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1 ased transcript levels, and the induction of alternative oxidase.
2 s a chloroplast homolog of the mitochondrial alternative oxidase.
3 dependent on both a cytochrome chain and an alternative oxidase.
4 nalling, as evidenced by the induction of an alternative oxidase.
6 -type RING finger) family protein and AOX1A (alternative oxidase 1a) protein groups, respectively.
7 otein with sequence motifs characteristic of alternative oxidase, a mitochondrial protein that functi
8 od1 plantlets is exclusively associated with alternative oxidase activity and that alternative NADH d
9 e c oxidase, and this uncoupling induces the alternative oxidase activity and the accumulation of rea
10 th the general relation between the apparent alternative oxidase activity and the climate of origin o
11 ook, adapted to the tropics, has very little alternative oxidase activity compared with wheat, adapte
12 levels of cyanide-insensitive mitochondrial alternative oxidase activity, (iii) cytochrome deficienc
14 ides a two-step catalytic precedent for the "alternative oxidase" activity recently proposed for a me
15 ntegrity was maintained, but accumulation of alternative oxidase and decreased abundance of lipoic ac
16 of alternative respiratory pathways, namely alternative oxidase and external NADH-dependent alternat
17 e only reliable method at present to measure alternative oxidase (AOX) activity is through measuremen
18 nase) bypassed complex I inhibition, whereas alternative oxidase (AOX) bypassed complex III or IV inh
21 We have examined the expression of three alternative oxidase (aox) genes in two types of maize mi
23 uncoupling mitochondria or by expressing the alternative oxidase (AOX) inhibits this inflammatory phe
29 eas the oxidation current increased when the alternative oxidase (AOX) pathway was blocked by salicyl
30 s1-1 allele causes the loss of mitochondrial alternative oxidase (AOX) protein that might be related
31 ri produces an NO-inducible and NO-resistant alternative oxidase (Aox) that allows respiration to con
32 ondrial electron transport chain includes an alternative oxidase (AOX) that is hypothesized to aid ph
33 tochondrial complex III/IV deficiencies with Alternative oxidase (AOX), however, fully restores ATP l
34 All higher plants and many fungi contain an alternative oxidase (AOX), which branches from the cytoc
40 tive oxygen species, and an induction of the alternative oxidase AOX1a and pathogenesis-related PR1 e
43 The expression and kinetic activity of the alternative oxidase are regulated by concentrations of k
45 terminal oxidases, cytochrome c oxidase and alternative oxidase, are present and constitutively acti
46 in A and cyanide excluded the presence of an alternative oxidase as described in other parasites.
47 lfide bond, because iodoacetate bound to the alternative oxidase at the activating site even when the
48 tate with sulfhydryls, the activation of the alternative oxidase by alpha-keto acids appears to invol
49 reduced ATP synthase amounts, and increased alternative oxidase capacity and led to specific long-te
50 3-1, not cbb3-2, inhibited expression of the alternative oxidase CioAB and thus influenced a signal t
51 ble holo-CI assembly/activity, showed higher alternative oxidase content/activity, and displayed a gr
52 of electron flow between Cyt oxidase and the alternative oxidase depends on the kinetic behavior of t
54 tants of aodA, dnmA, mnSOD and pimA encoding alternative oxidase, dynamin related protein, manganese
59 re up-regulated, and may coordinate with the alternative oxidases in the alternative respiratory path
60 reatment with complex III inhibitors and the alternative oxidase inhibitor, salicylhydroxamic acid (S
63 served effects of sulfhydryl reagents on the alternative oxidase of isolated soybean mitochondria wer
71 ntrol line, which suggests that changing the alternative oxidase protein level by genetic engineering
72 is role is supported by the observation that alternative oxidase protein levels often increase when p
73 g bean plants that up-regulated the level of alternative oxidase protein maintained a greater electro
74 to be more dependent on increased levels of alternative oxidase protein than changes in its oxidatio
75 her levels of Aox1 mRNA, increased levels of alternative oxidase protein(s), and an unusual higher mo
77 en was carried out to identify regulators of alternative oxidase (rao mutants), using AOX1a expressio
79 ein is only distantly related to these other alternative oxidases, suggesting that IM is a novel memb
83 olecular disulfide bond did not form and the alternative oxidase was present only as a noncovalently
84 e cDNAs as well as Aox1, a gene encoding the alternative oxidase, were found to also be strongly indu
85 ained a greater electron partitioning to the alternative oxidase when measured at temperatures below
86 egrees C was fully restored by expressing an alternative oxidase, which specifically bypasses the cyt
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