160 resultados para Coenzime Q10


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辅酶Q10存在于生物体呼吸链中,化学名称为2,3-二甲氧基-5-甲基-6-癸异戊烯基苯醌,是人体内存在的唯一泛酮类化合物,具有广泛的临床应用。本论文即应用微生物发酵法提取辅酶Q10以期为进一步扩大辅酶Q10生产规模提供基础理论和实验指导。本研究选择皂化抽提辅酶Q10结合高效液相色谱定量分析方法对文献报道的辅酶Q10产生菌进行筛选比较,最终选择根癌土壤杆菌AGR1.1416为出发菌株,对其进行诱变处理,筛选到酪氨酸、色氨酸双重营养缺陷的抗乙硫氨酸突变株AGR0610,产量达到31.42mg/L,比原始菌株提高了156.07%。通过单因素实验考察了碳源、氮源、初始pH值、接种量、装液量、温度和培养时间等发酵条件对一辅酶Q10产量的影响,结果表明,以葡萄糖和糖蜜为复合碳源,酵母膏和大豆蛋白陈为复合氮源,在30℃下,初始pH为7.0时,以7%的接种量接入到装有20OmL培养基的50OmL三角瓶中,培养72h,菌体生长良好,辅酶Q10产量可达到最大值。应用Placket-burman法对影响突变株AGR0610发酵产辅酶Q10的碳源、氮源和添加物等因素进行考察,表明糖蜜、大豆蛋白陈、蛋氨酸和玉米浆对辅酶Q10发酵有显著影响。应用响应曲面法对这四种因素的最佳取值水平范围和交互影响作用进行分析,结果表明,玉米浆与糖蜜、大豆蛋白陈之间的交互作用有显著影响,当糖蜜为1.02%,大豆蛋白陈为0.49%,蛋氨酸为0.34%,玉米浆为0.29%时,辅酶Q10有最大产量38.42mg/L。优化后的辅酶Q10产量比优化前提高了23.86%,达到国内先进水平。原始菌株经诱变,发酵条件优化使产量提高了215.69%。辅酶Q10粗提品经制备薄层层析分离纯化,结晶,得到辅酶Q10纯品,回收率达到90%以上。

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本文根据我们实验室建立的发酵产物中辅酶Q10定性定量检测方法,筛选得到一株可以代谢产生较多辅酶Q10的野生菌株放射形土壤杆菌(Agrobacterium radiobacter No.50)。 为了提高放射形土壤杆菌的辅酶Q10的产量,本实验利用液体培养研究了单因素对菌株辅酶Q10产量的影响,并用正交法确定了最佳液态发酵条件。最佳发酵培养基是:葡萄糖20g,蔗糖40g, 硫酸铵10g,玉米浆30g, 酵母膏3g,K2HPO4 3g,MgSO4.7H2O 1g,蒸馏水1000mL,pH 7.0-7.2。最佳发酵条件是:转接斜面菌种到种子培养基, 转速220r/min、温度28。C培养24h后,转入发酵培养基(250mL三角拼装液量为50mL,pH 7.0), 接种量为10%,转速220r/min、温度28。C,培养120h。在此条件下,菌体湿重约为50g/L,辅酶Q10含量约为20mg/L。 本文以放射形土壤杆菌为出发菌株进行诱变育种,以期获得辅酶Q10高产菌。根据微生物育种原理、参照辅酶Q10的代谢调控机制,以野生型放射形土壤杆菌(Agrobacterium radiobacter No.50)为出发菌株,采用紫外线和亚硝基胍复合诱变技术,依次筛选得到菌体提取物M抗性菌ARM-7、烟草提取物T抗性菌株ARMT-26、Vk3抗性菌株ARMTV-25、链霉素抗性菌株ARMTVS-32,菌株ARMTVS-32产量达到了36.8mg/L,与原始出发菌株相比,产量提高了77%。 研究了茄尼醇、对羟基苯甲酸、橘子皮提取物D、胡萝卜提取物E、烟草提取物对ARMTVS-32合成辅酶Q10的影响,结果表明这些物质对菌体合成辅酶Q10有一定促进作用,添加0.2g/L茄尼醇时,辅酶Q10含量提高了17%,达到了40.7mg/L;添加1.2g/L橘子皮提取物D时,辅酶Q10含量提高了13.8%,达到了39.6mg/L;添加0.5g/L胡萝卜提取物E时,辅酶Q10含量提高了25.3% ,达到了43.6mg/L;添加8g/L烟草提取物时,辅酶Q10含量提高了12.6%,达到了39.2mg/L。 Production of Coenzyme- Q10 (CoQ10) by fermentation is considered as a process with broad prospects.Quantitative Analysis of CoQ10 in the culture of microbe by TLC—UV spectrophotometry was developed, by using this method we got the strain Agrobacterium radiobacter,which was isolated from forest soil of southwest of China. The effect of the single factor on CoQ10-production ability of the strain was examined by liquid cultured, and its best optimum cultivation conditions were established by orthogonal method. The results showed that the optimum fermentation conditions were as following: carbon sources glucose 20g/L,sucrose 40g/L; nitrongen sources (NH4)2SO4 10g/L,maize liquid 30g/L;yeast extract 3g; K2HPO4 3g/L,MgSO4.7H2O 1g/L; initial pH was 7 and volume of medium(medium volume vs flask volume) was 50mL/500mL, incubating for 120h on a rotary shaker at 220 rpm and 28℃.Under these conditions, the biomass and CoQ10 concentration reached 50g/L and 20mg/L respectively. According to the biosynthesis mechanism of CoQ10 and breeding theory, CoQ10 over-production strains were screened by UV--NTG. mutation using Agrobacterium radiobacter No.50 as parent strain. A microbe-juice resistant mutant ARMTVS-32, which also could resist tobacco-juice, VK3 and streptomycin, was screened out from an agar plate. The CoQ10 content of ARMTVS-32 reached 36.8mg/L, which was 77% higher than the initial strain. In addition, We discussed the effects of some organic substrates on the synthesis of CoQ10 in ARMTVS-32. The results showed that solanesol, orange juice D, carrot juice E and tobacco juice could promote the CoQ10 accumulation in the cells. The CoQ10 content of ARMTVS-32 reached 40.7mg/L when added 0.2g/L solanesol,it reached 39.6mg/L when added 1.2g/L orange juice D,it reached 43.6mg/L when added 0.5g/L carrot juice E. it reached 39.2mg/L when added 8g/L tobacco juice.

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Introduction: skeletal muscles are dynamic tissue that can change their phenotypic characteristics providing a better functional adaptation to different stimuli. L-thyroxine is a hormone produced by the thyroid gland and has been used as an experimental model for stimulation of oxidative stress in skeletal muscle. Coenzyme Q10 (CoQ10) is a fat-soluble provitamin endogenously synthesized and found naturally in foods such red meat, fish, cereals, broccoli and spinach. It has antioxidant properties and potential in the treatment of degenerative and neuromuscular diseases. Objective: to evaluate the protective effect of CoQ10 in the soleus muscle of rats against the oxidative damage caused by L-thyroxine. Methods: the rats were divided in four groups of six animals each: Group 1 (control); Group 2 (coenzyme Q10); Group 3 (L-thyroxine), and Group 4 coenzyme Q10 and L-thyroxine). After euthanasia, blood was collected and serum activity of the enzymes creatine kinase (CK) and aspartate aminotransferase (AST) was analyzed. In the soleus muscle homogenates the factors related to oxidative stress were assessed. Results: CoQ10 protected the soleus muscle against the damage caused by L-thyroxine and favored the maintenance of the antioxidant enzymes glutathione reductase and glutathione peroxidase, the concentration of decreased and oxidized glutathione, and prevented lipid peroxidation. Conclusion: the results indicate that CoQ10 protects rat soleus muscle from oxidative damage caused by L-thyroxine.

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Chronic myelogenous leukemia (CML) is a common myeloproliferative disease that is characterized by the clonal expansion of marrow stem cells, and is associated with the Philadelphia chromosome. As the disease progresses, additional chromosome abnormalities may arise. The prognostic impact of secondary chromosomal abnormalities in CML is complex, heterogeneous, and sometimes related to previous treatment. Here, we describe a CML patient in lymphoid blast crisis associated with a new chromosomal abnormality identified, dic(7;12)(p12.21;p12.2) and i(12)(q10) using classical cytogenetics and spectral karyotype analysis. To the best of our knowledge, this is the first report of t(7;12)(p11.1;q11.1) and i(12)(q10) in a CML patient with lymphoid evolution.

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The aim of our study was to investigate the relationships between the levels of coenzyme Q10 (CoQ10) and vitamin E and the levels of hydroperoxide in three subfractions of low density lipoproteins (LDL) that were isolated from healthy donors. LDL3, the densest of the three subfractions, has shown statistically significant lower levels of CoQ10 and vitamin E, which were associated with higher hydroperoxide levels when compared with the lighter counterparts. After CoQ10 supplementation, all three LDL subfractions had significantly increased CoQ10 levels. In particular, LDL3 showed the highest CoQ10 increase when compared with LDL1 and LDL2 and was associated with a significant decrease in hydroperoxide level. These results support the hypothesis that the CoQ10 endowment in subfractions of LDL affects their oxidizability, and they have important implications for the treatment of disease.