(1988) containing the papers presented at a meeting organized by the two of us and held in Rome and in the Convent of Santa Teresa (Caprarola) where the structure - function relationships and the physiopathology
of cytochrome oxidase were discussed in depth.
Two haplotypes (genetic variants)
of the Cytochrome Oxidase Type I sequence were detected: the «World haplotype» found in France, New Caledonia, French Polynesia, Singapore, Puerto Rico and Florida; and the «Australian haplotype» found in Australia.
Not exact matches
The terminal
cytochrome oxidase is the main membrane enzyme responsible for the human mitochondrial respiration and was thought to be used for the breath
of E. coli as well.
Each cell in our body «breathes» due to the work
of only the
cytochrome - c
oxidase, others we have not.
However, the E. coli bacteria has two types
of oxidase: bo - type
cytochrome oxidase (analogue
of «human»
cytochrome - c
oxidase) and completely different bd - type
cytochromes.
Among the other genes she says play a role in thoroughbred performance are peroxisome proliferator - activated receptor - γ coactivator - 1 alpha (PGC - 1α), which is involved in skeletal muscle adaptation to exercise; pyruvate dehydrogenase kinase, isozyme 4 (PDK4), involved in glucose regulation, expression
of which increased almost fourfold after sprints; and
cytochrome c
oxidase subunit 4 isoform 2 (COX 4I2), involved in respiration.
Adaptive evolution
of cytochrome c
oxidase: infrastructure for a carnivorous plant radiation.
Adaptive evolution
of cytochrome c
oxidase: infrastructure for a carnivorous plant radiation Jobson, R. W., R. Nielsen, L. Laakkonen, M. Wikström et al. 2004.
Chronic treatment with azide in situ leads to an irreversible loss
of cytochrome c
oxidase activity via holoenzyme dissociation.
Knockdown
of human COX17 affects assembly and supramolecular organization
of cytochrome c
oxidase.
In recent years, Michel and his research group mainly studied two types
of oxygen reductases: the so - called superfamily
of «heme - copper
oxidases», and the «
cytochrome bd
oxidase».
Cytochrome c
oxidase is part
of Complex IV.
This protein is one
of the nuclear - coded polypeptide chains
of cytochrome c
oxidase, the terminal
oxidase in mitochondrial electron transport.
Molecular evolution
of the
cytochrome c
oxidase subunit 5A gene in primates.
DNA barcoding aims to provide an efficient method for species - level identifications using an array
of species specific molecular tags derived from the 5 ′ region
of the mitochondrial
cytochrome c
oxidase I (COI) gene.
Certain particle compounds may directly generate ROS in vivo because
of their surface chemistry (eg, metals, organic compounds, and semiquinones) or after bioactivation by
cytochrome P450 systems (eg, polycyclic aromatic hydrocarbon conversion to quinones).6, 290 a, 290 b A particle surface or anions present on otherwise more inert particles may disrupt iron homeostasis in the lung and thereby also generate ROS via Fenton reactions.291 Other PM constituents may do so indirectly by the upregulation
of endogenous cellular sources (eg, nicotinamide adenine dinucleotide phosphate [NADPH]-RRB-
oxidase) 292,293 or by perturbing organelle function (eg, mitochondria) by taken - up PM components.261 Particle stimulation
of irritant and afferent ANS fibers may also play a role in local and systemic oxidative stress formation.294 Given the rich antioxidant defenses in the lung fluid, secondarily generated oxidization products
of endogenous molecules (eg, oxidized phospholipids, proteins) or a reduction in endogenous antioxidants per se may be responsible at least in part for the state
of oxidative stress in the lungs (along with instigating the subsequent cellular responses) rather than ROS derived directly from PM and its constituents.
Hybrid broadband NIRS / Diffuse correlation spectroscopy system for simultaneous monitoring
of cerebral perfusion and
cytochrome c
oxidase
It's a function
of the protein in the intermitochondrial membrane called uh —
Cytochrome C
Oxidase which I think most people know.
It is a cofactor in several oxidative enzymes vital to the function
of hematopoietic, vascular and skeletal tissues, as well as the structure and function
of the nervous system, including superoxide dismutase (oxygen radical scavenger),
cytochrome - c
oxidase (mitochondrial respiration), lysyl
oxidase (collagen and elastin synthesis) and ceruloplasmin ferroxidase / haephestin (iron metabolism).
It helps to stimulate
cytochrome c
oxidase enzyme and increase ATP (adenosine triphosphate) in your tissue, which is your primary source
of high energy production.
«By stimulating the
cytochrome oxidase enzyme, we are utilizing that oxygen in the respiratory chain inside
of the mitochondria, producing more ATP for that cell.
The copper - dependent enzyme
cytochrome oxidase, when low in the brains
of animal models, is the suspected cause
of suppressed myelin formation.
Fatty Acid
Oxidase, cytochrome oxidase, peroxidase, Catalase and Transhydrogenase are enzymes found in barley grass juice that help the decomposition of fats in the body proceed smoothly which also helps to promote correct body weight; without these enzymes, weight gain r
Oxidase,
cytochrome oxidase, peroxidase, Catalase and Transhydrogenase are enzymes found in barley grass juice that help the decomposition of fats in the body proceed smoothly which also helps to promote correct body weight; without these enzymes, weight gain r
oxidase, peroxidase, Catalase and Transhydrogenase are enzymes found in barley grass juice that help the decomposition
of fats in the body proceed smoothly which also helps to promote correct body weight; without these enzymes, weight gain results.
When
cytochrome c -
oxidase and NADH are activated by laser light they increase the synthesis
of ATP, accelerating cellular function.
Below is a sequence
of the barcode region
Cytochrome oxidase subunit 1 (COI or COX1) from a member
of the species.
Below is the sequence
of the barcode region
Cytochrome oxidase subunit 1 (COI or COX1) from a member
of the species.
The heart
of the innovation, as I understand it, lies in the choice
of a particular and small region
of DNA shared by many animals; to say it in technical terms: it's «a 648 base - pair region in the mitochondrial
cytochrome c
oxidase 1 gene («CO1»).»