Metabolism of hydrogen peroxide in univoltine and polyvoltine strains of silkworm (Bombyx mori)

Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology

Volumn 152, Issue 4, 2009, Pages 339-345

  Zhao, Linchuan ^a,b   Shi, Liangen ^a  

^a ZHEJIANG UNIVERSITY   (China)

^b SOOCHOW UNIVERSITY   (China)

Author keywords

Bombyx mori; Catalase; Diapause; Hydrogen peroxide; Polyvoltine strain; Superoxide dismutase; Univoltine strain; Xanthine oxidase

Indexed keywords

CATALASE; DIAPAUSE HORMONE; HYDROGEN PEROXIDE; PEPTIDE HORMONE; SUPEROXIDE DISMUTASE; UNCLASSIFIED DRUG; XANTHINE OXIDASE;

ANIMAL EXPERIMENT; ARTICLE; DIAPAUSE; EMBRYO DEVELOPMENT; ENZYME ACTIVITY; GENE EXPRESSION; MULTIVOLTINE ORGANISM; NONHUMAN; PAEDOGENESIS; PRIORITY JOURNAL; SILKWORM; UNIVOLTINE ORGANISM;

BOMBYX MORI; MAMMALIA;

EID: 60649118905     PISSN: 10964959     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbpb.2008.12.014     Document Type: Article

References (30)

1. Biebert G.P., Schjoerring J.K., and Jahn T.P. Membrane transport of hydrogen peroxide. Biochim. Biophys. Acta 1758 (2006) 994-1003
2. Cumming R.C., Andon N.L., Haynes P.A., Park M., Fisher W.H., and Schubert D. Protein disulfide bond formation in the cytoplasm during oxidative stress. J. Biol. Chem. 279 (2004) 21749-21758
3. Dalton T.P., Shertzer H.G., and Puga A. Regulation of gene expression by reactive oxygen. Annu. Rev. Pharmacol. Toxicol. 39 (1999) 67-101
4. Felton G.W., and Summers C.B. Antioxidant systems in insects. Arch. Insect Biochem. Physiol. 29 (1995) 187-197
5. Grubor-Lajsic G., Block W., Telesmanic M., Jovanovic A., Stevanovic D., and Baca F. Effect of cold acclimation on the antioxidant defense system of two larval Lepidoptera (Noctuidae). Arch. Insect Biochem. Physiol. 36 (1997) 1-10
6. Hermes-Lima M., and Zenteno-Savin T. Animal response to drastic changes in oxygen availability and physiological oxidative stress. Comp. Biochem. Physiol. C 133 (2002) 537-556
7. Hofmann B., Hecht H.J., and Flohe L. Peroxiredoxins. Biol. Chem. 383 (2002) 347-364
8. Homma T., Watanabe K., Tsurumaru S., Kataoka H., Imai K., Kamba M., Niimi T., Yamashita O., and Yaginuma T. G protein-coupled receptor for diapause hormone, an inducer of Bombyx embryonic diapause. Biochem. Biophys. Res. Commun. 344 (2006) 386-393
9. Horie Y., Kanda T., and Mochida Y. Sorbitol as an arrester of embryonic development in diapausing eggs of the silkworm, Bombyx mori. J. Insect Physiol. 46 (2000) 1009-1016
10. Javanovic-Galović A., Blagojević D.P., Grubor-Lajšić G., Worland R., and Spasić M.B. Role of antioxidant defense during different stages of preadult life cycle in European corn borer (Ostrinia nubilalis, Hubn.): diapaus and metamorphosis. Arch. Insect Biochem. Physiol. 55 (2004) 79-89
11. Kitagawa N., Shiomi K., Imai K., Niimi T., Yaginuma T., and Yamashita O. Establishment of a sandwich ELISA system to detect diapause hormone and development profile of hormone levels in egg and suboesophageal ganglion of the silkworm, Bombyx mori. Zool. Sci. 22 (2005) 213-221
12. Kitagawa N., Shiomi K., Imai K., Niimi T., Yamashita O., and Yaginuma T. Diapause hormone levels in suboesophageal ganglia of uni-, bi, and poly-voltine races during pupal-adult development of Bombyx mori, and the effects of ouabain, an inhibitor of Na+-K+ ATPase, on the hormone levels. J. Insect Biotechnol. Sericology 74 (2005) 57-62
13. Katagiri N., Ando O., and Yamashita O. Reduction of glycogen in eggs of the silkworm, Bombyx mori, by use of a trehalase inhibitor, trehazolin, and diapause induction in glycogen-reduced eggs. J. Insect Physiol. 44 (1998) 1205-1212
14. Kristensen B.K., Askerlund P., Bykova N.V., Egsgaard H., and Moller I.M. Identification of oxidized proteins in the matrix of rice leaf mitochondria by immunoprecipitation and two-dimensional liquid chromatograph-tandem mass spectrometry. Phytochemistry 65 (2004) 1839-1851
15. Landar A., Oh J.Y., Giles N.M., Isom A., Kirk M., Barnes S., and Darley-Usmar V.M. A sensitive method for the quantitative measurement of protein thiol modification in response to oxidative stress. Free Radical Biol. Med. 40 (2006) 459-468
16. Mathews M.C., Summers C.B., and Felton G.W. Ascorbate peroxidase-a novel antioxidant enzyme in insects. Arch. Insect Biochem. Physiol. 34 (1997) 57-68
17. Morita A., Niimi T., and Yamashita O. Physiological differentiation of DH-PBAN-producing neurosecretory cells in the silkworm embryo. J. Insect Physiol. 49 (2003) 1093-1102
18. Ohtsuki Y. Silkworm eggs. In: Japanese Society of Sericultural Science (Ed). A General Textbook of Sericulture (1979), Nihon Sansei Shinbun-Sha, Tokyo 156-173
19. Rhee S.G., Chae H.Z., and Kim K. Peroxiredoxins: a historical overview and speculative preview of novel mechanisms and emerging concepts in cell signaling. Free Radical Biol. Med. 38 (2005) 1543-1552
20. Shen A.Y., Zhao L.C., and Liu H.T. Diapausing eggs of the silkworm, Bombyx mori, activated by exogenous hydrogen peroxide. Acta Sericol. Sin. 29 (2003) 311-313
21. Su Z.H., Ikeda M., Sato Y., Saito H., Imai H., and Yamashita O. Molecular characterization of ovary trehalase of the silkworm, Bombyx mori and its transcriptional activation by diapause hormone. Biochim. Biophys. Acta 1218 (1994) 366-374
22. Suzuki Y.J., Forman H.J., and Sevanian A. Oxidants as stimulations of signal transduction. Free Radical Biol. Med. 22 (1997) 269-285
23. Switala J., and Loewen P.C. Diversity of properties among catalases. Arch. Biochem. Biophys. 401 (2002) 145-154
24. Wang Q., Chen K.P., Zhao Y., Li Y.J., Shen H.X., and Mu R.H. Identification and characterization of a novel 1-Cys peroxiredoxin from silkworm, Bombyx mori. Comp. Biochem. Physiol. B 149 (2008) 176-182
25. Yaginuma T., and Yamashita O. Oxygen consumption in relation to sorbitol utilization at the termination of diapause in eggs of the silkworm, Bombyx mori. J. Insect Physiol. 45 (1999) 621-627
26. Yamamoto K., Banno Y., Fujii H., Miake F., Kashige N., and Aso Y. Catalase from the silkworm, Bombyx mori: gene sequence, distribution, and overexpression. Insect Biochem. Mol. Biol. 35 (2005) 277-283
27. Yamashita O. Diapause hormone of the silkworm, Bombyx mori: structure, gene expression and function. J. Insect Physiol. 42 (1996) 669-679
28. Yamashita, O., Yaginuma, T., 1991. Silkworm eggs at low temperatures: implications for sericulture. In: Lee, R.E. Jr., Denlinger, D.L. (Eds.), Insects at low temperature. Chapman and Hall, New York, pp. 424-445.
29. Zhao L.C., Sima Y.H., and Shen X.M. Metabolism of hydrogen peroxide in the course of embryonic development in silkworm. Dev. Reprod. Biol. 8 (1999) 41-48
30. Zhao L.C., Sima Y.F., Li B., and Shen X.M. Effect of hydrocholoric acid on the metabolism of hydrogen peroxide during embryonic development of Bombyx. Acta Sericol. Sin. 26 (2000) 268-270