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amino acid相关的网络例句

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与 amino acid 相关的网络例句 [注:此内容来源于网络,仅供参考]

Using the earthworm processed bean cake, many kinds of amino acid contents had the varying degree to increase in the reactant, the amino acid total quantity rosed 27.83% and each kind of essential amino acids' proportion also hastened reasonably.

利用蚯蚓处理豆粕,反应物中多种氨基酸含量均有不同程度增加,氨基酸总量与豆粕相比上升了27.83%,而且各种必需氨基酸的比例也更趋合理。

At first,the amino group of amino acid esters interacts with the carboxyl group of the amino acid residue of this porphyrinatozinc to form 1:1 adducts.

氨基酸酯的氨基首先与氨基酸残基的羧基作用形成1:1的加合物,然后与锌卟啉的中央锌原子配位形成1:2的加合物,客体分子与主体分子上的氨基酸残基之间的排斥作用以及主客体之间的色散力作用是主体分子能识别客体分子的另外两种作用。

According to nutritional evaluation in amino score and chemical score, the first limited amino acids were, the essential amino acid index was 69.02. The content of poyunsaturated fatty acid in fatty acids was 23.6%, which was higher than that in other economic fishes. It was indicated that Hemibarbus maculates Bleeker is one of freshwater fishes with better nutritive value.

氨基酸评分和化学评分均显示,花蟹蛋白质的第一限制性氨基酸为,必需氨基酸指数为69.02,脂肪酸中含有高比例(23.6%)的多不饱和脂肪酸,高于鲤科其它名优养殖鱼类。

Compared with the GPAT amino acid among squash, figleaf gourd, Arabidopsis thaliana, spinach, pea, redflow, etc., some sites of amino acid are the same in chill-resistant plants but different from squash, figleaf gourd and cucumber. These amino acids may also related to the selectivity of GPAT to different fatty acids in different plants.

比较南瓜、黑子南瓜、豌豆、红花、拟南芥菜和菠菜等植物中GPAT基因推导的氨基酸序列发现,在比较抗冷的拟南芥菜、红花、豌豆和菠菜等植物中,虽然它们之间的亲缘关系都比较远,但某些位点上的氨基酸残基却完全相同,而与南瓜等抗冷性较差的植物不同,这些位点的氨基酸残基可能也与GPAT对底物酰基的选择性有关。

Therelationship of the amount of catalyst and the ee% of product was seen to be negative nonlin-ear. Catalyst 3 was used in the enantioselective addition of diethylzinc to aromatic aldehydesand gave good results. The configuration of products was determined by the configuration ofthe catalysts' chiral carbon linked with hydroxy group. Using β- amino alcohols bearing only one chiral center as catalysts for the enantiose-lective addition were studied. D-N, N-dialkyl-2-amino butanol gave poor catalytic effect be-cause of their structure. The configuration of the product is the same as the catalyst. Anotherkind of β- amino alcohols - phenylglycine derivatives and valine derivatives have chiralcenter on the carbon linked with amino group. Catalyzed by-phenylglycine derivatives 6,7, 9, 10, the reactions gave satisfied results. The optical yields exceeded 80%.

在探讨了含有两个手性中心的β-氨基醇之后,选择了只有一个手性中心的β-氨基醇,一是手性中心为连羟基的手性碳原子:D-N,N-二烷基-2-氨基丁醇;二是手性中心为连氨基的手性碳原子:D-苯基甘氨酸衍生物和L-缬氨酸衍生物。D-2-氨基丁醇的催化效果不太好,这与其结构的空间位阻较小有关系,反应产物与连羟基手性碳构型一致;由苯基甘氨酸和缬氨酸出发合成五种β-氨基醇6-10,研究了不同ee%的-6作用下的二乙基锌-苯甲醛加成反应,发现该催化剂具有不对称放大效应;-7,9,lO的催化效果也比较令人满意,光学产率80%以上,所得产物构型与催化剂构型一致。

The determination of amino acids in blood clam antianaemia oral liquid using HPLC-AccQ-Tag method is reported. The oral liquid reacted with 6-aminoquinolyl-N-hydroxysuccini-mdyl carbamate. Then, the corresponding derivatives were analyzed with an HPLC. The chromatographic conditions were AccQ-TagTM C18 column for amino acids analysis (3.9mm×15cm); mobile phase of program elution sodium acetate solution(pH5.02), acetonitrile, Milli-Q water. The amino acids'AQC deriatives were detected at 248nm with a UV-detector. Eighteen kinds of amino acids were completely determined in 35 minutes.

以6-氨基喹啉-N-羟基琥珀酰亚胺基氨基甲酸酯为衍生剂,与毛蚶抗贫血口服液中的氨基酸柱前定量衍生,用WatersHPLC仪,AccQ-TagTM专用C18柱(3.9mm×15cm),以140mmol·L-1的醋酸钠溶液(pH5.02)为溶剂A,乙腈为溶剂B,超纯水为溶剂C,进行梯度洗脱,检测波长为248nm,35min测试完毕。

In order to research the relations of carbon sources to structure of PHAs, six kinds of PHAs sample were synthesized by activated sludge with six different carbon sources respectively in the aerobic-anaerobic-anoxic process. Their structures were determined by 〓HNMR、〓CNMR and GC-MS. When the carbon source was acetate, the unit composition of PHAs was 93. 91mol% 3-hydroxybutanoic acid and 6. 09mol% 3-hydroxypentanoic acid ; When the carbon source was propionate, the unit composition of PHAs was 28. 66mol% HB, 63. 13mol%HV, 2. 55mol% 2-methy-3-hydroxy-butanoic acid (2MHB) and 5. 66mol% 2-methyl-3-hydroxypentanoic acid (2MHV); When the carbon source was 80% butyrate and 20% 1, 4-butanediol, the unit composition of PHAs was 65. 03mol% HB, 28. 06mol%HV, 1. 91mol%2MHB, 2. 69mol% 2MHV, 0.73mol% 4-hydroxy butanoic acid (4HB), 0.78mol% 4-methyl-3-hydroxy-pentanoic acid (4MHV), 0.80mol% 3-hydroxyhexanoic acid ; When the carbon source was 20% butyrate and 80% 1, 4-butanediol, the unit composition of PHAs was 61. 39mol% HB, 23. 01mol%HV, 4. 58mol%2MHB, 5. 97mol% 2MHV, 0.91mol% 4HB, 2. 37mol% 4MHV, 1. 77mol% HHx; When the carbon source was 60% pentanoate and 40%glucose, the unit composition of PHAs was 41. 24mol% HB, 58. 76mol%HV; When the carbon source was 60% benzoate and 40% glucose, the unit composition of PHAs was 65. 48mol% HB and 34. 52mol% HV.

为了研究不同碳源与产物PHAs结构的关系,采用好氧-厌氧-缺氧模式利用6种不同碳源培养活性污泥得到6种不同的PHAs样品,通过〓HNMR、〓CNMR和GC-MS谱图确定了这6种PHAs的单体成分和比例:以乙酸钠培养活性污泥得到的PHAs的单体组成是93.91mol%3-羟基丁酸和6.09mol%3-羟基戊酸;以丙酸钠培养活性污泥得到的PHAs的单体组成除28.66mol%HB、63.13mol%HV外,另外还有2.55mol%3-羟基2-甲基丁酸(2MHB)和5.66mol%3-羟基2-甲基戊酸(2MHV);以80%丁酸钠和20%1,4-丁二醇混合溶液培养活性污泥得到的PHAs含有七种单体组成:65.03mol%HB,28.06mol%HV,1.91mol%2MHB,2.69mol%2MHV,0.73mol%4-HB(4-羟基丁酸),0.78mol%4MHV(3-羟基-4-甲基戊酸),0.80%HHx(3-羟基己酸);以20%丁酸钠和80%1,4-丁二醇培养活性污泥所得到的PHAs含有与3#样品相同的七种单体,只是比例不同,分别是61.39mol%,23.01mol%,4.58mol%,5.97mol%,0.91mol%,2.37mol%,1.77mol%;以60%戊酸钠和40%葡萄糖培养活性污泥所得到的PHAs由HB和HV组成,比例是41.24 mol%∶58.76 mol%;以60%苯甲酸钠和40%葡萄糖培养活性污泥所得到的PHAs也由HB和HV组成,比例是65.48 mol%∶34.52 mol%。

Coconut oil is an excellent emollient, being a rich source of saturated fatty acids like oleic acid, linoleic acid, lauric acid, capric acid, caprylic acid, myristic acid and palmitic acid.

椰子油是一个很好的润肤,身为如油酸饱和脂肪酸的丰富来源,亚油酸,月桂酸,癸酸,辛酸,肉豆蔻酸,棕榈酸。

First, a lot of experiments about changing character on CaCO3 surface has been rearsched,example,fatty acid,pentaerythritol,rosin ester,cocoanut oil,rosin, pentaerythritol + rosin ester,glycerine + rosin ester ,cocoanut oil + oleic acid,titanate + fatty acid,cocoanut oil + fatty acid, and so on surface active agents. Among these surface active agents, cocoanut oil + oleic acid,and titanate+ fatty acid,and cocoanut oil + fatty acid are the best.

本文首先对纳米碳酸钙的活化改性进行了实验研究,在硬脂酸钠、季戊四醇、松香酯、椰子油、松香、季戊四醇+松香酯、甘油+松香酯、椰子油+油酸、钛酸酯+硬脂酸钠、椰子油+硬脂酸钠等表面改性剂中,以硬脂酸钠、椰子油、油酸+椰子油、椰子油+硬脂酸钠等活化剂的活化效果较为理想。

The present invention adopts the technical proposal of adopting ZSM-5 mesoporous molecular sieve raw powder with a silicon-aluminum mol ratio SiO2Al2O3 of 20 to 1000 and a weight percentage of 20 to 100 percent as well as at least one caking agent selected from SiO2, clay and Al2O3 to extrude, tablet or spray into shape; then treating for 1 to 8 hours by 0.1 to 3 mol/l of at least one ammonium liquor from ammonium nitrate, ammonium chloride or ammonium sulphate or 0.1 to 8.5 mol/l of at least one acid liquor from muriatic acid, nitric acid, vitriol or acetic acid under a temperature of 20 to 90 DEG C; then using steam to treat for 2 to 15 hours under the temperature condition of 400 to 700 DEG C; using a liquor of 0.1 to 3mol/l selected from at least one of oxalic acid, citric acid or maleic acid under a temperature condition of 20 to 90 DEG C to dip for 2 to 5 hours to obtain the modified molecular sieve catalyst, thus better solving the problems.

本发明通过采用硅铝比SiO2/Al2O3为20~1000重量百分比计20~100%的ZSM-5介孔分子筛原粉与余量的选自SiO2、粘土或Al2O3中至少一种粘结剂挤条、压片或喷球成型;再经过0.1~3摩尔/升选自硝酸铵、氯化铵或硫酸铵中的至少一种铵溶液或0.1~8.5摩尔/升选自盐酸、硝酸、硫酸或乙酸中的至少一种酸溶液在温度20~90℃下处理1~8小时;然后在温度为400~700℃条件下水蒸汽处理2~15小时;再用0.1~3摩尔/升选自草酸、柠檬酸或马来酸中至少一种在温度为20~90℃条件下浸渍2~5小时得所需改性分子筛催化剂的技术方案较好地解决了该问题,可用于甲醇转化制丙烯的工业生产中。

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