tripsina/metabolismoRESUMEN
Plants synthesize a variety of molecules, including proteinaceous proteinase inhibitors, to defend themselves of being attacked by insects. In this work, a novel trypsin inhibitor (PPTI) was purified from the seeds of the native Brazilian tree Poecilanthe parviflora (Benth) (Papilioinodeae, Leguminosae) by gel filtration chromatography on a Sephadex G-100 followed by Superdex G75 chromatography (FPLC), Sepharose 4B-Trypsin column, and fractionated by reversed-phase HPLC on a C-18 column. SDS-PAGE showed that PPTI consisted of a single polypeptide chain with molecular mass of about 16 kDa. The dissociation constant of 1.0 x 10(-7) M was obtained with bovine trypsin. PPTI was stable over a wide range of temperature and pH and in the presence of DTT. The N-terminal sequence of the PPTI showed a high degree of homology with other Kunitz-type inhibitors. Trypsin-like activity in midguts of larval Diatraea saccharalis, Anagasta kuehniella, Spodoptera frugiperda, and Corcyra cephalonica were substantially inhibited by PPTI.
Asunto(s)
Fabaceae/química , Tracto Gastrointestinal/enzimología , Control de Insectos , Mariposas Nocturnas/enzimología , Péptido Hidrolasas/química , Semillas/química , Inhibidores de Tripsina/química , Inhibidores de Tripsina/aislamiento & purificación , Animales , Cromatografía Liquida , Concentración de Iones de Hidrógeno , Peso Molecular , Mariposas Nocturnas/efectos de los fármacos , Temperatura , Inhibidores de Tripsina/farmacologíaRESUMEN
Plant lectins have insecticidal activity that is probably mediated through their ability to bind carbohydrates. To examine the influence of sugars on the insecticidal activity of a lectin from Talisia esculenta seeds (TEL), the lectin was mixed with mannose, glucose, or mannose plus glucose. Mannose abolished the insecticidal activity. Affinity chromatography showed that TEL bound to midgut proteins of the insect Callosobruchus maculatus. Immunoblotting showed that TEL recognized some proteins, probably glycoproteins, present in the midgut membrane of this insect. The principal proteases responsible for digestive proteolysis in fourth instar larvae of C. maculatus were purified by chromatography on activated thiol-Sepharose. These purified proteases were unable to digest TEL after a 15-h incubation. These results suggest that the insecticidal activity of TEL involves a specific carbohydrate-lectin interaction with glycoconjugates on the surface of digestive tract epithelial cells, as well as binding to assimilatory glycoproteins present in midgut extracts and resistance to enzymatic digestion by cysteine proteinases.
Asunto(s)
Escarabajos/efectos de los fármacos , Insecticidas/farmacología , Lectinas de Plantas/farmacología , Sapindaceae/química , Animales , Bioensayo/métodos , Peso Corporal , Carbohidratos/farmacología , Escarabajos/enzimología , Cisteína Endopeptidasas/metabolismo , Sistema Digestivo/enzimología , Insecticidas/antagonistas & inhibidores , Insecticidas/metabolismo , Mucosa Intestinal/metabolismo , Larva/efectos de los fármacos , Lectinas de Plantas/antagonistas & inhibidores , Lectinas de Plantas/metabolismo , Semillas/química , Análisis de SupervivenciaRESUMEN
The cowpea weevil Callosobruchus maculatus is one of the major pests of Vigna unguiculata cowpea. Digestion in the cowpea weevil is facilitated by high levels of cysteine and aspartic acid proteinases. Plants synthesize a variety of molecules, including proteinaceous proteinase inhibitors, to defend themselves against attack by insects. In this work, a trypsin inhibitor (ApTI) isolated from Adenanthera pavonina seeds showed activity against papain. The inhibition of papain by ApTI was of the noncompetitive type, with a K(i) of 1 microM. ApTI was highly effective against digestive proteinases from C. maculatus, Acanthoscelides obtectus (bean weevil), and Zabrotes subfasciatus (Mexican bean weevil) and was moderately active against midgut proteinases from the boll weevil Anthonomus grandis and the mealworm Tenebrio molitor. In C. maculates fed an artificial diet containing 0.25% and 0.5% ApTI (w/w), the latter concentration caused 50% mortality and reduced larval weight gain by approximately 40%. The action of ApTI on C. maculatus larvae may involve the inhibition of ApTI-sensitive cysteine proteinases and binding to chitin components of the peritrophic membrane (or equivalent structures) in the weevil midgut.
Asunto(s)
Escarabajos/enzimología , Fabaceae/química , Péptidos/aislamiento & purificación , Péptidos/farmacología , Proteínas de Plantas/aislamiento & purificación , Proteínas de Plantas/farmacología , Semillas/química , Animales , Quitina/metabolismo , Inhibidores de Cisteína Proteinasa/farmacología , Larva/enzimología , Papaína/antagonistas & inhibidoresRESUMEN
This study starts by isolating and characterizing the first protein from Labramia bojeri seeds, which belong to the Sapotaceae family. The purified lectin analyzed by SDS-PAGE with and without beta-mercaptoethanol shows two protein bands (M(r) = 19 and 20 kDa), which cannot be resolved. Protein bands have shown similar characteristics as molecular masses, determined by gel filtration and native gel; N-terminal sequences presented a difference in their isoelectric points. We have suggested that those protein bands might be variants of the protein named Labramin. The sequence database search has shown that the N-terminal sequence of Labramin presented a high degree of homology to Kunitz-type trypsin inhibitor (82-52%) despite no trypsin inhibition activity detection. The lectin-like form from Labramin was better inhibited by glycoproteins and has also presented growth inhibition of the fungus Colletotrichum lindemuthianum and the yeast Saccharomyces cerevisiae, but it has not presented an apparent effect on Fusarium oxysporum.
Asunto(s)
Péptidos/aislamiento & purificación , Lectinas de Plantas/aislamiento & purificación , Proteínas de Plantas/aislamiento & purificación , Sapotaceae/química , Semillas/química , Animales , Electroforesis en Gel de Poliacrilamida , Fungicidas Industriales/farmacología , Hemaglutinación , Humanos , Concentración de Iones de Hidrógeno , Péptidos/química , Lectinas de Plantas/química , Proteínas de Plantas/químicaRESUMEN
This study describes the purification of an N-acetylglucosamine-binding lectin from Koelreuteria paniculata seeds and its effects on the larval development of Callobruchus maculatus and Anagasta kuehniella. The lectin (KpLec) was characterized and isolated by gel filtration, affinity column, and reverse phase chromatography. SDS-PAGE indicated that this lectin is a dimer composed of subunits of 22 and 44 kDa. The N terminus exhibited 40% similarity with Urtiga dioica agglutinin. KpLec was tested for anti-insect activity against C. maculatus and A. kuehniella. With regard to C. maculatus, an artificial diet containing 0.7 and 1% KpLec produced LD(50) and ED(50) value, respectively. However, for A. kuenhiella, an artificial diet containing 0.65% KpLec produced an LD(50), whereas 0.2% KpLec produced an ED(50). The transformation of genes coding for this lectin could be useful in the development of insect resistance in important agricultural crops.