Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:1.10.3.3 (ascorbate oxidase)
 778 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The in vivo measurement of the rapid changes in the extracellular concentrations of L-glutamic acid in the mammalian brain during normal neuronal activity or following excessive release due to episodes of anoxia or ischemia has not been possible to this date. Current techniques for the measurement of the release of endogenous glutamate into the extracellular space of the central nervous system are relatively slow and do not measure the actual concentration of free glutamate in the extracellular space. An enzyme-based electrode with rapid response times (about 1 s) and high degree of sensitivity (less than 2 microM) and selectivity for L-glutamic acid is described in this paper. This electrode has both L-glutamate and ascorbate oxidase immobilized on its surface. The latter enzyme removes almost completely any interferences produced by the high levels of extracellular ascorbate present in brain tissue. The response of the electrode to glutamate and other potentially interfering substances was fully characterized in vitro and its selectivity, sensitivity and rapidity in responding to a rise in extracellular glutamate concentrations was also demonstrated in vivo. Placement of the electrode in the dentate gyrus of the hippocampus led to the detection of both KCl-induced release of L-glutamic acid and the release induced by stimulation of the axons in the perforant pathway. The development of this selective, sensitive and rapidly responding glutamate sensor should make it now possible to measure the dynamic events associated with glutamate neurotransmission in the central nervous system.
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PMID:Direct measurement of glutamate release in the brain using a dual enzyme-based electrochemical sensor. 782 Jun 52

Acetic acid and sodium acetate are generally supplied to wastewater treatment plants (WWTPs) in China to improve total nitrogen (TN) and total phosphorus (TP) removal, and the addition of carbon source also facilitates to increase sludge growth rate and further provides material basis for the extraction of proteins and amino acids from activated sludge. To recycle ammonia nitrogen resources, a system that combined adsorption and anaerobic-anoxic-oxic (A/AAO) process for treating low strength wastewater was established. Experimental results showed that by the addition of carbon substrate from a mixture of anaerobically fermented adsorption sludge, the average removal efficiency of chemical oxygen demand (COD), ammonia nitrogen, TN, and TP were 88%, 96.9%, 93.9%, and 92.1%, respectively, and the ratio of nitrogen assimilation to nitrogen dissimilation significantly increased by a factor of 2.5. Through energy analysis (based on adenosine triphosphate, ATP), sludge flocculation capacity and settling property, it was found that the AAO process sludge presented the logarithmic growth characteristics. The respective sludge protein and amino acids contents increased by over 11.4% and 40.3%, and the synthetic products of glutamic acid, alanine and aspartate increased through the assimilation of ammonia nitrogen, thereby indicating that replenishing the carbon substrate could markedly enhance protein and amino acids contents in AAO process sludge. Moreover, the diversity of the microbial community in adsorption process was relatively rich, the diversity in the adsorption process sludge was the highest, while the diversity of the AAO process sludge evidently decreased. The microbial community in each process was similarly based on 16S rDNA gene sequence analysis, microflora was prominent in the AAO process, with Dechloromonas, Flavobacterium, Zoogloea, Unclassified_Rhodocyclaceae and Thauera as the dominant species. Promising carbon utilization facilitates contaminants removal in low strength wastewater treatment and is conducive to protein production through ammonia nitrogen assimilation.
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PMID:Promising carbon utilization for nitrogen recovery in low strength wastewater treatment: Ammonia nitrogen assimilation, protein production and microbial community structure. 3205 Mar 65