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1 ratio and reduced oxygen consumption via the alternative oxidase.
2 atus and increased electron transfer through alternative oxidase.
3 nalling, as evidenced by the induction of an alternative oxidase.
4 ased transcript levels, and the induction of alternative oxidase.
5 s a chloroplast homolog of the mitochondrial alternative oxidase.
6 dependent on both a cytochrome chain and an alternative oxidase.
7 rabidopsis thaliana mutants of mitochondrial alternative oxidase 1a (aox1a) in response to the model
9 -type RING finger) family protein and AOX1A (alternative oxidase 1a) protein groups, respectively.
10 otein with sequence motifs characteristic of alternative oxidase, a mitochondrial protein that functi
11 od1 plantlets is exclusively associated with alternative oxidase activity and that alternative NADH d
12 e c oxidase, and this uncoupling induces the alternative oxidase activity and the accumulation of rea
13 th the general relation between the apparent alternative oxidase activity and the climate of origin o
14 ook, adapted to the tropics, has very little alternative oxidase activity compared with wheat, adapte
15 levels of cyanide-insensitive mitochondrial alternative oxidase activity, (iii) cytochrome deficienc
17 ides a two-step catalytic precedent for the "alternative oxidase" activity recently proposed for a me
18 ed activity against T. brucei overexpressing alternative oxidase and against Trypanosoma congolense s
20 ntegrity was maintained, but accumulation of alternative oxidase and decreased abundance of lipoic ac
21 of alternative respiratory pathways, namely alternative oxidase and external NADH-dependent alternat
22 ia targeted changes to the expression of the alternative oxidase and mitochondrial uncoupling pathway
23 e only reliable method at present to measure alternative oxidase (AOX) activity is through measuremen
25 nase) bypassed complex I inhibition, whereas alternative oxidase (AOX) bypassed complex III or IV inh
28 We have examined the expression of three alternative oxidase (aox) genes in two types of maize mi
29 e (COX), we expressed the non-proton-pumping alternative oxidase (AOX) in activated COX-deficient T c
32 uncoupling mitochondria or by expressing the alternative oxidase (AOX) inhibits this inflammatory phe
37 that during cold conditioning, activation of alternative oxidase (AOX) occurs pre-climacterically.
40 eas the oxidation current increased when the alternative oxidase (AOX) pathway was blocked by salicyl
42 s1-1 allele causes the loss of mitochondrial alternative oxidase (AOX) protein that might be related
43 ri produces an NO-inducible and NO-resistant alternative oxidase (Aox) that allows respiration to con
44 ondrial electron transport chain includes an alternative oxidase (AOX) that is hypothesized to aid ph
45 piration without generating superoxide using alternative oxidase (AOX) was not sufficient to reverse
46 by ectopic expression of Ciona intestinalis alternative oxidase (AOX)(12), which also oxidizes ubiqu
47 w from the cytochrome-mediated pathway to an alternative oxidase (AOX), an increase in proline consum
48 tochondrial complex III/IV deficiencies with Alternative oxidase (AOX), however, fully restores ATP l
50 All higher plants and many fungi contain an alternative oxidase (AOX), which branches from the cytoc
51 rocess was delayed in cells transfected with alternative oxidase (AOX), which combines the functions
52 Mcp1 model with xenotopic expression of the alternative oxidase (AOX), which provides a sink for ele
59 tive oxygen species, and an induction of the alternative oxidase AOX1a and pathogenesis-related PR1 e
60 ombined stress, where tapped key genes (e.g. alternative oxidase, Aox1a) need further functional anal
63 Accumulating MDS gene products, including alternative oxidases (AOXs), affect redox status of the
64 The expression and kinetic activity of the alternative oxidase are regulated by concentrations of k
66 terminal oxidases, cytochrome c oxidase and alternative oxidase, are present and constitutively acti
67 in A and cyanide excluded the presence of an alternative oxidase as described in other parasites.
68 lfide bond, because iodoacetate bound to the alternative oxidase at the activating site even when the
69 tate with sulfhydryls, the activation of the alternative oxidase by alpha-keto acids appears to invol
70 reduced ATP synthase amounts, and increased alternative oxidase capacity and led to specific long-te
71 3-1, not cbb3-2, inhibited expression of the alternative oxidase CioAB and thus influenced a signal t
72 ble holo-CI assembly/activity, showed higher alternative oxidase content/activity, and displayed a gr
73 of electron flow between Cyt oxidase and the alternative oxidase depends on the kinetic behavior of t
75 tants of aodA, dnmA, mnSOD and pimA encoding alternative oxidase, dynamin related protein, manganese
82 re up-regulated, and may coordinate with the alternative oxidases in the alternative respiratory path
83 reatment with complex III inhibitors and the alternative oxidase inhibitor, salicylhydroxamic acid (S
87 served effects of sulfhydryl reagents on the alternative oxidase of isolated soybean mitochondria wer
96 ntrol line, which suggests that changing the alternative oxidase protein level by genetic engineering
97 is role is supported by the observation that alternative oxidase protein levels often increase when p
98 g bean plants that up-regulated the level of alternative oxidase protein maintained a greater electro
99 to be more dependent on increased levels of alternative oxidase protein than changes in its oxidatio
100 her levels of Aox1 mRNA, increased levels of alternative oxidase protein(s), and an unusual higher mo
102 en was carried out to identify regulators of alternative oxidase (rao mutants), using AOX1a expressio
103 ng of mitochondrial electron transfer to the alternative oxidase, reduced growth rate and cellular AT
105 ein is only distantly related to these other alternative oxidases, suggesting that IM is a novel memb
107 somal glycerol kinase (TGK) and trypanosomal alternative oxidase (TAO) is considered a validated stra
110 olecular disulfide bond did not form and the alternative oxidase was present only as a noncovalently
111 e cDNAs as well as Aox1, a gene encoding the alternative oxidase, were found to also be strongly indu
112 ained a greater electron partitioning to the alternative oxidase when measured at temperatures below
113 H dehydrogenase (NDI1) or Ciona intestinalis alternative oxidase, which can complement the functional
114 egrees C was fully restored by expressing an alternative oxidase, which specifically bypasses the cyt