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  • Canadian Science Publishing  (3)
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  • Canadian Science Publishing  (3)
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  • 1
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1986
    In:  Biochemistry and Cell Biology Vol. 64, No. 4 ( 1986-04-01), p. 328-336
    In: Biochemistry and Cell Biology, Canadian Science Publishing, Vol. 64, No. 4 ( 1986-04-01), p. 328-336
    Abstract: The washed cells of Rhodopseudomonas sphaeroides f.sp. denitrificans developed a Δp of about −175 to −200 mV during denitrification in the dark and −200 to −245 mV in the light. With NO 2 − as the terminal acceptor, Δp was less than with NO 3 − , N 2 O, or O 2 . The values of Δψ in the dark were about −150 mV for NO 3 − and N 2 O and −140 mV for NO 2 − . During photodenitrification with NO 3 − , NO 2 − , or N 2 O or respiration to O 2 in light, Δψ ranged between −152 and −167 mV. Like Δψ, the ΔpH was higher in light than in the dark, resulting in a 20- to 30-mV increase in Δp during illumination with NO 3 − , NO 2 − , or N 2 O as the acceptor. Both ΔpH and Δψ were reduced at higher pH values (≥ 7.5). Changes in pH in response to O 2 in the light were less than those in the dark, indicating light inhibition of O 2 respiration. The cells maintained a reasonably high Δp without addition of a substrate or when inhibitors were used; the cells retained a fairly high Δψ even in the presence of an inhibitor. However, ΔpH was appreciably lowered and in some cases it was almost abolished when either KCN, rotenone, NaN 3 , carbonyl cyanide m-chlorophenylhydrazone (CCCP), 2,4-dinitrophenol, N,N′-dicyclohexylcarbodiimide, antimycin A, or 2-n-heptyl-4-hydroxyquinoline-N-oxide (HOQNO) was used. The combination of an uncoupler (e.g., CCCP) and an electron transport effector (e.g., antimycin A) further reduced the ΔpH. Antimycin A and HOQNO were more effective in inhibiting photosynthetic electron transport to NO 3 − , NO 2 − , N 2 O, or O 2 than the dark respiration to these substrates. Dibromomethylisopropyl-p-benzoquinone, a quinone antagonist, markedly reduced ΔpH in light with NO 3 − , NO 2 − , N 2 O, or O 2 as the terminal acceptor, indicating that photosynthetically generated electrons are used for denitrification in this bacterium.
    Type of Medium: Online Resource
    ISSN: 0829-8211 , 1208-6002
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1986
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Canadian Science Publishing ; 2016
    In:  Canadian Journal of Chemistry Vol. 94, No. 11 ( 2016-11), p. 936-939
    In: Canadian Journal of Chemistry, Canadian Science Publishing, Vol. 94, No. 11 ( 2016-11), p. 936-939
    Abstract: The family of galectin proteins involved in adhesion, growth regulation, immunity, and inflammatory events are important targets for development of small molecule antagonists. Here, N-sulfonyl amidine galactopyranoside derivatives obtained via a multicomponent reaction between galactose alkyne derivatives, sulfonyl azides, and amines were evaluated as antagonists of galectin-1, -2, -3, -4N (N-terminal domain), -4C (C-terminal domain), -8N, -9N, and -9C in a competitive fluorescence polarization assay. Highly selective compounds against galectin-9N with up to 30-fold improved affinity compared to the reference methyl β-d-galactopyranoside were identified. Molecular dynamics simulation suggested that the selectivity and affinity for galectin-9N originate from the N-sulfonyl amidine moieties forming tridentate hydrogen bonds to two asparagine side chains and one phenyl stacking edge-to-face to an arginine side chain. These selective galectin-9N antagonists are of significant value as chemical tools for studying galectin-9 biology and chemistry as well as possible starting structures for the discovery of galectin-9-targeting drugs influencing, e.g., immune regulation.
    Type of Medium: Online Resource
    ISSN: 0008-4042 , 1480-3291
    RVK:
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 2016
    detail.hit.zdb_id: 1482256-8
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  • 3
    Online Resource
    Online Resource
    Canadian Science Publishing ; 1986
    In:  Biochemistry and Cell Biology Vol. 64, No. 9 ( 1986-09-01), p. 946-952
    In: Biochemistry and Cell Biology, Canadian Science Publishing, Vol. 64, No. 9 ( 1986-09-01), p. 946-952
    Abstract: Washed cells of Rhodopseudomonas sphaeroides f.sp. denitrificans depleted of cellular K + by treatment with diethanolamine contained less than 5 mM K + . The K + -depleted cells accumulated 22 Na + only when there was no diethanolamine in the external buffer (50 mM Tris–HCl, pH 7.5). Studies with 22 Na + -loaded cells indicate that this photodenitrifier had antiporters for Na + –H + , K + –Na + , and K + –H + and lacked a respiration (denitrification) dependent Na + pump. The K + –Na + antiporter was electrogenic and required proton-motive force for its operation. Thus the addition of either NaCl or KCl to K + -depleted cells resulted in a depolarization of Δψ, both in light and in the dark, by 10–35 mV, which was partially compensated for by a concomitant increase (5–13 mV) in ΔpH.
    Type of Medium: Online Resource
    ISSN: 0829-8211 , 1208-6002
    Language: English
    Publisher: Canadian Science Publishing
    Publication Date: 1986
    SSG: 12
    Location Call Number Limitation Availability
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