The roles of the two highly unstable components F and P involved in the bioluminescence of euphausiid shrimps

Bioluminescence of euphausiids takes place when a fluorescent tetrapyrrole F and a highly unstable protein P react in the presence of oxygen. A previous study on the euphausiid Meganyctiphanes norvegica indicated that F acts as a catalyst and P is consumed in the luminescence reaction, differing from the luminescence system of dinoflagellates in which a tetrapyrrole luciferin, nearly identical to F, is enzymatically oxidized in the presence of dinoflagellate luciferase. In the present study, P was extracted from Euphausia pacifica as well as from M. norvegica, then purified separately by affinity chromatography on a column of biliverdin–Sepharose 4B, completing the whole process in less than 5h. The samples of P obtained from both species had a molecular weight of 600,000, a purity of about 80%, and a specific activity 50–100 times greater than that previously found. The activity of P rapidly decreased in solutions, even at 0°C, and the inactivation of P derived from M. norvegica was more than four times faster than that derived from E. pacifica. The kinetics of the luminescence reaction was investigated with F and P whose concentrations were systematically varied. The reaction was characteristically slow and involved two different reaction rates; the turnover number at 0°C was 30/h for the initial 20 min and 20/h after the initial 1 h. The total light emitted in a 50-h period indicated that the bioluminescence quantum yield of F was about 0.6 at 0°C, and P recycled many times in the luminescence reaction. Thus, the present results conclusively show that F is a luciferin and P is a luciferase of an unusually slow-working type, contrary to early report.     

The gastric mill of euphausiid crustaceans: a comparison of eleven species

The morphology of the gastric mill of 11 species in the family Euphausiidae is described. Two distinct arrangements can be recognized with respect to presence or absence of lateral teeth. One is the well-developed gastric mill of Thsanoessa gregaria, T. inermis, T. macrura and Pseudeuphausia sinica; the other is the gastric mill without lateral teeth of Nematoscelis atlantica, N. difficilis, N. megalops, Nematobrachion flexipes, N. sexspinosum, Stylocheiron abbreviatum, and S. carinatum. This supports the close relationships of the four species of both genera, Thysanoessa and Pseudeuphausia on the one hand and seven species belonging to Nematobrachion, Nematoscelis, and Stylocheiron on the other hand. The hypothesis that species in the same genus have similar gastric mill morphology, which was once rejected in the genus Thysanopoda, is accepted in all five genera examined here. Functional morphology of euphausiid foreguts is discussed.