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质量水平
检测方案
≥98% (TLC)
形式
powder
技术
ligand binding assay: suitable
颜色
white to off-white
mp
215 °C (dec.) (lit.)
溶解性
H2O: soluble
SMILES字符串
NCCCC[C@H](N)C(O)=O
InChI
1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m0/s1
InChI key
KDXKERNSBIXSRK-YFKPBYRVSA-N
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一般描述
L-赖氨酸含有碱性侧链，是亲水性的。其侧链上的正丁基氨基在生理pH值下被质子化。降解后，L-赖氨酸产生酮体。赖氨酸与α-酮戊二酸酯的转胺反应生成乙酰乙酰辅酶A。L-赖氨酸作为次生代谢产物的前体，如β-内酰胺抗生素。它也是合成α-氨基己二酸的前驱体。
应用
L-赖氨酸是一种必需的蛋白原α氨基酸，其广泛用于各种应用。它已被用作：
- 细胞培养基的一种补充物
- 以L-赖氨酸氧化酶(EC 1.4.3.14)等酶为底物
- 作为多聚赖氨酸聚合物的组分
- 作为聚赖氨酸聚合物的组成部分
- 作为底物进行氧化和糖基化机理研究在钴赖氨酸的制备中
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
A L Leitão et al.
Applied microbiology and biotechnology, 56(5-6), 670-675 (2001-10-17)
In beta-lactam producing microorganisms, the first step in the biosynthesis of the beta-lactam ring is the condensation of three amino acid precursors: alpha-aminoadipate, L-cysteine and D-valine. In Nocardia lactamdurans and other cephamycin-producing actinomycetes, alpha-aminoadipate is generated from L-lysine by two
S P Collin
The Journal of comparative neurology, 281(1), 143-158 (1989-03-01)
The retinal topography of the adult coral trout Plectropoma leopardus (Serranidae, Perciformes) is examined in Nissl-stained material and confirmed by means of retrograde labelling with cobalt-lysine from the optic nerve. Concentric isodensity contours surround a temporoventral area centralis of over
Devlin T M
Textbook of Biochemistry: With Clinical Correlations (5th ed.), 97-97 (2002)
A D Springer et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 30(12), 1235-1242 (1982-12-01)
The introduction of heavy metals directly into living neuronal tissue has received little attention as a method for defining connections in the vertebrate nervous system. Procedures are described for the use of cobaltous-lysine to trace visual pathways with light microscopy.
François-Michel Boisvert et al.
Molecular & cellular proteomics : MCP, 11(3), M111-M111 (2011-09-23)
Measuring the properties of endogenous cell proteins, such as expression level, subcellular localization, and turnover rates, on a whole proteome level remains a major challenge in the postgenome era. Quantitative methods for measuring mRNA expression do not reliably predict corresponding
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