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Trehalase in the spermatophore from the bean-shaped accessory gland of the male mealworm beetle, Tenebrio molitor: purification, kinetic properties and localization of the enzyme

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Abstract

Trehalase from the bean-shaped accessory glands of the male mealworm beetle, Tenebrio molitor, was purified by acid treatment, with subsequent chromatography on columns of DEAE-cellulofine and Sephacryl S-300. The molecular masses of the native and the denatured forms were estimated to be 43 and 62 kDa by gel filtration and SDS-PAGE, respectively, an indication that the trehalase may be composed of a single polypeptide. The optimum pH of the reaction catalyzed by trehalase was 5.6–5.8. The K m for trehalose was 4.4 mmol·l−1. Immunohistochemical experiments with trehalase-specific antiserum showed that the enzyme was localized in one specific type of secretory cell in the bean-shaped accessory gland epithelium and within the semisolid secretory mass that was a precursor to the wall of spermatophore. SDS-PAGE and immunoblotting analysis revealed the presence of a polypeptide of about 62 kDa in the spermatophore, Immunohistochemical observations showed that the trehalase was located at the outgrowth in the anterior portion of the spermatophore. When a fresh spermatophore was immersed in phosphate-buffered saline it discharged sperm in the same manner as in the bursa copulatrix of the female. Before the rupture of the expanded bulb of the spermatophore, almost all of the trehalase had dissolved in the phosphate-buffered saline. The addition of validoxylamine A to the saline, a specific inhibitor of trehalase, did not affect the expansion and evacuation of the spermatophore. These results demonstrate that trehalase, synthesized by a specific type of secretory cell in the bean-shaped accessory gland epithelium, is actively passed into the lumen of the bean-shaped accessory gland and then incorporated into the spermatophore. Trehalase appears to be one of the structural proteins of the spermatophore, although the possibility can not yet be completely ruled out that the trehalase-trehalose system functions for the nourishment and/or activation of the sperm in the bursa copulatrix of the female.

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Abbreviations

BAG :

bean-shaped accessory gland(s)

DEAE :

diethylaminoethyl

Kpi buffer :

K2HPO4/KH2PO4 buffer (pH 7.0)

PAGE :

polyacrylamide gel electrophoresis

PBS :

phosphate-buffered saline

SDS :

sodium dodecy sulphate

Spph :

spermatophore(s)

TAG :

tubular accessory gland(s)

References

  • Asano N, Yamaguchi T, Kameda Y, Matsui K (1987) Effect of validomycins on glycohydrolases of Rhizooctonia solani J Antibiotics 40: 526–532

    Google Scholar 

  • Asano N, Takeuchi M, Kameda Y, Matsui K, Kono Y (1990) Trehalase inhibitors, yalidoxylamine A and related compounds as insecticides. J Antibiotics 43: 722–726

    Google Scholar 

  • Azuma M, Yamashita O (1985a) Cellular localization and proposed function of midgut trehalase in the silkworm, Bombyx mori. Tissue Cell 17: 539–551

    Google Scholar 

  • Azuma M, Yamashita O (1985b) Immunohistochemical and biochemical localization of trehalase in the developing ovaries of the silkworm, Bombyx mori. Insect Biochem 15: 589–596

    Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72: 248–254

    Google Scholar 

  • Dailey PJ, Happ GM (1983) Cytodifferentiation in the accessory glands of Tenebrio molitor. XI. Transitional cell types during establishment of pattern. J Morphol 178: 139–154

    Google Scholar 

  • Dailey PJ, Gadzama NM, Happ GM (1980) Cytodifferentiation in the accessory glands of Tenebrio molitor. VI. A congruent map of cells and their secretions in the layered elastic product of the male bean-shaped gland. J Morphol 166: 289–322

    Google Scholar 

  • Feldman-Muhsam B, Borut S, Saliternick-Givant S, Eden C (1973) On the evacuation of sperm from the spermatophore of the tick, Onithodorus savignyi J Insect Physiol 19: 951–962

    Google Scholar 

  • Forstner GG, Sabesin SM, Isselbacher KJ (1968) Rat intestinal microvillus membranes, purification and biochemical characterization. Biochem J 106: 381–390

    Google Scholar 

  • Friedman S (1975) Multiple forms of trehalase in Phormia regina. Partial purification, tissue specificities, some kinetic properties of adult enzymes. Insect Biochem 5: 151–164

    Google Scholar 

  • Gadzama NM, Happ GM (1974) The structure and evacuation of the spermatophore of Tenebrio molitor L (Coleoptera: Tenebrionidae). Tissue Cell 6: 95–108

    Google Scholar 

  • George SG, Kenny AJ (1973) Studies on the enzymology of purified preparations of brush border from rabbit kidney. Biochem J 134: 43–57

    Google Scholar 

  • Gilby AR, Wyatt SS, Wyatt GR (1967) Trehalases from the cockroach, Blaberus discoidalis: activation, solubilization and properties of the muscle enzyme and some properties of the intestinal enzymes. Acta Biochem Pol 14: 83–100

    Google Scholar 

  • Grimnes KA, Happ GM (1986) A monoclonal antibody against a structural protein in the spermatophore of Tenebrio molitor. Insect Biochem 16: 635–643

    Google Scholar 

  • Grimnes KA, Bricker CS, Happ GM (1986) Ordered flow of secretion from accessory glands to specific layers of the spermatophore of mealworm beetles: demonstration with a monoclonal antibody. J Exp Zool 240: 275–286

    Google Scholar 

  • Happ GM (1984) Structure and development of male accessory glands in insects. In: King RC, akai H (eds) Insect Ultrastructure, vol 2. Plenum Press, New York, pp 365–396

    Google Scholar 

  • Happ GM (1992) Maturation of the male reproductive system and its endocrine regulation. Annu Rev Entomol 37: 303–320

    Google Scholar 

  • Happ GM, MacLeod BJ, Szopa TM, Bricker CS, Lowell TC, Sankel JH, Yuncker C (1985) Cell cycles in the male accessory glands of mealworm pupae. Dev Biol 107: 314–324

    Google Scholar 

  • Huet C (1966) Etude experimentale du developpement de l'appareil genital male de Tenebrio molitor (Coleoptere Tenebrionide). C R Soc Biol 160: 2021–2025

    Google Scholar 

  • Ikeda M, Yaginuma T, Yamashita O (1991) Developmental profile and tissue localization of the protease responsible for vitellin degradation in the silkworm, Bombyx mori. J Seric Sci Jpn 60: 178–185

    Google Scholar 

  • Jahagirdar AP, Downer RGH, Viswanatha T (1990) Purification and characterization of trehalase-hydrolysing enzymes from thoracic musculature of the American cockroach, Periplaneta americana. Insect Biochem 20: 511–516

    Google Scholar 

  • Kameda Y, Asano N, Yamaguchi T, Matsui K (1987) Validoxylamines as trehalase inhibitors. J Antibiotics 40: 563–56

    Google Scholar 

  • Khalifa A (1949) The mechanism of insemination and mode of action of the spermatophore in Gryllus domesticus Q J Microsc Sci 90: 281–292

    Google Scholar 

  • Kono Y, Takahashi M, Matsushita K, Nishina M, Kameda Y, Hori E (1994) Inhibition of flight in Periplaneta americana (L.) by a trehalase inhibitor, validoxylamine A. J Insect Physiol 40: 455–461

    Google Scholar 

  • Laufer H, Nagase Y, Vanderberg J (1963) Nucleo-cytoplasmic interactions in the development of the salivary glands of Chironomus thummi. Biol Bull Mar Biol Lab Woods Hole 125: 359

    Google Scholar 

  • Lefevre YA, Huber RE (1970) Solubilization, purification, and some properties of trehalase from honey bee (Apis mellifera). Arch Biochem Biophys 140: 514–518

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with Folin phenol reagent. J Biol Chem 193: Biol Chem 193: 265–275

    Google Scholar 

  • Mann T (1984) Spermatophores. Development, structure, biochemical attributes and role in the transfer of spermatozoa. Springer, Berlin

    Google Scholar 

  • Nakano M (1980) Purification and properties of rabbit renal brush border membrane trehalase. Fed Proc 39: 1919

    Google Scholar 

  • Ogiso M, Shinohara Y, Hanaoka K, Takahashi SY (1982) Purification of trehalases from the male accessory glands of the American cockroach, Periplaneta americana Comp Biochem Physiol 72B: 511–515

    Google Scholar 

  • Ogiso M, Shinohara Y, Hanaoka K, Kageyama T, Takahashi SY (1985) Further purification and characterization of trehalases from the American cockroach, Periplaneta americana. J Comp Physiol B 155: 553–560

    Google Scholar 

  • Paesen GC, Schwartz MB, Peferoen M, Meyda F, Happ GM (1992) Amino acid sequence of Sp23, a structural protein of the spermatophore of the mealworm beetle, Tenebrio molitor J Biol Chem 267: 18852–18857

    Google Scholar 

  • Ruf J, Wacker H, James P, Maffia M, Seiler P, Galand G, von Kieckebusch A, Semenza G, Mantei N (1991) Rabbit small intestinal trehalase. Purification, cDNA cloning, expression, and verification of glycosylphosphatidylinositol anchoring. J Biol Chem 265: 15034–15039

    Google Scholar 

  • Shimada S, Kamada A, Asano S (1980) The cocoon trehalase of the silkworm, Bombyx mori. Insect Biochem 10: 49–52

    Google Scholar 

  • Shinbo H, Yaginuma T, Happ GM (1987) Purification and characterization of a prolin-rich secretory protein that is a precrusor to a structural protein of an insect spermatophore. J Biol Chem 262: 4794–4799

    Google Scholar 

  • Su H-Z, Sato Y, Yamashita O (1993) Purification, cDNA cloning and northern blot analysis of trehalase of pupal midgut of the silkworm, Bombyx mori Biochim Biophys Acta 1173: 217–224

    Google Scholar 

  • Su H-Z, Ikeda M, Sato Y, Saito H, Imai K, Isobe M, Yamashita O (1994) Molecular characterization of ovary trehalase of the silkworm, Bombyx mori, and its transcriptional activation by diapause hormone. Biochim Biophys Acta 1218: 366–374

    Google Scholar 

  • Sumida M, Yamashita O (1983) Purification and some properties of soluble trehalase from midgut of pharate adult of the silkworm, Bombyx mori. Insect Biochem 13: 257–265

    Google Scholar 

  • Takeda S, Kono Y, Mameda Y (1988) Induction of non-diapause eggs in Bombyx mori by a trehalase inhibitor. Entomol Exp Appl 46: 291–294

    Google Scholar 

  • Takesue Y, Yokota K, Nishi Y, Taguchi R, Ikezawa H (1986) Solubilization of trehalase from rabbit renal and intestinal brush-border membranes by phosphatidylinositol-specific phospholipase C. FEBS Lett 201: 5–8

    Google Scholar 

  • Takiguchi M, Niimi T, Su Z-H, Yaginuma T (1992) Trehalase from male accessory gland of an insect, Tenebrio molitor. cDNA sequencing and developmental profile of the gene expression. Biochem J 288: 19–22

    Google Scholar 

  • Talbot BG, Huber RE (1975) Partial purification, stabilization and characterization of adult honey bee midgut trehalase and a new trehalase specific disc gel stain method. Insect Biochem 5: 337–347

    Google Scholar 

  • Talbot BG, Muir JG, Huber RE (1975) Properties of a free and a solubilized form of bound α,α-trehalase purified from honey bee thorax. Can J Biochem 53: 1106–1117

    Google Scholar 

  • Terra WR, Ferreira C, Bastos F (1985) Phylogenetic considerations of insect digestion. Disaccharides and the spatial organization of digestion in Tenebrio molitor larvae. Insect Biochem 15: 443–449

    Google Scholar 

  • Terra WR, Ferreira C, Bianchi AG de (1978) Physical properties and tris inhibition of an insect trehalase and thermodynamic approach to the nature of its active site. Biochim Biophys Acta 524: 131–141

    Google Scholar 

  • Vaandrager SH, Haller TB, Marrewijk WJA van, Beenakkers AM Th (1989) Fractionation and kinetic properties of trehalase from flight muscles and haemolymph of the locust, Locusta migratoria. Insect Biochem 19: 84–89

    Google Scholar 

  • Valaitis AP, Bowers DF (1993) Purification and properties of the soluble midgut trehalase from the gypsy moth, Lymantria dispar. Insect Biochem Molec Biol 23: 599–606

    Google Scholar 

  • Wyatt GR (1967) The biochemistry of sugars and polysaccharides in insects. Adv Insect Physiol 4: 287–360

    Google Scholar 

  • Yaginuma T, Happ GM (1988) Trehalase from the bean-shaped accessory glands and the spermatophore of the male mealworm beetle, Tenebrio molitor. J Comp Physiol B 157: 765–770

    Google Scholar 

  • Yaginuma T, Happ GM (1989) 20-Hydroxyecdysone acts in the male pupa to commit accessory glands toward trehalase production in the adult mealworm beetle (Tenebrio molitor) Gen Comp Endocrinol 73: 173–185

    Google Scholar 

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Communicated by L.C.-H. Wang

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Yaginuma, T., Mizuno, T., Mizuno, C. et al. Trehalase in the spermatophore from the bean-shaped accessory gland of the male mealworm beetle, Tenebrio molitor: purification, kinetic properties and localization of the enzyme. J Comp Physiol B 166, 1–10 (1996). https://doi.org/10.1007/BF00264633

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