2014
DOI: 10.1016/j.bbapap.2013.12.021
|View full text |Cite
|
Sign up to set email alerts
|

FAD binding properties of a cytosolic version of Escherichia coli NADH dehydrogenase-2

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
7
0

Year Published

2014
2014
2016
2016

Publication Types

Select...
5

Relationship

4
1

Authors

Journals

citations
Cited by 12 publications
(8 citation statements)
references
References 53 publications
1
7
0
Order By: Relevance
“…Steady‐state and time‐resolved techniques used in this work were fully described in previous reports …”
Section: Methodsmentioning
confidence: 99%
“…Steady‐state and time‐resolved techniques used in this work were fully described in previous reports …”
Section: Methodsmentioning
confidence: 99%
“…In addition, the excitation beam was attenuated with a neutral density filter with approximately 20 % of transmittance to avoid photochemical processes during acquisition. The intrinsic and cofactor fluorescence quantum yields ( Φ F ) of the enzymes in air‐saturated buffer solutions were determined by comparison of the integrated fluorescence intensity using the emission spectra of authentic solutions of Trp (${\Phi _{\rm{F}}^{{\rm{Trp}}} }$ =0.14)12a and FAD (${\Phi _{\rm{F}}^{{\rm{FAD}}} }$ =0.028)38 in the same buffer as reference, with matched absorbance ( A ≈0.05) at the excitation wavelength to minimize internal filter effects. The steady‐state fluorescence anisotropy r of the samples was determined with a classical L ‐format and calculated as previously described 38…”
Section: Methodsmentioning
confidence: 99%
“…Since RB absorbs light both at the excitation and emission spectral regions of BSA, the observed emission spectra were corrected by the primary and secondary inner filter effects as described before [20,21].…”
Section: Steady-state Spectroscopic Measurementsmentioning
confidence: 99%
“…The fluorescence quantum yield (U F ) of RB in BSA solutions was determined by comparison of the integrated fluorescence intensity using as reference the emission of dye in buffer solution (U F = 0.018) [19]; keeping constant the absorbance value at the excitation wavelength (525 nm). Steadystate fluorescence anisotropy r of the RB was determined with a classical L-format and calculated as described elsewhere [20,21].…”
Section: Steady-state Spectroscopic Measurementsmentioning
confidence: 99%