RESUMO
The wild-type phototropin protein phot from the green alga Chlamydomonas reinhardtii with the blue-light photoreceptor domains LOV1 and LOV2 has flavin mononucleotide (FMN) as cofactor. For the LOV1-His domain from phot of C. reinhardtii studied here, the FMN chromophore was replaced by roseoflavin monophosphate (8-dimethylamino-8-demethyl-FMN, RoFMN) during heterologous expression in a riboflavin auxotropic Escherichia coli strain. An absorption and emission spectroscopic characterisation of the cofactor exchanged-LOV1-His (RoLOV1) domain was carried out in aqueous pH 8 phosphate buffer. The fluorescence of RoLOV1 is quenched by photo-induced charge transfer at room temperature. The photo-cyclic dynamics of RoLOV1 was observed by blue-light induced hypochromic and bathochromic absorption changes which recover on a minute timescale in the dark. Photo-excited RoFMN is thought to cause reversible protein and cofactor structural changes. Prolonged intense blue-light exposure caused photo-degradation of RoFMN in RoLOV1 to fully reduced flavin and lumichrome derivatives. Photo-cycle schemes of RoLOV1 and LOV1 are presented, and the photo-degradation dynamics of RoLOV1 is discussed.
Assuntos
Chlamydomonas reinhardtii/metabolismo , Fototropinas/química , Absorção , Mononucleotídeo de Flavina/química , Flavinas/química , Concentração de Íons de Hidrogênio , Fotólise , Fototropinas/metabolismo , Estrutura Terciária de Proteína , Riboflavina/análogos & derivados , Riboflavina/química , Espectrometria de Fluorescência , TemperaturaRESUMO
The E149A mutant of the cryDASH member cryptochrome 3 (cry3) from Arabidopsis thaliana was characterized in vitro by optical absorption and emission spectroscopic studies. The mutant protein non-covalently binds the chromophore flavin adenine dinucleotide (FAD). In contrast to the wild-type protein it does not bind N5,N10-methenyl-5,6,7,8-tetrahydrofolate (MTHF). Thus, the photo-dynamics caused by FAD is accessible without the intervening coupling with MTHF. In dark adapted cry3-E149A, FAD is present in the oxidized form (FAD(ox)), semiquinone form (FADH(.)), and anionic hydroquinone form (FAD(red)H(-)). Blue-light photo-excitation of previously unexposed cry3-E149A transfers FAD(ox) to the anionic semiquinone form (FAD()(-)) with a quantum efficiency of about 2% and a back recovery time of about 10s (photocycle I). Prolonged photo-excitation leads to an irreversible protein re-conformation with structure modification of the U-shaped FAD and enabling proton transfer. Thus, a change in the photocycle dynamics occurs with photo-conversion of FAD(ox) to FADH(.), FADH(.) to FAD(red)H(-), and thermal back equilibration in the dark (photocycle II). The photocycle dynamics of cry3-E149A is compared with the photocycle behaviour of wild-type cry3 and other photo-sensory cryptochromes.
Assuntos
Proteínas de Arabidopsis/química , Arabidopsis/química , Criptocromos/química , Substituição de Aminoácidos , Proteínas de Arabidopsis/metabolismo , Criptocromos/metabolismo , Flavina-Adenina Dinucleotídeo/química , Flavina-Adenina Dinucleotídeo/metabolismo , Mutagênese Sítio-Dirigida , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Espectrometria de Fluorescência , Tetra-Hidrofolatos/química , Tetra-Hidrofolatos/metabolismoRESUMO
The wild-type BLUF protein Slr1694 from Synechocystis sp. PCC6803 (BLUF=blue-light sensor using FAD) has flavin adenosine dinucleotide (FAD) as natural cofactor. This light sensor causes positive phototaxis of the marine cyanobacterium. In this study the FAD cofactor of the wild-type Slr1694 was replaced by roseoflavin (RoF) and the roseoflavin derivatives RoFMN and RoFAD during heterologous expression in a riboflavin auxotrophic E. coli strain. An absorption and emission spectroscopic characterization of the cofactor-exchanged-Slr1694 (RoSlr) was carried out both under dark conditions and under illuminated conditions. The behaviour of RoF embedded in RoSlr in aqueous solution at pH 8 is compared with the behaviour of RoF in aqueous solution. The fluorescence of RoF and RoSlr is quenched by photo-induced twisted intra-molecular charge transfer at room temperature with stronger effect for RoF. The fluorescence quenching is diminished at liquid nitrogen temperature. Light exposure of RoSlr causes irreversible conversion of the protein embedded roseoflavins to 8-methylamino-flavins, 8-dimethylamino-lumichrome and 8-methylamino-lumichrome.
Assuntos
Proteínas de Bactérias/química , Synechocystis/química , Absorção , Concentração de Íons de Hidrogênio , Luz , Fotólise , Riboflavina/análogos & derivados , Riboflavina/química , Espectrometria de Fluorescência , Espectrofotometria UltravioletaRESUMO
The photo-excitation dynamics of the mutants LOV1-C57S and LOV2-C250S of the LOV-domains of the phototropin photoreceptor phot from the green alga Chlamydomonas reinhardtii is investigated by absorption and fluorescence studies. The LOV domains fused to a maltose binding protein (MBP) are expressed in Escherichia coli. The mutants were studied under aerobic conditions in aqueous solution at pH 8. Blue-light exposure reduced the fully oxidized flavin mononucleotide, FMN(ox), to FMN semiquinone, FMNH*, (quantum efficiency around 1%) which further reduced to FMN hydroquinone, FMN(red)H(2) or FMN(red)H(-) (quantum efficiency ca. 3 x 10(-5)). In the dark both reduced forms recovered back to the oxidized form on a minute timescale. Besides photoreduction, blue-light photo-excitation of the mutants resulted in photoproduct formation (efficiency in the 2 x 10(-4) - 10(-3) range). Photo-reaction schemes for the mutants are discussed.
Assuntos
Benzoquinonas/análise , Chlamydomonas reinhardtii/efeitos da radiação , Mononucleotídeo de Flavina/efeitos da radiação , Animais , Benzoquinonas/efeitos da radiação , Chlamydomonas reinhardtii/genética , Mononucleotídeo de Flavina/metabolismo , Mutação , OxirreduçãoRESUMO
The BLUF protein Slr1694 from the cyanobacterium Synechocystis sp. PCC6803 is characterized by absorption and emission spectroscopy. Slr1694 expressed from E. coli which non-covalently binds FAD, FMN, and riboflavin (called Slr1694(I)), and reconstituted Slr1694 which dominantly contains FAD (called Slr1694(II)) are investigated. The receptor conformation of Slr1694 (dark adapted form Slr1694(r)) is transformed to the putative signalling state (light adapted form Slr1694(s)) with red-shifted absorption and decreased fluorescence efficiency by blue-light excitation. In the dark at 22 degrees C, the signalling state recovers back to the initial receptor state with a time constants of about 14.2s for Slr1694(I) and 17s for Slr1694(II). Quantum yields of signalling state formation of approximately 0.63+/-0.07 for both Slr1694(I) and Slr1694(II) were determined by transient transmission measurements and intensity dependent steady-state transmission measurements. Extended blue-light excitation causes some bound flavin conversion to the hydroquinone form and some photo-degradation, both with low quantum efficiency. The flavin-hydroquinone re-oxidizes slowly back (time constant 5-9 min) to the initial flavoquinone form in the dark. A photo-cycle dynamics scheme is presented.
Assuntos
Proteínas de Bactérias/química , Transdução de Sinal Luminoso , Luz , Receptores de Superfície Celular/química , Análise Espectral , Synechocystis/química , Proteínas de Bactérias/efeitos da radiação , Cor , Conformação Proteica/efeitos da radiação , Receptores de Superfície Celular/efeitos da radiaçãoRESUMO
The blue light photoreceptor cryptochrome 3 (cry3) from Arabidopsis thaliana was characterized at room temperature in vitro in aqueous solution by optical absorption and emission spectroscopic studies. The protein non-covalently binds the chromophores flavin adenine dinucleotide (FAD) and N5,N10-methenyl-5,6,7,8-tetrahydrofolate (MTHF). In the dark-adapted state of cry3, the bound FAD is present in the oxidized form (FAD(ox), ca. 38.5%), in the semiquinone form (FADH., ca. 5%), and in the fully reduced neutral form (FAD(red)H2) or fully reduced anionic form (FAD(red)H-, ca. 55%). Some amount of FAD (ca. 1.5%) in the oxidized state remains unbound probably caused by chromophore release and/or denaturation. Förster-type energy transfer from MTHF to FAD(ox) is observed. Photo-excitation reversibly modifies the protein conformation causing a slight rise of the MTHF absorption strength and an increase of the MTHF fluorescence efficiency (efficient protein conformation photo-cycle). Additionally there occurs reversible reduction of bound FAD(ox) to FAD(red)H2 (or FAD(red)H-, FAD(ox) photo-cycle of moderate efficiency), reversible reduction of FADH. to FAD(red)H2 (or FAD(red)H-, FADH. photo-cycle of high efficiency), and modification of re-oxidable FAD(red)H2 (or FAD(red)H-) to permanent FAD(red)H2 (or FAD(red)H-) with low quantum efficiency. Photo-excitation of MTHF causes the reversible formation of a MTHF species (MTHF', MTHF photo-cycle, moderate quantum efficiency) with slow recovery to the initial dark state, and also the formation of an irreversible photoproduct (MTHF'').
Assuntos
Proteínas de Arabidopsis/análise , Arabidopsis/química , Desoxirribodipirimidina Fotoliase/análise , Flavina-Adenina Dinucleotídeo/metabolismo , Flavoproteínas/química , Ácido Fólico/análogos & derivados , Absorção , Proteínas de Arabidopsis/química , Proteínas de Arabidopsis/metabolismo , Criptocromos , Desoxirribodipirimidina Fotoliase/química , Desoxirribodipirimidina Fotoliase/metabolismo , Transporte de Elétrons , Transferência de Energia , Flavina-Adenina Dinucleotídeo/química , Ácido Fólico/química , Ácido Fólico/metabolismo , Quinonas/química , Quinonas/metabolismo , Espectrometria de Fluorescência/métodos , Temperatura , Fatores de TempoRESUMO
The BLUF protein BlrB from the non-sulphur anoxyphototrophic purple bacterium Rhodobacter sphaeroides is characterized by absorption and emission spectroscopy. BlrB expressed from E. coli binding FAD, FMN, and riboflavin (called BrlB(I)) and recombinant BlrB containing only FAD (called BlrB(II)) are investigated. The dark-adapted proteins exist in two different receptor conformations (receptor states) with different sub-nanosecond fluorescence lifetimes (BLUF(r,f) and BLUF(r,sl)). Some of the flavin-cofactor (ca. 8%) is unbound in thermodynamic equilibrium with the bound cofactor. The two receptor conformations are transformed to putative signalling states (BLUF(s,f) and BLUF(s,sl)) of decreased fluorescence efficiency and shortened fluorescence lifetime by blue-light excitation. In the dark at room temperature both signalling states recover back to the initial receptor states with a time constant of about 2s. Quantum yields of signalling state formation of about 90% for BlrB(II) and about 40% for BlrB(I) were determined by intensity dependent transmission measurements. Extended blue-light excitation causes unbound flavin degradation (formation of lumichrome and lumiflavin-derivatives) and bound cofactor conversion to the semiquinone form. The flavin-semiquinone further reduces and the reduced flavin re-oxidizes back in the dark. A photo-dynamics scheme is presented and relevant quantum efficiencies and time constants are determined.
Assuntos
Diester Fosfórico Hidrolases/química , Fotoquímica , Rhodobacter sphaeroides/química , Sítios de Ligação , Mononucleotídeo de Flavina/química , Mononucleotídeo de Flavina/metabolismo , Flavina-Adenina Dinucleotídeo/química , Flavina-Adenina Dinucleotídeo/metabolismo , Flavoproteínas/química , Flavoproteínas/metabolismo , Oxirredução , Diester Fosfórico Hidrolases/metabolismo , Células Fotorreceptoras/química , Células Fotorreceptoras/metabolismo , Células Fotorreceptoras/efeitos da radiação , Espectrofotometria , Fatores de TempoRESUMO
An absorption and emission spectroscopic characterisation of the combined wild-type LOV1-LOV2 domain string (abbreviated LOV1/2) of phot from the green alga Chlamydomonas reinhardtii is carried out at pH 8. A LOV1/2-MBP fusion protein (MBP=maltose binding protein) and LOV1/2 with a His-tag at the C-terminus (LOV1/2-His) expressed in an Escherichia coli strain are investigated. Blue-light photo-excitation generates a non-fluorescent intermediate photoproduct (flavin-C(4a)-cysteinyl adduct with absorption peak at 390 nm). The photo-cycle dynamics is studied by dark-state absorption and fluorescence measurement, by following the temporal absorption and emission changes under blue and violet light exposure, and by measuring the temporal absorption and fluorescence recovery after light exposure. The fluorescence quantum yield, phi(F), of the dark adapted samples is phi(F)(LOV1/2-His) approximately 0.15 and phi(F)(LOV1/2-MBP) approximately 0.17. A bi-exponential absorption recovery after light exposure with a fast (in the several 10-s range) and a slow component (in the near 10-min range) are resolved. The quantum yield of photo-adduct formation, phi(Ad), is extracted from excitation intensity dependent absorption measurements. It decreases somewhat with rising excitation intensity. The behaviour of the combined wildtype LOV1-LOV2 double domains is compared with the behaviour of the separate LOV1 and LOV2 domains.
Assuntos
Chlamydomonas reinhardtii/genética , Cisteína/análogos & derivados , Mononucleotídeo de Flavina/análogos & derivados , Flavoproteínas/química , Fotorreceptores Microbianos/química , Estrutura Terciária de Proteína , Indexação e Redação de Resumos , Animais , Proteínas de Transporte/química , Criptocromos , Cisteína/administração & dosagem , Cisteína/farmacocinética , Mononucleotídeo de Flavina/administração & dosagem , Mononucleotídeo de Flavina/química , Mononucleotídeo de Flavina/farmacocinética , Polarização de Fluorescência , Histidina/química , Proteínas Ligantes de Maltose , Proteínas Recombinantes de Fusão/química , Riboflavina/análogos & derivados , Espectrometria de Fluorescência , EspectrofotometriaRESUMO
The absorption and emission behavior of flavin mononucleotide (FMN) in the light-, oxygen- and voltage-sensitive (LOV) domain LOV1 of the photoreceptor Phot1 from the green alga Chlamydomonas reinhardtii was studied. The results from the wild-type (LOV1-WT) were compared with those from a mutant in which cysteine 57 was replaced by serine (LOV1-C57S), and with free FMN in aqueous solution. A fluorescence quantum yield of phi(F) = 0.30 and a fluorescence lifetime of tau(F) = 4.6 ns were determined for FMN in the mutant LOV1-C57S, whereas these quantities are reduced to about phi(F) = 0.17 and tau(F) = 2.9 ns for LOV1-WT, indicating an enhanced intersystem crossing in LOV1-WT because of the adjacent sulfur of C57. A single-exponential fluorescence decay was observed in picosecond laser time-resolved fluorescence measurements for both LOV1-WT and LOV1-C57S as expected for excited singlet state relaxation by intersystem crossing and internal conversion. An excitation intensity dependent fluorescence signal saturation was observed in steady-state fluorescence measurements for LOV1-WT, which is thought to be because of the formation of a long-lived intermediate flavin-C(4a)-cysteinyl adduct in the triplet state (few microseconds triplet lifetime, adduct lifetime around 150 s). No photobleaching was observed for LOV1-C57S, because no thiol group is present in the vicinity of FMN for an adduct formation.
Assuntos
Chlamydomonas reinhardtii/metabolismo , Mononucleotídeo de Flavina/química , Fosfoproteínas/química , Animais , Sítios de Ligação , Mononucleotídeo de Flavina/metabolismo , Cinética , Microscopia de Fluorescência , Estrutura Molecular , Fosfoproteínas/metabolismo , EspectrofotometriaRESUMO
The photo-fading of the S0-S1 absorption band of the infrared dye indocyanine green sodium iodide (ICG-NaI) has been studied by cw laser excitation to the S1 band. Monomeric solutions in water, heavy water, aqueous sodium azide, human plasma, methanol and dimethyl sulfoxide (DMSO) as well as J-aggregated solutions in H2O and D2O have been investigated. A leucoform of indocyanine green seems to be formed by photodegradation. The degradation slows down with exposure time. The initial degradation yield, phi D,0, is determined. In monomeric and dimeric water, heavy water and sodium azide solutions the initial photostability is of the order of phi D.0 approximately 10(-3), in the organic solvents methanol and DMSO it is of the order of phi D.0 approximately 10(-5), and in human plasma it is phi D.0 approximately 2 x 10(-6). J-aggregates at high concentration are very stable. The thermal stability of the ICG-NaI solutions at room temperature in the dark is compared with their photostability. The thermal degradation time of monomeric and dimeric ICG-NaI in water, heavy water and sodium azide solutions is t(th) approximately 10 days, while no thermal degradation is observed for ICG-NaI J-aggregates and ICG-NaI in methanol, DMSO and human plasma.
Assuntos
Corantes/análise , Verde de Indocianina/análise , Calefação , Humanos , Lasers , Estrutura MolecularRESUMO
Femtosecond pulses of a passive mode-locked Rhodamine-6G dye laser are amplified in a double-stage, three-pass, plane mirror, Sulforhodamine-101 amplifier system. Saturable filters (Schott glass RG645 and Malachite Green) are used to suppress amplified spontaneous emission. Input pulses of 110-fs duration are broadened to 240 fs in the amplifier system and recompressed to 75 fs in a prism-pair compressor. Using a 20-Hz Q-switched Nd:YAG pump laser of 50-mJ second-harmonic output energy, we obtained amplified and recompressed pulses of 180-µJ energy at 625 nm starting with 40-pJ input pulses. The small-signal amplification dynamics is studied numerically. Relevant gain dye and saturable filter parameters are derived. The influence of amplified spontaneous emission is analyzed.
RESUMO
The principal optical constants n(o), k(o), n(e), and k(e) of the hexagonal crystal CdSe are determined in the wavelength region between 380 and 950 nm at room temperature. The minimum reflectivities and the corresponding Brewster angles of parallel polarized light are measured for ordinary and extraordinary rays in the wavelength region between 380 and 728 nm. At longer wavelengths (k(o) < 10(-3)) Brewsterangle measurements and transmission measurements were applied. A plot of the absorption coefficients alpha(o) and alpha(e) versus wavelength indicates deviations from a direct band-gap parabolic absorption dependence.
RESUMO
This special issue of Applied Optics provides a perspective on recent trends in dye laser research.
RESUMO
The influence of self-phase modulation (SPM) and group-velocity dispersion (GVD) on pulse development in a passive mode-locked dye laser is investigated numerically by using fast Fourier transformations. The situation of positive SPM is considered. Four regions of laser performance may be distinguished: (i) In the positive GVD region pulse broadening by GVD must be balanced by the pulse-shortening effect of the saturable absorber. (ii) In a region around zero GVD the laser is periodically self-quenching and the temporal and spectral pulse shapes change periodically similar to higher-order solitons. (iii) It follows a negative GVD region where stable pulses of smooth temporal and spectral shapes are generated similar to fundamental solitons. In this region the pulse duration is practically independent of the saturable absorber concentration, and the saturable absorber is needed mainly for background suppression. (iv) Further increasing the negative GVD, pulse broadening must be balanced by the saturable absor ber pulse shortening.