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Journal of Environmental BiologypISSN: 0254-8704 ; eISSN: 2394-0379 ; CODEN: JEBIDP |
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Abstract - Issue July 2009, 30 (4) BackEffects of Indian coral tree, Erythrina indica lectin on eggs and larval development of melon fruit fly, Bactrocera cucurbitae Kuljinder Singh1, Manpreet Kaur2,
Pushpinder J. Rup1 and Jatinder
Singh2 1Insect Physiology Laboratory, Department of Zoology, 2Protein
Laboratory, Department of Molecular Biology and Biochemistry, (Received:
Abstract: Present study was undertaken to
investigate the influence of D-galactose binding lectin from Erythrina indica Lam. on the eggs and second instar
larvae (64-72 hr) of melon fruit fly, Bactrocera cucurbitae (Coquillett). The lectin from E. indica seeds was
extracted and purified by affinity chromatography using asilofetuin
linked porous amino activated silica beads. The effects of various
concentrations (0, 125, 250, 500 and 1000 ?g ml-1) of lectin were studied on freshly laid eggs (0-8 hr) of B. cucurbitae which showed non-significant reduction in
percent hatching of eggs.? However, the
treatment of second instar larvae (64-72 hr) with
various test concentrations (0, 25, 50, 100 and 200 ?g ml-1) of lectin significantly reduced the percent pupation and
percent emergence of B. cucurbitae depicting a
negative correlation with the lectin concentration.
The LC50 (81?g ml-1) treatment significantly decreased
the pupal weight. Moreover, the treatment of larvae
had also induced a significant increase in the remaining development duration.
The activity of three hydrolase enzymes (esterases,
acid and alkaline phosphatases), one oxidoreductase (catalase) and one
group transfer enzyme (glutathione S-transferases)
was assayed in second instar larvae under the
influence of LC50 concentration of lectin
for three exposure intervals (24, 48 and 72 hr). It significantly suppressed
the activity of all the enzymes after all the three exposure intervals except
for esterases which increased significantly. Key
words: Lectin,
Erythrina indica, Bactrocera cucurbitae,
Development, Esterases, Phosphatases,
Catalase, Transferases ?????? PDF of full length paper
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of the data, and the acceptability of the conclusions enforced or derived, rest
completely with the author(s). |