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甘氨酸

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The glycine solution has more competitive nucleating ability in higher initial temperature as 30 and 35℃,and less competitive nucleating ability in lower initial temperature as 20 and 25℃.

甘氨酸饱和溶液在较高起始温度30和35℃下成核能力较差,在较低起始温度20和25℃下成核能力较强。

With futher increasing ethanol content in mixedsolvent, the repulsing interactions decrease, the attracting interactionsbecome mainly and increase between L-valine molecules.

随乙醇含量的增大,甘氨酸两分子间偶极吸引作用在25%乙醇水溶液中最大;L-丝氨酸羟基的吸引作用在25%乙醇水溶液中也出现极大值。

A 100mL solution of 0.1 M giycine at pH 1.72 was titrated with 2 M NaOH solution.

100mL的0.1M的甘氨酸在pH1.72时用2M的NaOH滴定。

Contains Glycine, an amino acid that works in conjunction with collagen to promote skin moisturization.

包含甘氨酸,一种与胶原共同作用的氨基酸来促进皮肤保湿。

Nanocrystalline ZnO was prepared by the combustion synthesis method for the first time.

首次以硝酸锌和甘氨酸为原料,用燃烧合成法制备了纳米ZnO粉体。

In the third part, MP2 and B3LYP methods are employed to study the relative stabilities of conformers of N-Cl glycine using 6-311 G** basis set.

第三部分采用了MP2和B3LYP方法在6-311 G**基组水平下研究了13种N-Cl甘氨酸异构体的相对稳定性。

Methods: Fat extracted from food and oil sample was determined directly on the ZnSe crystal cisterna of horizon attenuation total reflection equipment with deuterated triglycine sulfate detector in the FT-IR.

食品中提取的脂肪或油脂样品直接置于红外光谱仪的水平衰减全反射部件的槽式ZnSe晶体上,氘化三甘氨酸硫酸酯检测器检测。

Several underivatized HPLC methods for analysing and separating the system is explored, through which serine can be gotten after the reaction of glycin with formaldehyde .

对于甘氨酸和甲醛反应制备丝氨酸的反应体系,试验了几种非衍生化的高效液相色谱分析方法。

When LA, glycin and succinate were added, ALA production of strain 99-28 was significantly increased whereas the CODcr removal was ad-versely affected.

废水不灭菌略微降低99-28菌株的生长和CODcr的去除能力,在添加LA、甘氨酸和琥珀酸的条件下的,ALA产量明显下降。

Then, they were transferred into the mycelium culture fluid which includes 30% sucrose and 1% or 1.5% glycin under the condition of 20℃, 150 rpm for 48 h. In order to obtain protoplasts of mass and high quality, the strain F46 protoplasts given after combination use of the 10 mg·mL-1 lysozyme and 10 mg·mL-1 snailase at 34℃for 3 h; and the SC1 was treated by 10 mg·mL-1 lysozyme at 34℃for 2.5 h.

确定了双亲原生质体形成与再生的最佳条件:菌株F46、SC1采用二次菌丝培养,即在蔗糖含量20%菌丝培养液里,25℃条件下150 rpm培养48 h;然后按15%的接种量转接到蔗糖含量30%,甘氨酸含量分别为1%、1.5%的菌丝培养液中,同样条件下,继续培养48 h;在34℃条件下,菌株F46用等量混合的蜗牛酶和溶菌酶20 mg·mL-1,菌株SC1用10 mg·mL-1溶菌酶,分别酶解3 h、2.5 h,不仅有大量的原生质体形成,且再生率也高。

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