نتایج جستجو برای: coenzyme

تعداد نتایج: 18341  

Journal: :Andrologia 2014
R Festa E Giacchi S Raimondo L Tiano P Zuccarelli A Silvestrini E Meucci G P Littarru A Mancini

Many conditions associated with male infertility are inducers of oxidative stress, including varicocele. Antioxidants, such as coenzyme Q10, may be useful in this case. To evaluate the antioxidant capacity of seminal plasma of infertile men with varicocele before and after an oral supplementation with coenzyme Q10 , 38 patients were recruited from a pilot clinical trial. A standard semen analys...

Journal: :Organic & biomolecular chemistry 2015
Ke Xia Guang-Bin Shen Xiao-Qing Zhu

32 F420 coenzyme models with alkylation of the three different N atoms (N1, N3 and N10) in the core structure (XFH(-)) were designed and synthesized and the thermodynamic driving forces (defined in terms of the molar enthalpy changes or the standard redox potentials in this work) of the 32 XFH(-) releasing hydride ions, hydrogen atoms and electrons, the thermodynamic driving forces of the 32 XF...

Journal: :The Journal of biological chemistry 1948
D M HEGSTED F LIPMANN

Lipmann, Kaplan, Novelli, Tuttle, and Guirard (1) reported that, whereas concentrates of the coenzyme required for acetylation (coenzyme A) showed no pantothenic acid activity by the ordinary microbiological assay, considerable amounts of p-alanine were found after acid hydrolysis. From this early observation, it was suspected that the coenzyme might contain combined pantothenic acid which was ...

2015
Qiuhua Shen Janet D. Pierce

Type 2 diabetes mellitus (T2DM) is a major cause of morbidity and mortality with ever increasing prevalence in the United States and worldwide. There is growing body of evidence suggesting that mitochondrial dysfunction secondary to oxidative stress plays a critical role in the pathogenesis of T2DM. Coenzyme Q10 is an important micronutrient acting on the electron transport chain of the mitocho...

Journal: :Experimental gerontology 2004
José L Quiles Julio J Ochoa Jesús R Huertas José Mataix

This study investigates the usefulness of a long-term supplementation with coenzyme Q(10) in rats from the point of view of lifespan, DNA double-strand breaks and to assess whether this supplementation might attenuate oxidative alterations related to PUFA-rich diets, which would allow to preserve beneficial aspects of PUFA on health avoiding their deleterious aspects. Supplemented animals showe...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1983
D P Nagle R S Wolfe

Component A, the oxygen-sensitive protein fraction of the methyl coenzyme M methylreductase system of Methanobacterium thermoautotrophicum, has been stabilized and resolved into three protein fractions and one cofactor that are required to reconstitute component A activity. Component A1 is oxygen-stable and contains hydrogen-dependent deazaflavin (coenzyme F420)-reducing activity. Component A2 ...

Journal: :Science 2016
Kaiyuan Zheng Phong D Ngo Victoria L Owens Xue-Peng Yang Steven O Mansoorabadi

Methyl-coenzyme M reductase (MCR) is the key enzyme of methanogenesis and anaerobic methane oxidation. The activity of MCR is dependent on the unique nickel-containing tetrapyrrole known as coenzyme F430. We used comparative genomics to identify the coenzyme F430 biosynthesis (cfb) genes and characterized the encoded enzymes from Methanosarcina acetivorans C2A. The pathway involves nickelochela...

Journal: :The Journal of biological chemistry 1965
C F Howard J M Lowenstein

The synthesis de no2ro of fatty acids by particle-free cell extracts is inhibited by long chain fatty acyl coenzyme A derivatives such as palmityl coenzyme A (l-5). On the other hand, fatty acid synthesis is stimulated by the addition of microsomes (6-9). The enzymes that transfer long chain fatty acyl groups from coenzyme A to glycerol S-phosphate and its derivatives are also located in the mi...

Journal: :The Journal of biological chemistry 1968
K McCarthy W Lovenberg A Sjoerdsma

Thyroxine and related compounds have been found to be excellent inhibitors of horse liver alcohol dehydrogenase. The thyroid hormones appear to act by interfering with the normal coenzyme-binding mechanism. Triiodothyronine and thyroxine are uncompetitive inhibitors with regard to the coenzyme. In addition to inhibiting the enzyme activity, the thyroid hormone also quenches the enhanced fluores...

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