Luminescent emissions

The protein contains an N-terminal signal peptide of 17 amino acid residues for secretion. The luminescence reaction of coelenterazine catalyzed by the recombinant luciferase shows a luminescence emission maximum at 485 nm, whereas the luminescence catalyzed by the native luciferase shows a maximum at 480 nm. 

According to the Kuwabara-Wassink paper, the purified luciferin in aqueous neutral buffer solution showed an absorption maximum at 320 nm, and a fluorescence emission peak at 490 nm. The luminescence emission maximum measured with Airth s fungal luciferase system was 524 nm at pH 6.5, whereas the chemiluminescence emission maximum of the luciferin with H2O2 plus a droplet of strong NaOH plus ferrous sulfate was 542 nm. No information was reported on the chemical nature of the luciferin. 

Luminescence of Pyrosoma. All species of the genus Pyrosoma (about 10 species) are bioluminescent. Pyrosoma is one of the few organisms reported to luminesce in response to light (Bowlby et al., 1990). The luminescence emission spectrum of Pyrosoma atlantica is bimodal according to Kampa and Boden (1957), with the primary peak near 482 nm, and the secondary near 525 nm. Swift et al. (1977) reported the emission maxima of two Pyrosoma species at 485 and 493 nm, respectively, and Bowlby et al. (1990) found an emission peak at 475 nm with P. atlantica. A corrected bioluminescence spectrum of P. atlantica (A.max 485 nm) reported by Herring (1983) is shown in Fig. 10.5.2. 

Em., luminescence emission Q, quantum yield of coelenterazine (unpublished data included). Recombinant protein. 

More fluorescence features than just the emission intensity can be used to develop luminescent optosensors with enhanced selectivity and longer operational lifetime. The wavelength dependence of the luminescence (emission spectmm) and of the luminophore absorption (excitation spectrum) is a source of specificity. For instance, the excitation-emission matrix has shown to be a powerful tool to analyze complex mixtures of fluorescent species and fiber-optic devices for in-situ measurements (e.g. 

An ingenious variation on the standard fluorescence methods was proposed by Red kin et al. [50]. Water samples were extracted with non-polar solvents, transferred into hexane and the hexane solution frozen at 77 K. At that temperature the normally diffuse luminescence emission bands are present as sharp emission lines, making identification of fluorescing compounds considerably simpler. In the case of a complex mixture, some separation by column or thin layer chromatography might be necessary. 

The first example of luminescence emission from solids, of which written documents exist, date from the Italian Renaissance, originating from the accidental discovery around the year 1600 (1602 or 1603) by a Bolonian shoemaker and alchemist, called Vincencio Casciarolo or Casciarolus. He melted heavy bricks, close to his house, hoping to extract precious metals from them. 

B. Thermo luminescence Emission from solids and crystals on mild heating... 

Obelin is a Ca2+-activated bioluminescent photoprotein that has been isolated from the marine polyp Obelia longissima. Binding of calcium ions determines a luminescent emission. The protein consists of 195 amino acid residues [264] and is composed of apoobelin, coelenterazine, and oxygen. As aequorin, it contains three EF-hand Ca2+-binding sites and the luminescent reaction may be the result of coelenterazine oxidation by way of an intramolecular reaction that produces coelenteramide, C02, and blue light. As for aequorin, the luminescent reaction of obelin is sensitive to calcium and the protein was used in the past as an intracellular Ca2+ indicator. More recently, the cloning of cDNA for apoobelin led to the use of recombinant obelin as a label in different analytical systems. 

With the newly proposed detector, Dadoo et al. [84] adapted this bioluminescence reaction to determine ATP. A selective and sensitive determination is achieved because the use of CE as a separation technique minimizes the effect of several interfering substances such as some anions (e.g., SCN, I ) that inhibit the reaction decreasing the luminescence emission, and even some nucleotides that generate light in this reaction but with lower intensity. A detection limit of 5 nM, approximately 3 orders of magnitude lower than using UV detection, was obtained. 

The much larger energy difference between Si and S0 than between any successive excited states means that, generally speaking, internal conversion between Si and S0 occurs more slowly than that between excited states. Therefore, irrespective of which upper excited state is initially produced by photon absorption, rapid internal conversion and vibrational relaxation processes mean that the excited-state molecule quickly relaxes to the Si(v0) state from which fluorescence and intersystem crossing compete effectively with internal conversion from Si. This is the basis of Kasha s rule, which states that because of the very rapid rate of deactivation to the lowest vibrational level of Si (or Td, luminescence emission and chemical reaction by excited molecules will always originate from the lowest vibrational level of Si or T ... 

The fluorescence lifetime of the /2 metastable state of Nd + ions in LaBGeOs (a solid state laser) is 280 /u.s and its quantum efficiency is 0.9. (a) Calculate the radiative and nonradiative rates from this excited state, (b) If the effective phonons responsible for the nonradiative rate have an energy of 1100 cm, use the Dieke diagram to determine the number of emitted effective phonons from the F3/2 excited state, (c) From which three excited states of the Nd + ions in LaBGeOs do you expect the most intense luminescence emissions to be generated ... 

However, luminescence lifetime, which is a measure of the transition prob-abihty from the emitting level, may be effectively used. It is a characteristic and unique property and it is highly improbable that two different luminescence emissions will have exactly the same decay time. The best way to determine a combination of the spectral and temporal nature of the emission is by using laser-induced time-resolved spectra. The time-resolved technique requires relatively complex and expensive instrumentation, but its scientific... 

Stimulated release from an electron from the trap to the collection band, followed by emissive recombination with an activator. This process is called thermoluminescence (electron release stimulated by heating) and optically stimulated luminescence (electron release stimulated by light) (Fig. 2.6d) Extrinsic luminescence, where after being excited, electrons of defect ions recombine with the ground state with luminescence emission (Fig. 2.6e) ... 

Another possible solution that has been under development for three decades is to use a pulsed laser and time-resolved detection to allow the Raman photons to be discriminated from the broad luminescence background. The Raman interaction time is virtually instantaneous (less than 1 picosecond), whereas luminescence emission is statistically relatively slow, with minimum hundreds of picoseconds elapsing between electronic excitation and radiative decay. If we illuminate a sample with a very short (= 1 ps) laser pulse, all of the Raman... 

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