Characterization of the amylase activity present in larval extracts of two potato pest moths: Tecia solanivora and Symmetrischema tangolias

Main Article Content

Patricia Mora Criollo
Andrea Rodríguez Guerra
Carlos Soria

Abstract

Tecia solanivora and Symmetrischema tangolias (Lepidoptera: Gelechiidae) moths cause serious damage to Solanum tuberosum tubercles. The purpose of this study was to isolate and biochemically characterize amilases present in different larval moth stages. Soluble proteins were extracted from the larval stages raised in the laboratory. Differences in protein concentration were determined by spectrophotometry. Average weight for each larvae was calculated. T. solanivora was heavier and more soluble protein was extracted as compared with S. tangolias. Amilase activity of the different protein extracts was identified using starch degradation techniques. The amylasic activity of the IV stage of T. solanivora and S. tangolias incubated at different intervals of time were found to react different, however the results became similar when the activity of both extracts was scored after 72 h time reaction. Eleven protein bands between 225 and 10 kDa were identified electrophoretically. Among these bands, amylases were identified in both species in the 4 different stages in accordance to the molecular weights equivalent to 50 kDa. The protein bands of this enzyme were more defined in the I and II than in the III and IV stages, where they appeared quite diffused. Amylase activity was not linked to soluble protein concentrations; instead, it depended on reaction conditions. These results suggest the possibility of designing new forms of biocontrol against potato moths

Downloads

Download data is not yet available.

Article Details

How to Cite
1.
Mora Criollo P, Rodríguez Guerra A, Soria C. Characterization of the amylase activity present in larval extracts of two potato pest moths: Tecia solanivora and Symmetrischema tangolias. REMCB [Internet]. 2017 Aug. 14 [cited 2026 Sep. 6];34(1-2):113-27. Available from: https://remcb-puce.edu.ec/remcb/article/view/239
Section
Artículos Científicos

References

Agudelo C D, Corena-Mcleo M y Robledo S M. 2010. Anhidrasa Carbónica de Plasmodium falciparum: un blanco útil para el diseño de medicamentos antimaláricos y compuestos bloquea-dores de la transmisión de Malaria. Vitae, Revista de la Facultad de Química Farmacéutica, 17(1): 91–100.

Álvarez C. 2003. Actividad enzimática digestiva y evaluación de dietas para el destete de larvas de la cabrilla arenera Paralabrax maculatofasciatus (Percoide: Serranidae). Tesis para obtener el grado de doctor en Ciencias Marinas. Instituto Politécnico Nacional, Departamento de Desarrollo de Tecnologías. Baja California, EEUU.

Astudillo Y y Soria C A. 2011. Identificación y caracterización de carbohidratos y proteínas en las secreciones del dorso y del pie del molusco Limax flavus. Revista Ecuatoriana de Medicina y Ciencias Biológicas, 22: 33–48.

Baker J E. 1991. Purification and partial characterization of a amylase allozymes from the lesser grain borer Rhyzorpertha dominica. Insect Biochemistry, 21: 303–311.

Baker J E. 1983. Properties of Amylases from midguts of larvae of Sitophilus zeamais and Sitophilus granarius. Insect Biochemistry, 13(4): 421–428.

Barragán A R. 2005.Identificación, Biología y comportamiento de las polillas de la papa en el Ecuador. PROMSA-MAG, PUCE. 12 pp. ISBN 9978–77–124–7. Quito, Ecuador.

Cadena M, Naranjo A, Ñústez C E. 2005. Evaluación de la respuesta de 60 genotipos de Solanum phureja (Juz. et Buk.) al ataque de la Polilla gua-temalteca (Tecia solanivora Povolny). Agronomía Colombiana, 23 (1).

Campos F A P, Xavier-Filho J, Sila C P y Ary M B. 1989. Resolution and partial characterization of proteinases and amylases from midguts of lar-vae of the Bruchid Beetle Calloso-bruchus maculates (F). Comparative Biochemistry and Physiology, 92B(1): 51–57.

Childress C C y Sacktor B. 1970. Regulation of glycogen metabolism in insect flight muscle. Purification and properties of phospholylases in vitro and in vivo. The Journal of Biological Chemistry, 245: 2927–2936.

Da Lage J L, Wormhoudt A V y Cariou M L. 2002. Diversity and in animals, Review, Biologia, Bratislava, 57(11): 181–189.

Darvishzadeh A, Bandani A R, Karimi J y Timouri G. 2012. Biochemical characterisation of digestive a-amylase of Red Palm Weevil, Rhynchophorus ferrugineus (Olivier, 1790) (Coleoptera: Curculionidae), Archives of Phytopathology and Plant Protection, 45(18): 2132–2142.

Domínguez J, Carrero C, Ramírez W, Segovia P y Pino, H. 2009. Evaluación del efecto de insecticidas sobre larvas de Tecia solanivora.Agricultura Andina, 17: 61–73.

Herrera M. 2010. Interacciones intra e inter-específicas entre polillas de la papa (Lepidoptera: Gelechiidae).Tesis de Licenciatura en Ciencias Biológicas, Pontificia Universidad Católica del Ecuador. Quito, Ecuador.

Herrera F. 1998. La polilla guatemalteca de la papa. Biología, comportamiento y prácticas de manejo integrado. CORPOICA. Programa Regional Agrícola. p. 14.

Janecek S, Svensson B y Henrissat B. 1997. Domain evolution in the a amylase family. Journal of Molecular Evolution, New York, 45: 322–331.

Kazzazi M, Bandani A R y Hosseinkhani S. 2005. Biochemical characterization of a-amylase of the Sunn pest, Eurygaster integriceps.Entomological Science, 8, 371–377.

Kotkar H M, Bhide A J, Gupta V S y Giri A P. 2012. Amylase gene expression patterns in Helicoverpa armigera upon feeding on a range of host plants. Elsevier, Gene 501: 1–7.

Lagnaoui A, Cañedo V y Douches S D. 2000. Evaluation of Bt-cry1Ia1 (cryV) transgenic potatoes on two species of potato tuber moth, Phthorimaea operculella and Symmetrischema tangolias (Lepidoptera: Gelechiidae) in Peru. CIP Program Report 1999–2000, 117–121.

Ngernyuang N, Kobayashi I, Promboon A, Ratanapo S, Tamura T y Ngernsiri L. 2010. Cloning and expression analysis of the Bombyx mori α-amylase gene (Amy) from the indigenous Thai silkworm strain, Nanglai. Journal of Insect Science, 11(38): 1–16.

Raymond P H. 1984. The role of carbonic anhydrase in blood ion and acid-base regulation. American Zoologist, 24(1): 241–251.

Rodríguez-Guerra A, Barnes C, Ordóñez M E, Salazar A, Soria CA. 2012. Identificación y evaluación de algunos hongos con actividad celulásica aislados en Ecuador. Revista Ecuatoriana de Medicina y Ciencias Biológicas, 23: 65–81.

Schwartz L, Jones M, Kosz L, Kuah K. 1993. Selective repression of actin and myosin heavy chain expression during the programmed death of insect skeletal muscle. Developmental Biology, 158(2): 448–455.

Trujillo E, Ríos D, Cabrera R. 2002. Distribución de Tecia solanivora (Polvoni) (Lepidoptera: Gelechiidae) en Tenerife, Islas Canarias, España. Avances en investigación y manejo integrado de la polilla gualtemalteca de la papa, Tecia solanivora.Memorias del II taller Internacional de polilla gualtemalteca, Quito, Ecuador, 191–192.

Valderrama A M, Velásquez N, Rodríguez E, Zapata A, Zaidi M Z, Altosaar I y Arango R. 2007. Resistence to Tecia solanivora in three transgenic An-dean varieties of potato expressing Bacillus thuringiensis Cry1Ac pro-tein. Journal of Economic Entomology, 100(1): 172–179.

Valencia-Jiménez A, Arboleda V, López Ávila M F y Grosside-Sá. 2008. Digestive alpha-amylases from Tecia solanivora larvae (Lepidoptera: Gelechiidae): response to pH, temperature and plant amylase inhibitors. Bulletin of Entomological Research, 98: 575–579.

Vargas B I, Rubio S A y López-Avila A. 2004. Estudios de hábitos y comportamiento de la polilla guatemalteca Tecia solanivora (Lepidoptera: Gelechiidae) en papa almacenada. Revista Colombiana de Entomología,30(2): 1–4.

Viktorinova I, Kucerova L, Bohmova M, Henry I, Jindra M, Dolezal P, Zurovcova M y Zurovec M. 2011. Characterization of two closely related a-amylase paralogs in the bark beetle, Ips typographus (L.). Archives of Insect Biochemistry and Physiology, 77(4): 179–198.