Efeito de pós vegetais sobre sitophilus zeamais (mots., 1855) (coleoptera: curculionidae) / Effect of plant powders on Sitophilus zeamais (mots., 1855) (Coleoptera: Curculionidae)

Objetivou-se testar a atividade inseticida de pós vegetais em Sitophilus zeamais. Foram testados os pós de Anadenanthera colubrina (folhas); Annona muricata (sementes); Azadirachta inidica (folhas e flores); Caesalpinia pyramidalis (folhas), Chenopodium ambrosioides (folhas e flores); Cymbopogon sp.(folhas); Cymbopogon citratus (folhas); Momordica charantia (folhas e frutos); Piper nigrum (sementes); e Ricinus communis (folhas). Além disso, avaliou-se o potencial inseticida de folhas e flores de C. ambrosioides em diferentes dosagens. Na avaliação de repelência foi estabelecido um índice de preferência, e utilizado o teste t para comparação das médias das espécies vegetais. Também foi realizada a comparação das médias das plantas que foram classificadas como repelentes. Para avaliação da mortalidade, procedeu-se a análise de variância e a comparação das médias pelo teste de Tukey e também o teste t para comparação das médias dos tratamentos C. ambrosioides e P. nigrum. Os dados de emergência foram analisados pelo teste de Tukey. Para avaliar os dados de mortalidade, ocasionados por C. ambrosioides, determinou-se a CL50 utilizando a análise de Probit. Os dados de emergência foram verificados pela análise de regressão. As plantas que provocaram repelência foram Cymbopogon sp., C. citratus e C. ambrosioides. A planta que mais afetou a sobrevivência da praga foi C. ambrosioides, que provocou mortalidade total dos insetos infestantes e nenhuma emergência. Adultos de S. zeamais são mais suscetíveis a concentração de 0,125 g do pó de C. ambrosioides.

Effect of plant powders on Sitophilus zeamais (Mots., 1855) (Coleoptera: Curculionidae). The objective of the present study was to test the insecticidal activity of vegetable powders on Sitophilus zeamais. Powders of Anadenanthera colubrina (leaves); Annona muricata (seed); Azadirachta inidica(leaves and flowers);Caesalpinia pyramidalis(leaves);Chenopodium ambrosioides (leaves and flowers);Cymbopogon sp. (leaves);Cymbopogon citratus (leaves); Momordica charantia (leaves and fruits);Piper nigrum (seed); andRicinus communis (leaves) were evaluated. In addition, we evaluated the insecticidal potential of leaves and flowers of C. ambrosioidesat different dosages. In the evaluation of repellency a preference index was established, and the t test was used to compare the means of plant species. The means of plants that were classified as repellent were also compared. To assess mortality, we proceeded with the analysis of variance and comparison of means by Tukey test and also the t test for comparing the means of the C. ambrosioides and P. nigrum treatments. The emergence data were analyzed by Tukey test. To evaluate the data on mortality caused by C. ambrosioides, the CL50 was determined using Probit analysis. The emergence data were verified by regression analysis. Plants that caused repellency were Cymbopogon sp., C. citratusand C. ambrosioides. The plant that most affected the survival of the pest wasC. ambrosioides, which caused total mortality of insect infestations and no adult emergence. Adults of S. zeamaisare most susceptible to the concentration of 0.125 g ofC. ambrosioides powder.

Analysis of DNA polymerase activity in vitro using non-radioactive primer extension assay in an automated DNA sequencer

Although different DNA polymerases have distinct functions and substrate affinities, their general mechanism of action is similar. Thus, they can all be studied using the same technical principle, the primer extension assay employing radioactive tags. Even though fluorescence has been used routinely for many years for DNA sequencing, it has not been used in the in vitro primer extension assay. The use of fluorescence labels has obvious advantages over radioactivity, including safety, speed and ease of manipulation. In the present study, we demonstrated the potential of non-radioactive in vitro primer extension for DNA polymerase studies. By using an M13 tag in the substrate, we can use the same fluorescent M13 primer to study different substrate sequences. This technique allows quantification of the DNA polymerase activity of the Klenow fragment using different templates and under different conditions with similar sensitivity to the radioactive assay.