5th International symposium on bioluminescence and chemiluminescence

5th International symposium on bioluminescence and chemiluminescence

trendsinanalyticalchemistry,vol.8, no. 2,1989 appear from other symposiathat the quality of the science involved may be inverselyproportional to the ...

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trendsinanalyticalchemistry,vol.8, no. 2,1989

appear from other symposiathat the quality of the science involved may be inverselyproportional to the number of papers presented. The Zlatkis Symposia have shown an optimum balance between scientific quality and the size of the program. It is

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hoped that the Minnesota Chromatography Discussion Group will maintain this balance. R. P. W. SCOTT Dr. R. P. W. Scott’s address is 2 Sprucewood Lane, Aron, CT 06001, U.S.A.

Fundamentals and applications of bioluminescence and chemiluminesckce

A report of the Fifth International Symposium on Bioluminescence

These occasional meetings, held at two to three year intervals, embrace both the applications and fundamentals of the subject. Previous symposia were held in Brussels, Belgium (1978), San Diego, U.S.A. (1981), Birmingham, U.K. (1984), and Freiburg, F.R.G. (1986). The next one is scheduled for June 1990 at Harvard. Around 350 delegates registered for the Symposium which commenced in Florence at the Palazzo dei Congressi on Sunday evening with the DeLuca Memorial Lecture given by Professor Hastings, who discussed the biochemistry and circadian control of the bioluminescent dinoflagellate Gonyaulux. The Marlene DeLuca price (donated by Laboratorium Prof. Dr. Berthold, Wildbad, F.R.G.) for the best abstract submitted by a young worker, was shared by Dr. Reiber of the University of Gottingen (luminescence of brain cell preparations) and Dr. Hauber from the University of Munich (protein blotting and nucleic hybridisation detected using firefly luciferase and luciferyl-O-phosphate). There were around eighty invited and contributed papers and about a hundred posters. Concurrent sessions were held and the programme included half day workshops on three commercially available luminescence immunoassays. On Tuesday the symposium programme moved to Bologna with del-

egates travelling by special train. The University of Bologna is this year celebrating its Ninth Century Anniversary as the oldest university in the world and the occasion was also marked by the conferring of an Honorary Doctorate on Professor McElroy in recognition of his outstanding achievements in forty years of work on bioluminescence, particularly on the firefly system. Two lectures were presented in which reminiscences were given of working in McElroy’s team in earlier days. Seliger recounted field work in Jamaica and Hastings the early days at John Hopkins University. As a contrast to work done three decades ago a further two lectures were presented showing very modern aspects of bioluminescence. Baldwin spoke about lux genes in Photobacterium and Wood discussed his recent work done in the McElroy and DeLuca laboratory on site directed mutagenesis of the luciferases from the click beetle (Pyrophorus) with some excellent illustrations showing the various colours of light that may be produced . The symposium opened on Monday with a sesssion on firefly bioluminescence. The first two lectures covered the fundamental biochemistry and addressed aspects of genetic engineering and luciferase enzyme light kinetics. These were followed by three others on the application of ATP assays, particularly in rapid microbiology, and the do’s and don’ts of the technique. Sensitivities for ATP in the subfemtomole range are now rather easily accessible. Photoemission from living organisms and our understanding of the chemistry

and physics of the underlying processeswas the topic the next session. Of particular interest was the paper by Khan on singlet oxygen spectroscopy in biological reactions. Luminescence immunoassay formed a major portion of the symposium with papers from Ekins, Woodhead and Yegorov amongst some twenty contributions. It was clear from these papers and the posters that exciting advances have been made since the last meeting two years ago with new labels and new end-point species being introduced. Further, new luminescent enzyme substrates for use with enzymes such as alkaline phosphatase were described and which allow sensitivities for analytes in the attomole range. A new session for these symposia covered luminescence-based biosensors with immunosensors and luminescent reagents and luciferases immobilised onto transparent materials which are then viewed directly by a photomultiplier or via an optical fibre. Such electrodes may be used upwards of fifty times for some formats. Luminescent Escherichia coli was also described as a sensor for biologically active compounds Chemiluminescence and bioluminescence-based applications were covered by a range of lectures and posters, and included clinical applications for platelets and hormones together with a substantial number of contributions concerning genetic engineering (lux genes, reporter genes etc.) and chemiluminescent-based detection for DNA hybridisation and probes. Bacterial luciferase to assay NAD(P)H and compounds conjugate with it (such as bile acids and dehydrogenases as well as immobilised luciferases and peroxidases) were also reported. There was also a review by Campbell on the use of photoproteins in measuring ionic calcium in cells and other situations. New reagents for post-column detection of compounds eluted from high-performance liquid chromatography columns by chemiluminescence were also featured. A substantial number of contributions covered luminescence from phagocytosis including clinical applications and fundamentals with dis-

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trendsinanalyticalchemistry,vol.8, no. 2,1989

cussion of the oxygen chemistry involved in this process. The use of microtitre plate luminometers to appraise up to ninety-six samples at a time was reported by two groups of workers. The contributions in the phagocytosis and allied areas were very diverse and justice cannot be done to them in this short review. Interested readers should consult the abstracts which are now available (see below). Photon imaging was also covered and one contributor (Scott) showed a very impressive video-film in timelapse mode of light being emitted

from germinating seeds. The use of a

uted papers will be published as a

charge coupled device (CCD), usually used by astronomers, was reported for the ultrasensitive detection of afetoprotein and other clinically relevant compounds. The possibilities of imaging by such instruments opens up a new dimension in cellular investigations as well as for the detection of luminescent areas on chromatograms, electrophoretograms, microtitre plates and similar. The symposium abstracts have been published in the Journal of Bioluminescence and Chemiluminescence (Vol. 2, No. 4). The contrib-

special supplement to the Journal and the posters will appear as short papers in forthcoming regular issues of the same. Professor Pazzagli (University of Florence) and Professor Roda (University of Bologna) and their teams are to be congratulated upon an extremely well run and successful symposium. PHILIP E . STANLEY Philip E. Stanley is a Consultant Scientist, 48 Glisson Road, Cambridge, CBI 2HF, U.K.

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