本文研究了山药苯丙氨酸解氨酶(PAL)的动力学特性。
The kinetic characteristics of phenylalanine ammonia-lyase (PAL) in yam was studied.
用固体加入法研究了银杏叶苯丙氨酸解氨酶（PAL）的盐析过程。
The course of salting-out the phenylalanine ammonia-lyase(PAL) in Ginkgobiloba leaves was studied.
这些病毒显示没有与包括奥斯他韦(达菲)在内的神经氨酶抑制剂耐药性有关的突变。
The viruses showed no mutations associated with resistance to the neuraminidase inhibitors, including oseltamivir (Tamiflu).
苯丙氨酸解氨酶(PAL)生物转化肉桂酸生产L苯丙氨酸成了该领域研究与开发的热点。
The biotransformation of trans-cinnamic acid to L-phenylalanine by using phenylalanine ammonia-lyase (PAL) has, therefore, become very important in the research and development of this field.
与抗病性相关酶类的活性，如苯丙氨酸解氨酶（PAL）、多酚氧化酶（PPO）活性均高于对照。
The activity of resistance-related enzymes, such as phenylalanine ammonia-lyase (PAL), polyphenol oxidase (PPO) and peroxidase (POD) were higher than that of control.
苯丙氨酸解氨酶的株间差异相对较小，但在总体水平上，抗病无性系的酶活性和比活性也比易感株略高。
Phenylalanine ammonia lyase activities of the resistant clone needles, in general, were also a bit higher than those of susceptible individuals.
例如苯丙氨酸解氨酶（PAL）、过氧化物酶（POD）、多酚氧化酶（PPO），这些酶和植物的抗病性是密切相关的。
Such as PAL, POD , SOD and PPO , which are strongly associated with the plant disease resistance.
目的研究联合检测甘氨酰脯氨酸二肽氨基肽酶（GPDA）及其同工酶、腺苷脱氨酶（ADA）对不同性质腹水的鉴别诊断价值。
Objective To study the value of GPDA and its isoenzymes as well as ADA in the differential diagnosis of ascites.
不同时期叶面喷施硼酸降低了梨果石细胞含量，果实过氧化物酶、多酚氧化酶和苯丙氨酸解氨酶活性也低于对照，且幼果期处理效果最佳。
The contents of sclereid and activities of some enzymes, such as POD, PPO and PAL are decreased under the applications of H3BO3, and the effect of the application at young fruit stage is the best.
苯丙氨酸解氨酶（PAL）主要分布在果皮中，并随着果实成熟度的提高，其活性呈极显著下降趋势。感病果实的果皮中三种酶活性均比健康果皮高。
Phenylalanine ammonia-lyase (PAL) is distributed mainly in the peels, and activity of the enzymes decreased very obviously with the increase of fruit ripeness.
结果表明，喷施水杨酸抑制了过氧化物酶（POD）、多酚氧化酶（PPO）、苯丙氨酸解氨酶（PAL）活性，降低了石细胞的大小、密度和含量。
The results showed that POD, PPO and PAL activities were inhibited and the stone cell density , diameter and contents were decreased in the treatment of SA spraying;
通过不同浓度和不同诱导时间两种处理方式，测定了壳低聚糖和L - C对黄瓜叶片中过氧化物酶、多酚氧化酶和苯丙氨酸解氨酶等防御酶的诱导效果。
Activities of the defense enzymes involved in POD, PPO and PAL induced by COS and L-C were measured by two different treatments of different concentrations and different induced time.
针对苯丙氨酸解氨酶生物传感器非线性特性，依据最小二乘法理论，采用最优化技术，建立了最佳拟合直线的数学模型，并给出基于可编程控制器的数据拟合程序。
To solve the non-linear problem of a biosensor, the least square method and the optimum technique have been applied to build a mathematical model to evaluate the optimum fitting straight.
这些发现提供了利用药物来阻碍门冬氨酰蛋白酶发挥作用的可能性。
The findings open the possibility of using drugs to block the action of plasmepsin V.
这些作物都能产生一种名为钒固氮(vanadium nitrogenase)的酶，它具有把氮转变成氨的能力。
It creates an enzyme called vanadium nitrogenase, which produces ammonia from nitrogen.
铜是人体必需的微量元素之一，是胎膜中胶原纤维发育成熟的关键酶赖氨酰氧化酶的活性辅基。
Copper is one of essential trace elements for human, acting as an active agon of lysyloxidase which is critical enzyme for collagen maturation.
虽然这些产氨菌不能有效地降解蛋白质，但它们可以利用其他瘤胃细菌的蛋白酶或肽酶水解的产物小肽与氨基酸。
Although these ammonia producers have limited ability to degrade proteins, they can utilize peptides or amino acids released by the proteases and peptidases of other ruminal bacteria.
综述了青霉素乙酰化固定化酶和头孢氨苄酶法缩合工艺的研究进展；
The advances in immobilized acetylase of penicillin and process of enzymatic condensation in cephalexin synthesis were reviewed.
氨基糖苷类抗生素的修饰酶是细菌耐药的主要机制，本文对氨糖类抗生素的修饰酶抑制剂的研究进展作一综述。
Aminoglycoside modifying enzyme is the main resistance mechanism. In this review, some advances in the research of aminoglycoside modifying enzyme inhibitor are summarized.
用基于线性响应近似的自由能预测方法计算胰蛋白酶和苯酰氨类抑制剂的结合自由能。
Binding affinities of a series of benzamide inhibitors for trypsin were evaluated by molecular dynamics (MD) simulations using a linear response approach.
综述了酶法合成头孢氨苄的工艺方法研究进展。
The advances in the process technology for the enzymatic synthesis of cephalexin are reviewed.
目的：为了解人肝癌组织及血清中甘氨酰脯氨酸二肽氨基肽酶(GPDA)同工酶变化，探讨其临床意义。
Objective: To study changes of GPDA isoenzyme in serum and hepatic tissues in patients with primary hepatic carcinoma and explore the clinical significance.
结果：左旋氨氯地平可以降低心肌酶的活性，减轻缺血造成的心肌细胞损伤程度。
The results showed that L-Amlodipine can reduce the ultrastructural injuries of myocardium and diminish the myocardial enzyme activity of blood serum.
本文采用基于线性响应近似的自由能预测方法计算了胰蛋白酶和苯酰氨类抑制剂的结合自由能。
The binding affinities of a series of benzamide inhibitors with trypsin were evaluated by molecular dynamics (MD) simulations with a linear response approach.
来源于巨大芽孢杆菌的固定化酶催化头孢克罗合成的能力较好，以苯甘氨酸甲酯（PGME）为底物较酰氨的效果好。
The immobilized enzyme from Bacillis megaterium gave a better catalytic properties and the higher conversion was obtained using phenylglycine methyl ester (PGME) as acyl donor.
细胞内鞘氨醇激酶（SPK）是催化鞘氨醇生成1-磷酸鞘氨醇（S1P）的限速酶。
Sphingosine kinase (SPK) is a key enzyme catalyzing the formation of sphingosine 1 phosphate (S1P), which is a lipid messenger with strong angiogenic activity.
选用巯基酶的专一性抑制剂—碘乙酰氨对白地霉原生质体进行灭活处理。
Choosing the specific depressor of mercapto-iodoacetamide (IAM) to destroy the geotrichum candidium of protoplast.
这一抗原决定簇对神经氨(糖)酸苷酶敏感，但对蛋白酶不敏感。
This epitope is sensitive to neuraminidase, but insensitive to protease.
这一抗原决定簇对神经氨(糖)酸苷酶敏感，但对蛋白酶不敏感。
This epitope is sensitive to neuraminidase, but insensitive to protease.
应用推荐