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»).»
This toxin stops the cell respiration as a non-competitive inhibitor for an enzyme in the mitochondria that is referred to as
cytochrome c oxidase, causing asphyxiation in the cells.
In your mitochondria, there's also a specific molecule called
cytochrome c oxidase, which is involved in the energy production within the mitochondria.
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.
The important thing to understand is that LLLT works by activating a very important enzyme known as «
cytochrome c oxidase»... which plays a crucial role in healthy metabolism and energy production.
Light therapy (how we use it) helps activate an important metabolic enzyme called
cytochrome c oxidase, which is essential for healthy cellular energy production, and relaxation.
Red to infra - red light has been shown to effectively activate an important metabolic enzyme known as
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.
And
Cytochrome C Oxidase is a heme protein just like hemoglobin in our skin.
Hybrid broadband NIRS / Diffuse correlation spectroscopy system for simultaneous monitoring of cerebral perfusion and
cytochrome c oxidase
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.
Molecular evolution of
the cytochrome c oxidase subunit 5A gene in primates.
This protein is one of the nuclear - coded polypeptide chains of
cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
Cytochrome c oxidase is part of Complex IV.
A famous example from the superfamily is
cytochrome c oxidase, the last enzyme in the respiratory electron transport chain located in the mitochondrial membrane (see graph).
Knockdown of human COX17 affects assembly and supramolecular organization of
cytochrome c oxidase.
Chronic treatment with azide in situ leads to an irreversible loss of
cytochrome c oxidase activity via holoenzyme dissociation.
They can not replace damaged mitochoondrial proteins, but for the most part, they are pretty resistant to oxidative damage (particularly
cytochrome c oxidase which is very oxidative damage resistant, much more so than is DNA).
Adaptive evolution of
cytochrome c oxidase: infrastructure for a carnivorous plant radiation Jobson, R. W., R. Nielsen, L. Laakkonen, M. Wikström et al. 2004.
Adaptive evolution of
cytochrome c oxidase: infrastructure for a carnivorous plant radiation.
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.
Not exact matches
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.
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).
When
cytochrome c -
oxidase and NADH are activated by laser light they increase the synthesis of ATP, accelerating cellular function.