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1 he efflux systems are ATPases and others are chemiosmotic cation/proton antiporters.
2 opose that periplasmic P(i) anions pair with chemiosmotic cations of the PMF and millions of accumula
3     The coexistence of Na(+) and H(+)-driven chemiosmotic circuits has implications for salt and pH r
4 copic method to investigate the mechanism of chemiosmotic coupling in secondary active transporters.
5                                              Chemiosmotic coupling is universal: practically all cell
6 osed function of Ech as an ion-translocating chemiosmotic coupling site has neither been demonstrated
7                          The universality of chemiosmotic coupling suggests that it arose very early
8                                           In chemiosmotic coupling, a transmembrane ion gradient is u
9 cal origins that account for the ubiquity of chemiosmotic coupling, and Na(+)/H(+) transporters in pa
10 mes, suggesting a possible abiotic origin of chemiosmotic coupling.
11 triple-polypeptide Czc (Cd2+, Zn2+ and Co2+) chemiosmotic efflux pump consists of inner membrane (Czc
12 e three-component Czc (Cd2+, Zn2+, and CO2+) chemiosmotic efflux pump of soil microbes consists of in
13 ely linked to genes encoding three-component chemiosmotic efflux pumps that export heavy metals or to
14 uss the diversity of ETCs and other forms of chemiosmotic energy conservation, describe current work
15 the membranes, thereby providing a source of chemiosmotic energy for primitive metabolic reactions.
16 electron transport are ubiquitous sources of chemiosmotic energy in all life today, but how this syst
17 ylhydrazone, suggesting the involvement of a chemiosmotic gradient.
18     These findings are inconsistent with the chemiosmotic hypothesis for auxin transport.
19 idification of cell wall compartments to the chemiosmotic hypothesis of auxin transport.
20 ing sites in microorganisms that depend on a chemiosmotic mechanism for energy conservation.
21 ies on the additional formation of ATP via a chemiosmotic mechanism.
22 ide fixation with the synthesis of ATP via a chemiosmotic mechanism.
23 , bacteriorhodopsins capable of generating a chemiosmotic membrane potential in response to light hav
24                                   Mitchell's chemiosmotic model of energy coupling posits a bulk elec
25 librium thermodynamics in the context of the chemiosmotic model of proton translocation and energy co
26      Mitochondrial ATP synthase is driven by chemiosmotic oxidation of pyruvate derived from glycolys
27                             According to the chemiosmotic polar diffusion hypothesis, auxin pulse vel
28 ly), hydrogen use to drive acetogenesis, and chemiosmotic potential generation via respiratory (type
29                             The basis of the chemiosmotic theory is that energy from light or respira
30                  This article integrates the chemiosmotic theory of energy transduction with the meth
31 ectrochemical gradient, as postulated by the chemiosmotic theory of Peter Mitchell.
32 esults are discussed in a general context of chemiosmotic theory.
33 a single polypeptide (ArsB) functioning as a chemiosmotic transporter.
34 a single-polypeptide (ArsB) functioning as a chemiosmotic transporter.