Journal of Physical Chemistry A: Molecules, Spectroscopy, Kinetics, Environment and General Theory 2012-07-19

Comparative study of the photoprotolytic reactions of D-luciferin and oxyluciferin.

Yuval Erez, Itay Presiado, Rinat Gepshtein, Luís Pinto da Silva, Joaquim C G Esteves da Silva, Dan Huppert

文献索引:J. Phys. Chem. A 116 , 7452-7461, (2012)

全文:HTML全文

摘要

Optical steady-state and time-resolved spectroscopic methods were used to study the photoprotolytic reaction of oxyluciferin, the active bioluminescence chromophore of the firefly's luciferase-catalyzed reaction. We found that like D-luciferin, the substrate of the firefly bioluminescence reaction, oxyluciferin is a photoacid with pK(a)* value of ∼0.5, whereas the excited-state proton transfer (ESPT) rate coefficient is 2.2 × 10(10) s(-1), which is somewhat slower than that of D-luciferin. The kinetic isotope effect (KIE) on the fluorescence decay of oxyluciferin is 2.5 ± 0.1, the same value as that of D-luciferin. Both chromophores undergo fluorescence quenching in solutions with a pH value below 3.


相关化合物

  • D-虫荧光素钾盐

相关文献:

Brazilin Isolated from Caesalpinia sappan suppresses nuclear envelope reassembly by inhibiting barrier-to-autointegration factor phosphorylation.

2015-08-01

[J. Pharmacol. Exp. Ther. 352(1) , 175-84, (2014)]

Label-free phenotypic profiling identified D-luciferin as a GPR35 agonist.

2012-01-01

[PLoS ONE 7 , e34934, (2012)]

Affordable luciferase reporter assay for cell-based high-throughput screening.

2013-04-01

[J. Biomol. Screen. , (2012)]

Bioluminescent imaging of Trypanosoma cruzi infection in Rhodnius prolixus.

2012-01-01

[Parasit. Vectors 5 , 214, (2012)]

Influence of bioluminescence imaging dynamics by D-luciferin uptake and efflux mechanisms.

2012-01-01

[Mol. Imaging 11 , 499-506, (2012)]

更多文献...