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Mouse d-Amino-Acid Oxidase: Distribution and Physiological Substrates.

TLDR
The main physiological substrates of mouse DAO are d-alanine and d-serine, which are most abundant in the tissues and body fluids of mice.
Abstract
d-Amino-acid oxidase (DAO) catalyzes the oxidative deamination of d-amino acids. DAO is present in a wide variety of organisms and has important roles. Here, we review the distribution and physiological substrates of mouse DAO. Mouse DAO is present in the kidney, brain, and spinal cord, like DAOs in other mammals. However, in contrast to other animals, it is not present in the mouse liver. Recently, DAO has been detected in the neutrophils, retina, and small intestine in mice. To determine the physiological substrates of mouse DAO, mutant mice lacking DAO activity are helpful. As DAO has wide substrate specificity and degrades various d-amino acids, many d-amino acids accumulate in the tissues and body fluids of the mutant mice. These amino acids are d-methionine, d-alanine, d-serine, d-leucine, d-proline, d-phenylalanine, d-tyrosine, and d-citrulline. Even in wild-type mice, administration of DAO inhibitors elevates D-serine levels in the plasma and brain. Among the above d-amino acids, the main physiological substrates of mouse DAO are d-alanine and d-serine. These two d-amino acids are most abundant in the tissues and body fluids of mice. d-Alanine derives from bacteria and produces bactericidal reactive oxygen species by the action of DAO. d-Serine is synthesized by serine racemase and is present especially in the central nervous system, where it serves as a neuromodulator. DAO is responsible for the metabolism of d-serine. Since DAO has been implicated in the etiology of neuropsychiatric diseases, mouse DAO has been used as a representative model. Recent reports, however, suggest that mouse DAO is different from human DAO with respect to important properties.

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Chemogenetic generation of hydrogen peroxide in the heart induces severe cardiac dysfunction.

TL;DR: An in vivo chemogenetic approach is used to develop a heart failure model in which generation of hydrogen peroxide in the heart leads to systolic heart failure without fibrotic remodeling.
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Emerging Role of D-Amino Acid Metabolism in the Innate Defense.

TL;DR: Recent evidence is highlighted supporting the hypothesis that D-amino acids are utilized as inter-kingdom communication at host–microbe interface to modulate bacterial colonization and host defense.
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D-glutamate, D-serine, and D-alanine differ in their roles in cognitive decline in patients with Alzheimer's disease or mild cognitive impairment.

TL;DR: This is the first study suggesting that D-amino acids in blood may be correlated with ADAS-cog in different items and in the opposite direction, and lower D-glutamate and higher D-alanine levels may predict more behavioral symptoms.
References
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Journal ArticleDOI

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.

TL;DR: A map of 191 single-nucleotide polymorphism (SNPs) was built across a 5-Mb segment from chromosome 13q34 that has been genetically linked to schizophrenia, pointing to the involvement of this N-methyl-d-aspartate receptor regulation pathway in schizophrenia.
Journal ArticleDOI

Purification of serine racemase: Biosynthesis of the neuromodulator d-serine

TL;DR: Properties such as pH optimum, Km values, and the requirement for pyridoxal phosphate resemble those of bacterial racemases, suggesting that the biosynthetic pathway for D-amino acids is conserved from bacteria to mammalian brain.
Journal ArticleDOI

A novel pathway for the production of hydrogen sulfide from D-cysteine in mammalian cells

TL;DR: This study reveals that administration of D-cysteine protects primary cultures of cerebellar neurons from oxidative stress induced by hydrogen peroxide and attenuates ischaemia-reperfusion injury in the kidney more than L-Cysteine.
Journal ArticleDOI

Free D-aspartate and D-serine in the mammalian brain and periphery.

TL;DR: This review deals with the recent advances in the studies of presence of free D-aspartate and D-serine and their metabolic systems in mammals and shall discuss also the NMDA receptor and uptake system of D-amino acids.
Journal ArticleDOI

Physiological functions of D-amino acid oxidases: from yeast to humans

TL;DR: Current research is attempting to delineate the regulation of DAAO functions in the contest of complex biochemical and physiological networks.
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