2007
DOI: 10.1007/s00792-007-0099-5
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Roles of a short connecting disulfide bond in the stability and function of psychrophilic Shewanella violacea cytochrome c 5*

Abstract: Cys-59 and Cys-62, forming a disulfide bond in the four-residue loop of Shewanella violacea cytochrome c (5) (SV cytc (5)), contribute to protein stability but not to redox function. These Cys residues were substituted with Ala in SV cytc (5), and the structural and functional properties of the resulting C59A/C62A variant were determined and compared with those of the wild-type. The variant had similar features to those of the wild-type in absorption, circular dichroic, and paramagnetic (1)H NMR spectra. In ad… Show more

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Cited by 24 publications
(27 citation statements)
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“…19) It is likely that the somewhat conserved environment of mitochondria in eukaryotic cells can maintain the conserved cyt c interior around the heme. For further examples in an expanded range of growth temperatures, we are currently examining class IE cyts c isolated from mesophilic Shewanella amazonensis and psychrophilic Shewanella violacea, 20) which grow optimally at 35 and 8 C respectively.…”
Section: Discussionmentioning
confidence: 99%
“…19) It is likely that the somewhat conserved environment of mitochondria in eukaryotic cells can maintain the conserved cyt c interior around the heme. For further examples in an expanded range of growth temperatures, we are currently examining class IE cyts c isolated from mesophilic Shewanella amazonensis and psychrophilic Shewanella violacea, 20) which grow optimally at 35 and 8 C respectively.…”
Section: Discussionmentioning
confidence: 99%
“…Many y To whom correspondence should be addressed. Fax: +81-3-5317-9433; E-mail: htamegai@chs.nihon-u.ac.jp studies have been carried out on the respiratory system of S. violacea and on related strains for comparison, [19][20][21][22] but it remains unknown whether this phenomenon observed in S. violacea is universal to piezophiles.…”
Section: )mentioning
confidence: 99%
“…Thermal denaturation experiments were carried out by monitoring CD spectra in a pressure-proof cell compartment (JASCO) that was attached to a JASCO J-820 CD spectrometer. 14) Protein solutions of the air-oxidized holo AA c 555 and holo and apo C12A/C15A variants (20 mM) in 20 mM sodium acetate (pH 5.0) were subjected to analysis. The temperature-dependent CD ellipticity change at 222 nm was monitored in a cuvette of 1 mm pathlength.…”
Section: )mentioning
confidence: 99%