结晶紫

Actinobacteria retain the deep purple color of crystal violet; Gram negative bacteria (e.g. Cyanobacteria) are decolorized, and may be counterstained with other dyes, such as safranin, carbol fuchsin, neutral red.

革兰氏阳性菌会保持结晶紫的深紫红色；革兰氏阴性菌则会褪色，但可以被其他染料复染，如碱性藏红、品红或中性红。

VIS-UV-spectra show that Spirulina subsalsa is able to degrade these three kinds of dyes when the solution containing 5 mgL^(-1) crystal violet, 5 mgL^(-1) safranine T, and 15 mgL^(-1) methylene blue, respectively.

经紫外光谱分析，当结晶紫、番红花红T的浓度为5mgL^(-1)和亚甲基兰浓度为15mgL^(-1)时，盐泽螺旋藻对这三种染料都存在降解作用。

Three new-type charge-transfer salts were synthesized based on the reaction of three kinds of basic dye (crystal violet, safranine T, methylene blue BB, respectively) and tungstophosphoric acid of Keggin structure.

报道了用Keggin结构的磷钨酸与碱性染料结晶紫、碱性藏红T和碱性湖兰BB反应形成的3种新型电荷转移盐。

The sample was dissolved by hydrofluoric acid and hydrogen nitrate, then the tantalite and hydrofluoric acid formed TaF6- in the media of tartaric acid－hydrofluoric acid.

试样以氢氟酸、硝酸溶解后，在酒石酸－氢氟酸介质中，钽酸与氢氟酸形成阴离子TaF6-，与结晶紫生成蓝紫色的络合物，用苯萃取出来采用光度法测定钽量，测定结果均在国标允许误差范围内。

Methods: Triphenylmethane dyes MG and CV respectively react with some negative ions under suitable conditions to form a hydrophobic ion-associate.

孔雀石绿和结晶紫都是三苯甲烷类阳离子染料，在一定条件下，将其与大阴离子反应，形成离子缔合物而失去亲水性。

Among these strains, Bjerkandera adusta Y5012, Cerrena unicolor Y5002, Funalia trogii Y4997, Trametes suaveolens D8325 and Trametes versicolor Y4946 showed stronger capacity to decolorize the 6 different dyes. The factors related to decolorization of orange G and alizarin red of strain Cerrena unicolor Y5002 were studied by the method of shaking flask.

在40株菌株中，黑管孔菌Bjerkandera adusta Y5012，一色齿毛菌Cerrena unicolor Y5002，硬毛粗盖孔菌Funalia trogii Y4997，香栓孔菌Trametes suaveolens D8325和云芝栓孔菌Trametes versicolor Y4946对刚果红、橙黄G、茜素红、结晶紫、中性红和亚甲基蓝均显示出较强的脱色能力。

The preparation and operation of automatic sampling instrument, the selections of light reported andmeasurement way are described in betail in the paper.

文中详细叙述了自动进液装置的制作，使用方法，光源及测量方式的选择，试验确定了Au－溴－结晶紫离子缔合物萃取显色体系的最佳分析条件。

Leuco crystal violet lactone was prepared by heating the mixture of dimethylaniline, p- dimethylaminobenzaldehyde and m- dimethylaminobenzoic acid at 60 ℃ for 5 hours in presence of hydrochioric acid and unea and in the nitrogen atmosphere with 72% yield of LCVL.

等摩尔比的N，N-二甲基苯胺和对二甲氨基苯甲醛在盐酸和脲的存在及氮气保护下，80℃反应0.5h，加入间二甲氨基苯甲酸于90℃反应5h。将反应混合物中和，抽滤，得到无色结晶紫内酯，产率为72%。

Leuco crystal violet lactone was prepared by heating the mixture of dimethylaniline, p-dimethylaminobenzaldehyde and m-dimethylaminobenzoic acid at 60℃ for 5 hours in presence of hydrochloric acid and urea and in the nitrogen atmosphere with 72%yield of LCVL.

等摩尔比的N，N-二甲基苯胺和对二甲氨基苯甲醛在盐酸和脲的存在及氮气保护下，80℃反应0.5h，加入间二甲氨基苯甲酸于90℃反应5h。将反应混合物中和，抽滤，得到无色结晶紫内酯，产率为72%。

In this study, different nano-hydroxyapatite particles,HAP_1(25-60nm), HAP_4(the additives is heparin, 15-50nm), HAP_5(the additives is bovine serum albumin BSA, 20-80nm) were prepared by homogeneous precipitation and used heavy-gauge hydroxyapatite as comparison,we determined amount of heparin, sialic acid ,BSA adsorbed on HAP_1,HAP_2,HAP_3 by Crystal Violet assay, Bialsche method,Bradford method respectively and analyzed the binding mechanism by infrared spectrum;After taking HAP_1,HAP_2,HAP_4,HAP_5 and RBC to co-culture in vitro,we studied RBC hemolysis test and detected RBC hematolysis rate by erythrocyte osmotic fragility test;observing the changes of morphous and locomotion of cell after coacting HAP_1,HAP_2,HAP_4,HAP_5 and RBC by light microscope and inverted phase contrast microscope;observing HAP_1,HAP_2,HAP_4,HAP_5 effecting on Ultrastructure of RBC.

本文用均匀沉淀法制备了HAP_1(25-60nm)，HAP_4(添加剂肝素，15-50nm)，HAP_5(添加剂牛血清白蛋白BSA，20-80nm)等纳米粒子，并用大尺寸的羟基磷灰石HAP_2(470-520nm)，HAP_3(1906nm)作对照，分别利用结晶紫法、Bialsche法、Bradford法研究了肝素、唾液酸、血清白蛋白在HAP_1，HAP_2，HAP_3上的吸附量，用红外光谱分析其中的结合机理；在体外将HAP_1，HAP_2，HAP4_，HAP_5与红细胞共培养，进行了红细胞溶血试验的研究，并借助红细胞渗透脆性试验检测红细胞溶血率；运用普通光学显微镜和倒置相差显微镜观察了HAP_1，HAP_2，HAP_4，HAP_5与红细胞作用后细胞形态及运动的变化：透射电镜观察了HAP_1，HAP_2，HAP_4，HAP_5对红细胞超微结构的影响。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。