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Presence of coelenterazine in mesopelagic fishes from the Strait of Messina

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Abstract

Coelenterazine, a luciferine, and luciferase activity specific to coelenterazine were detected and assayed in various tissues of mid-water fishes, Argyropelecus hemigymnus, Chauliodus sloani, Myctophum punctatum, Vinciguerria attenuata and Cyclothone braueri. Coelenterazine was found mainly in digestive systems and photophores of these fishes. A large species to species variation was found: extremely high levels of coelenterazine and luciferase were found in the M. punctatum digestive system whereas only a very low level of coelenterazine was detected in C. braueri. Coelenterazine was detected in A. hemigymnus eggs supporting the hypothesis of a maternal transfer of luminous capabilities. Luciferase activity specific to coelenterazine was found in photophores as well as in various other tissues suggesting another (besides light emission) biological function for this enzymatic activity. Distribution of coelenterazine in all tissues of the individuals supports the hypothesis of the dietary acquisition of coelenterazine by these fishes.

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References

  • Baguet F, Marechal G (1976) Bioluminescence of bathypelagic fish from the Strait of Messina. Comp Biochem Physiol 53C: 75–82

    Google Scholar 

  • Baguet F, Marechal G (1978) The stimulation of isolated photophores (Argyropelecus) by epinephrine and norepinephrine. Comp Biochem Physiol 60C: 137–143

    Google Scholar 

  • Campbell AK (1988) Bioluminescence: living light. Chap. 3. In: Chemiluminescence. Principles and applications in biology and medicine. Ellis Horwood Ltd., Chichester and, VCH Verlagsgesellschaft mbh, Weinheim, pp 127–239

    Google Scholar 

  • Campbell AK, Herring PJ (1990) Imidazolopyrazine bioluminescence in copepods and other marine organisms. Mar Biol 104: 219–225

    Google Scholar 

  • Cormier MJ (1978) Comparative biochemistry of animal systems. In: Herring PJ (ed). Bioluminescence in action. Academic Press, London, pp 75–108

    Google Scholar 

  • Denton EJ, Herring PJ, Widder EA, Latz MF, Case JF (1985) The roles of filters in photophores of oceanic animals and their relations to vision in the oceanic environment. Proc R Soc Lond 225: 63–97

    Google Scholar 

  • Dunlap JC, Hastings JW, Shimomura O (1980) Cross-reactivity between the light emitting systems of distantly related organisms: novel type of light-emitting compound. Proc natn Acad Sci USA 77: 1394–1397

    Google Scholar 

  • Foran D (1991) Evidence of luminous bacterial symbionts in the light organs of myctophids and stomiiform fishes. J exp Zool 259: 1–8

    Google Scholar 

  • Hastings JW (1983) Biological diversity, chemical mechanisms and the evolutionary origins of bioluminiscent systems. J molec Evolut 19: 309–321

    Google Scholar 

  • Hastings JW, Morin G (1991) Bioluminescence. Chap. 3. In: Prosser CL (ed) Neural and integrative animal physiology. Comparative animal physiology. 4th edn. John Wiley and Sons, New York, Chichester, pp 131–170

    Google Scholar 

  • Haygood M, Mowlds G, Rosenblatt R (1993) Do photophores of myctophid and stomiiform fishes contain bacterial symbionts? Proc Bioluminescence Symp 9: p 55

    Google Scholar 

  • Haygood M, Mowlds G, Rosenblatt R (1994) Bioluminescence of mictophid and stomiiform fishes is not due to bacterial luciferase. J exp Zool 270 (2): 225–231

    Google Scholar 

  • Herring PJ (1983) The spectral characteristics of luminous marine organisms. Proc R Soc Lond 220: 183–217

    Google Scholar 

  • Hopkins TL, Baird RC (1975) Net feeding in mesopelagic fishes. Fish Bull US 73: 908–914

    Google Scholar 

  • Inoue S, Kakoi H, Goto T (1976) Squid bioluminescence. III. Isilation and structure of Watasenia luciferin. Tetrahedron Lett 34: 2971–2974

    Google Scholar 

  • Inoue S, Kakoi H, Okada K, Goto T (1979) Fish bioluminescence. II. Trace characterization of the luminescent systems of a Myctophina fish, Diaphus elucens. Chemy Lett 1979: 253–256

    Google Scholar 

  • Inoue S, Okada K, Kakoi H, Goto T (1977) Fish bioluminescence. I. Isolation of luminescent substance from a Myctophina fish, Neoscopelus microchir and identification of it as Oplophorus luciferin. Chemy Lett 1977: 257–258

    Google Scholar 

  • Kinzer J, Shulz K (1988) Vertical distribution and feeding patterns of midwater fish in the central equatorial Altantic. II. Sternoptychidae. Mar Biol 99: 261–269

    Google Scholar 

  • Mallefet J, Baguet F (1985) Effects of adrenalin on the oxygen consumption and luminescence of the photophores of the mesopelagic fish Argyropelecus hemigymnus. J exp Biol 118: 341–349

    Google Scholar 

  • Merrett NR, Roe HSJ (1974) Patterns and selectivity in the feeding of certain mesopelagic fishes. Mar Biol 28: 115–126

    Google Scholar 

  • Morin JG, Hastings JW (1971) Biochemistry of the bioluminescence of colonial hydroids and other coelenterates. J cell Physiol 77: 305–311

    Google Scholar 

  • Rees JF, Thompson EM, Baguet F, Tsuji FI (1990) Detection of coelenterazine and related luciferase activity in the tissues of the luminous fish, Vinciguerria attenuata. Comp Biochem Physiol 96A: 425–430

    Google Scholar 

  • Rees JF, Thompson EM, Baguet F, Tsuji FI (1992) Evidence for the utilization of coelenterazine as the luminescent substrate in Argyropelecus photophores. Molec mar Biol Biotechnol 1 (3): 219–225

    Google Scholar 

  • Shimomura O (1987) Presence of coelenterazine in non-bioluminescent marine organisms. Comp Biochem Physiol 86B: 361–363

    Google Scholar 

  • Shimomura O, Inoue S, Johnson FH, Haneda Y (1980) Widespread occurrence of coelenterazine in marine bioluminescence. Comp Biochem Physiol 65B: 435–437

    Google Scholar 

  • Shimomura O, Johnson FH (1975) Regeneration of the photoprotein aequorin Nature, Lond 256: 236–238

    Google Scholar 

  • Shimomura O, Masugi T, Johnson FH, Haneda Y (1978) Properties and reaction mechanisms of the bioluminescent system of the deep-sea shrimp Oplophorus gracilorostris. Biochemistry, NY 17: 994–998

    Google Scholar 

  • Thompson EM, Nafpaktitis BG, Tsuji FI (1987) Induction of bioluminescence of the marine fish Porichthys by Vargula (crustacean) luciferin. Evidence for de novo synthesis or recycling of luciferin. Photochem Photobiol 45: 529–533

    Google Scholar 

  • Thompson EM, Toya Y, Nafpaktitis BG, Goto T, Tsuji FI (1988) Induction of bioluminescence capability in the marine fish Porichthys notatus by Vargula (crutacean) (14C) luciferin and unlabelled analogues. J exp Biol 137: 39–51

    Google Scholar 

  • Tsuji FI, Haneda Y (1971) Luminescent system in a myctophid fish Diaphus elucens Brauer. Nature, Lond 233: 623–624

    Google Scholar 

  • Tsuji FI, Haneda Y, Lynch RV III, Sugiyama N (1971) Luminescence cross-reactions of Porichthys luciferin and theories on the origin of luciferin in some shallow-water fishes. Comp Biochem Physiol 40A: 163–179

    Google Scholar 

  • Young RE, Roper CFE, Mangold K, Leisman G, Hochberg FG (1979) Luminescence from non-bioluminescent tissues in oceanic cephalopods. Mar Biol 53: 69–77

    Google Scholar 

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Communicated by O. Kinne, Oldenburg/Luhe

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Mallefet, J., Shimomura, O. Presence of coelenterazine in mesopelagic fishes from the Strait of Messina. Marine Biology 124, 381–385 (1995). https://doi.org/10.1007/BF00363911

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  • DOI: https://doi.org/10.1007/BF00363911

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