Cadaverine (BioDeep_00000003107)
Secondary id: BioDeep_00000400193
natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019
代谢物信息卡片
Pentamethylenediamine dihydrochloride
化学式: C5H14N2 (102.1156924)
中文名称: 1,5-二氨基戊烷, 尸胺 二盐酸盐, 尸胺
谱图信息:
最多检出来源 Homo sapiens(feces) 0.34%
分子结构信息
SMILES: C(CCN)CCN
InChI: InChI=1/C5H14N2/c6-4-2-1-3-5-7/h1-7H2
描述信息
Cadaverine is a foul-smelling diamine formed by bacterial decarboxylation of lysine that occurs during protein hydrolysis during putrefaction of animal tissue. However, this diamine is not purely associated with putrefaction. It is also produced in small quantities by mammals. In particular, it is partially responsible for the distinctive smell of urine and semen. Elevated levels of cadaverine have been found in the urine of some patients with defects in lysine metabolism. Cadaverine is toxic in large doses. In rats it had a low acute oral toxicity of more than 2000 mg/kg body weight .; Cadaverine is a foul-smelling molecule produced by protein hydrolysis during putrefaction of animal tissue. Cadaverine is a toxic diamine with the formula NH2(CH2)5NH2, which is similar to putrescine. Cadaverine is also known by the names 1,5-pentanediamine and pentamethylenediamine.
Cadaverine is a foul-smelling diamine formed by bacterial decarboxylation of lysine that occurs during protein hydrolysis during putrefaction of animal tissue. However, this diamine is not purely associated with putrefaction. Cadaverine is a toxic diamine with the formula NH2(CH2)5NH2, which is similar to putrescines NH2(CH2)4NH2. Cadaverine is also known by the names 1,5-pentanediamine and pentamethylenediamine. It is also produced in small quantities by mammals. In particular, it is partially responsible for the distinctive smell of urine and semen. Elevated levels of cadaverine have been found in the urine of some patients with defects in lysine metabolism. Cadaverine is toxic in large doses. In rats it had a low acute oral toxicity of more than 2000 mg/kg body weight. Cadaverine can be found in Corynebacterium (PMID:27872963).
Acquisition and generation of the data is financially supported in part by CREST/JST.
C78272 - Agent Affecting Nervous System > C66880 - Anticholinergic Agent
KEIO_ID C032
同义名列表
15 个代谢物同义名
Pentamethylenediamine dihydrochloride; 1,5-Diaminopentane dihydrochloride; cadaverine dihydrochloride; 1,5-Pentamethylenediamine; Pentamethylenediamine; Pentane-1,5-diamine; 1,5-Diaminopentane; 1,5 Pentanediamine; 1,5-Pentanediamine; Cadaverine; Cadaverin; BioDex 1; DAPE; Cadaverine; Cadaverine
数据库引用编号
34 个数据库交叉引用编号
- ChEBI: CHEBI:18127
- KEGG: C01672
- PubChem: 273
- HMDB: HMDB0002322
- Metlin: METLIN3236
- DrugBank: DB03854
- ChEMBL: CHEMBL119296
- Wikipedia: Cadaverine
- MeSH: Cadaverine
- MetaCyc: CADAVERINE
- KNApSAcK: C00001403
- foodb: FDB001493
- chemspider: 13866593
- CAS: 462-94-2
- MoNA: KO002542
- MoNA: PR100024
- MoNA: KO002544
- MoNA: PS004401
- MoNA: PS004402
- MoNA: KO002546
- MoNA: KO002543
- MoNA: KO002545
- PMhub: MS000008081
- PubChem: 4816
- PDB-CCD: LB9
- PDB-CCD: N2P
- 3DMET: B00334
- NIKKAJI: J5.771A
- RefMet: Cadaverine
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-354
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-796
- KNApSAcK: 18127
- LOTUS: LTS0046069
- wikidata: Q161555
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
288 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(6)
- aminopropylcadaverine biosynthesis:
H+ + lys ⟶ CO2 + cadaverine - superpathway of polyamine biosynthesis I:
H2O + agmatine ⟶ putrescine + urea - superpathway of polyamine biosynthesis I:
H2O + agmatine ⟶ putrescine + urea - superpathway of arginine and polyamine biosynthesis:
N-acetyl-L-ornithine + H2O ⟶ L-ornithine + acetate - aminopropylcadaverine biosynthesis:
S-adenosyl-L-methioninamine + cadaverine ⟶ S-methyl-5'-thioadenosine + H+ + aminopropylcadaverine - lysine degradation I:
H+ + L-lysine ⟶ CO2 + cadaverine
WikiPathways(0)
Plant Reactome(276)
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
H2O + L-Asn ⟶ L-Asp + ammonia - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid metabolism:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
2OG + L-Val ⟶ Glu + KIV - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
H2O + L-Asn ⟶ L-Asp + ammonia - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
H2O + L-Asn ⟶ L-Asp + ammonia - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + KIV + NAD ⟶ ISB-CoA + NADH + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid metabolism:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA - Amino acid metabolism:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide - Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid metabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Amino acid catabolism:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide - Lysine degradation I:
L-Lys ⟶ cadaverine + carbon dioxide
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(6)
- Aminopropylcadaverine Biosynthesis:
Hydrogen Ion + L-Lysine ⟶ Cadaverine + Carbon dioxide - Aminopropylcadaverine Biosynthesis:
Hydrogen Ion + L-Lysine ⟶ Cadaverine + Carbon dioxide - Lysine Degradation I:
Hydrogen Ion + L-Lysine ⟶ Cadaverine + Carbon dioxide - Lysine Metabolism:
Hydrogen Ion + meso-diaminopimelate ⟶ Carbon dioxide + L-Lysine - Lysine Degradation I:
Hydrogen Ion + L-Lysine ⟶ Cadaverine + Carbon dioxide - Tropane, Piperidine, and Pyridine Alkaloid Biosynthesis:
Hydrogen Ion + N-Methylputrescine + Oxygen ⟶ 1-Methylpyrrolinium + Ammonia + Hydrogen peroxide
PharmGKB(0)
42 个相关的物种来源信息
- 3702 - Arabidopsis thaliana: 10.1186/S12864-017-4381-3
- 182803 - Araneus ventricosus: 10.1016/0305-0491(91)90393-R
- 4424 - Brasenia schreberi: 10.1139/B97-175
- 41689 - Brugmansia arborea: 10.1016/S0031-9422(01)00127-3
- 3824 - Canavalia gladiata: 10.1016/0031-9422(90)85449-P
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 3827 - Cicer arietinum: 10.1016/0031-9422(92)83265-Z
- 34814 - Coryphaena hippurus: 10.1021/JF020148X
- 35525 - Daphnia magna: 10.1016/J.ENVINT.2009.12.006
- 3847 - Glycine max:
- 168338 - Heliotropium angiospermum: 10.1016/S0031-9422(00)82598-4
- 368676 - Hippobroma longiflora: 10.1021/NP800743W
- 9606 - Homo sapiens: -
- 55464 - Hydrocharis morsus-ranae: 10.1016/S0031-9422(00)80829-8
- 72129 - Hypholoma fasciculare: 10.1055/S-0028-1097581
- 3860 - Lathyrus sativus: 10.1016/0031-9422(74)85020-X
- 308559 - Lobelia inflata: 10.1021/NP800743W
- 330173 - Lobelia siphilitica: 10.1021/NP800743W
- 3870 - Lupinus albus:
- 3871 - Lupinus angustifolius: 10.1016/S0021-9258(17)40759-9
- 3872 - Lupinus arboreus: 10.1016/S0021-9258(17)40759-9
- 53238 - Lupinus bicolor: 10.1016/S0021-9258(17)40759-9
- 53225 - Lupinus digitatus: 10.1016/S0021-9258(17)40759-9
- 3873 - Lupinus luteus:
- 53230 - Lupinus micranthus: 10.1016/S0021-9258(17)40759-9
- 53232 - Lupinus mutabilis: 10.1016/S0021-9258(17)40759-9
- 53237 - Lupinus pilosus: 10.1016/S0021-9258(17)40759-9
- 3874 - Lupinus polyphyllus: 10.1016/S0021-9258(17)40759-9
- 442941 - Lyallia kerguelensis: 10.1016/S0031-9422(99)00191-0
- 73626 - Lycopodiastrum casuarinoides:
- 4087 - Nicotiana alata: 10.1016/0031-9422(84)83018-6
- 73621 - Palhinhaea cernua: 10.1016/J.PHYTOCHEM.2016.08.010
- 49511 - Piper longum:
- 13216 - Piper nigrum:
- 1595995 - Piper trichostachyon:
- 3888 - Pisum sativum: 10.1016/0031-9422(90)85450-T
- 286 - Pseudomonas: 10.2323/JGAM.37.431
- 3891 - Psophocarpus tetragonolobus: 10.1016/0031-9422(90)85450-T
- 28893 - Streptomyces pilosus: 10.1186/1475-2859-2-5
- 22666 - Trapa natans: 10.1139/B97-175
- 192294 - Utricularia intermedia: 10.1016/S0031-9422(00)80829-8
- 29760 - Vitis vinifera:
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
文献列表
- Serkan Ozmen, Selma Tabur, Signem Oney-Birol. Alleviation role of exogenous cadaverine on cell cycle, endogenous polyamines amounts and biochemical enzyme changes in barley seedlings under drought stress.
Scientific reports.
2023 10; 13(1):17488. doi:
10.1038/s41598-023-44795-z. [PMID: 37840053] - Chen Chen, Jun Chen, Guangxi Wu, Liling Li, Zhangli Hu, Xiaozheng Li. A Blue Light-Responsive Strong Synthetic Promoter Based on Rational Design in Chlamydomonas reinhardtii.
International journal of molecular sciences.
2023 Sep; 24(19):. doi:
10.3390/ijms241914596. [PMID: 37834043] - Dujun Wang, Li Zhao, Jingqiong Wan, Jia Liu, Yuan Wei, Zhen Ouyang, Xiaohong Yu. Molecular cloning, expression, and functional analysis of copper amine oxidase gene from mulberry (Morus alba L.).
Protein expression and purification.
2023 01; 201(?):106166. doi:
10.1016/j.pep.2022.106166. [PMID: 36174814] - Robert A Freudenberg, Luisa Wittemeier, Alexander Einhaus, Thomas Baier, Olaf Kruse. Advanced pathway engineering for phototrophic putrescine production.
Plant biotechnology journal.
2022 10; 20(10):1968-1982. doi:
10.1111/pbi.13879. [PMID: 35748533] - Yangyang Yu, Lu Li, Yujuan Xu, Kejing An, Qiao Shi, Yuanshan Yu, Zhenlin Xu. Evaluation of the Relationship among Biogenic Amines, Nitrite and Microbial Diversity in Fermented Mustard.
Molecules (Basel, Switzerland).
2021 Oct; 26(20):. doi:
10.3390/molecules26206173. [PMID: 34684752] - Nicole M Gibbs, Shih-Heng Su, Samuel Lopez-Nieves, Stéphane Mann, Claude Alban, Hiroshi A Maeda, Patrick H Masson. Cadaverine regulates biotin synthesis to modulate primary root growth in Arabidopsis.
The Plant journal : for cell and molecular biology.
2021 09; 107(5):1283-1298. doi:
10.1111/tpj.15417. [PMID: 34250670] - Leonie Verhage. Smelly business - Cadaverine modulates root growth by inhibiting biotin synthesis.
The Plant journal : for cell and molecular biology.
2021 09; 107(5):1281-1282. doi:
10.1111/tpj.15471. [PMID: 34535941] - Sophie Maiocchi, Jacqueline Ku, Tom Hawtrey, Irene De Silvestro, Ernst Malle, Martin Rees, Shane R Thomas, Jonathan C Morris. Polyamine-Conjugated Nitroxides Are Efficacious Inhibitors of Oxidative Reactions Catalyzed by Endothelial-Localized Myeloperoxidase.
Chemical research in toxicology.
2021 06; 34(6):1681-1692. doi:
10.1021/acs.chemrestox.1c00094. [PMID: 34085520] - Mohsin Amin, Shiying Tang, Liliana Shalamanova, Rebecca L Taylor, Stephen Wylie, Badr M Abdullah, Kathryn A Whitehead. Polyamine biomarkers as indicators of human disease.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.
2021 Mar; 26(2):77-94. doi:
10.1080/1354750x.2021.1875506. [PMID: 33439737] - Saima Ameen Ghoto, Muhammad Yar Khuhawar. Silver Nanoparticles for a Colorimetric Determination of Putrescine and Cadaverine in Biological Samples.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.
2021 Feb; 37(2):267-274. doi:
10.2116/analsci.20p153. [PMID: 32779576] - Benjamin P Heithoff, Kijana K George, Aubrey N Phares, Ivan A Zuidhoek, Carmen Munoz-Ballester, Stefanie Robel. Astrocytes are necessary for blood-brain barrier maintenance in the adult mouse brain.
Glia.
2021 02; 69(2):436-472. doi:
10.1002/glia.23908. [PMID: 32955153] - Xiya Zhang, Xijie Zhang, Lianjun Song, Xianqing Huang, Yu Li, Mingwu Qiao, Wanjing Liu, Tongtong Zhang, Yuchen Qi, Wuzhou Wang, Xuezhi Yu, Leina Dou, Huijuan Yang, Liye Wang, Yexuan Mao, Zhanhui Wang. An ultrasensitive, homogeneous fluorescence quenching immunoassay integrating separation and detection of aflatoxin M1 based on magnetic graphene composites.
Mikrochimica acta.
2021 01; 188(2):59. doi:
10.1007/s00604-021-04715-2. [PMID: 33507410] - Kay Diederen, Jia V Li, Gillian E Donachie, Tim G de Meij, Dirk R de Waart, Theodorus B M Hakvoort, Angelika Kindermann, Josef Wagner, Victoria Auyeung, Anje A Te Velde, Sigrid E M Heinsbroek, Marc A Benninga, James Kinross, Alan W Walker, Wouter J de Jonge, Jurgen Seppen. Exclusive enteral nutrition mediates gut microbial and metabolic changes that are associated with remission in children with Crohn's disease.
Scientific reports.
2020 11; 10(1):18879. doi:
10.1038/s41598-020-75306-z. [PMID: 33144591] - Changxin Liu, Kostadin E Atanasov, Nazanin Arafaty, Ester Murillo, Antonio F Tiburcio, Jürgen Zeier, Rubén Alcázar. Putrescine elicits ROS-dependent activation of the salicylic acid pathway in Arabidopsis thaliana.
Plant, cell & environment.
2020 11; 43(11):2755-2768. doi:
10.1111/pce.13874. [PMID: 32839979] - Thomas Boehm, Matthias Karer, Elisabeth Gludovacz, Karin Petroczi, Marlene Resch, Kornelia Schuetzenberger, Kristaps Klavins, Nicole Borth, Bernd Jilma. Simple, sensitive and specific quantification of diamine oxidase activity in complex matrices using newly discovered fluorophores derived from natural substrates.
Inflammation research : official journal of the European Histamine Research Society ... [et al.].
2020 Sep; 69(9):937-950. doi:
10.1007/s00011-020-01359-5. [PMID: 32488317] - Scarlett Puebla-Barragan, Justin Renaud, Mark Sumarah, Gregor Reid. Malodorous biogenic amines in Escherichia coli-caused urinary tract infections in women-a metabolomics approach.
Scientific reports.
2020 06; 10(1):9703. doi:
10.1038/s41598-020-66662-x. [PMID: 32546787] - Lawrence M Schopfer, Oksana Lockridge. Signature Ions in MS/MS Spectra for Dansyl-Aminohexyl-QQIV Adducts on Lysine.
Molecules (Basel, Switzerland).
2020 Jun; 25(11):. doi:
10.3390/molecules25112659. [PMID: 32521655] - Min-Ling Zheng, Liang-Hui Li, Bin Liu, Yu-Bo Lin, Xiao-Tuan Zhang, Cha Chen, Ping-Hua Qu, Jian Zeng. Haemophilus seminalis sp. nov., isolated from human semen.
International journal of systematic and evolutionary microbiology.
2020 Apr; 70(4):2588-2595. doi:
10.1099/ijsem.0.004074. [PMID: 32163029] - Vivek Ambastha, Yael Friedmann, Yehoram Leshem. Laterals take it better - Emerging and young lateral roots survive lethal salinity longer than the primary root in Arabidopsis.
Scientific reports.
2020 02; 10(1):3291. doi:
10.1038/s41598-020-60163-7. [PMID: 32094490] - Iris Samarra, Bruno Ramos-Molina, M Isabel Queipo-Ortuño, Francisco J Tinahones, Lluís Arola, Antoni Delpino-Rius, Pol Herrero, Núria Canela. Gender-Related Differences on Polyamine Metabolome in Liquid Biopsies by a Simple and Sensitive Two-Step Liquid-Liquid Extraction and LC-MS/MS.
Biomolecules.
2019 11; 9(12):. doi:
10.3390/biom9120779. [PMID: 31779105] - Yohei Shimizu, Amit Rai, Yuko Okawa, Hajime Tomatsu, Masaru Sato, Kota Kera, Hideyuki Suzuki, Kazuki Saito, Mami Yamazaki. Metabolic diversification of nitrogen-containing metabolites by the expression of a heterologous lysine decarboxylase gene in Arabidopsis.
The Plant journal : for cell and molecular biology.
2019 11; 100(3):505-521. doi:
10.1111/tpj.14454. [PMID: 31364191] - Peter Kämpfer, Hans-Jürgen Busse, John A McInroy, Alexis Criscuolo, Dominique Clermont, Stefanie P Glaeser. Xinfangfangia humi sp. nov., isolated from soil amended with humic acid.
International journal of systematic and evolutionary microbiology.
2019 Jul; 69(7):2070-2075. doi:
10.1099/ijsem.0.003434. [PMID: 31099734] - Tünde Kovács, Edit Mikó, András Vida, Éva Sebő, Judit Toth, Tamás Csonka, Anita Boratkó, Gyula Ujlaki, Gréta Lente, Patrik Kovács, Dezső Tóth, Péter Árkosy, Borbála Kiss, Gábor Méhes, James J Goedert, Péter Bai. Cadaverine, a metabolite of the microbiome, reduces breast cancer aggressiveness through trace amino acid receptors.
Scientific reports.
2019 02; 9(1):1300. doi:
10.1038/s41598-018-37664-7. [PMID: 30718646] - Christin Naumann, Jens Müller, Siriwat Sakhonwasee, Annika Wieghaus, Gerd Hause, Marcus Heisters, Katharina Bürstenbinder, Steffen Abel. The Local Phosphate Deficiency Response Activates Endoplasmic Reticulum Stress-Dependent Autophagy.
Plant physiology.
2019 02; 179(2):460-476. doi:
10.1104/pp.18.01379. [PMID: 30510038] - Dujun Wang, Li Zhao, Jiayi Jiang, Jia Liu, Dan Wang, Xiaofeng Yu, Yuan Wei, Zhen Ouyang. Cloning, expression, and functional analysis of lysine decarboxylase in mulberry (Morus alba L.).
Protein expression and purification.
2018 11; 151(?):30-37. doi:
10.1016/j.pep.2018.06.004. [PMID: 29894803] - Dong-Zhi Chen, Ning-Ning Yu, Qi-Ying Chu, Jing Chen, Jie-Xu Ye, Zhuo-Wei Cheng, Shi-Han Zhang, Jian-Meng Chen. Piscinibacter caeni sp. nov., isolated from activated sludge.
International journal of systematic and evolutionary microbiology.
2018 Aug; 68(8):2627-2632. doi:
10.1099/ijsem.0.002891. [PMID: 29957173] - Naji Al-Dubaili, Khaled El-Tarabily, Na'il Saleh. Host-guest complexes of imazalil with cucurbit[8]uril and β-cyclodextrin and their effect on plant pathogenic fungi.
Scientific reports.
2018 02; 8(1):2839. doi:
10.1038/s41598-018-21156-9. [PMID: 29434320] - Nicole M Gibbs, Laura Vaughn Rouhana, Patrick H Masson. Quantitative Trait Loci for Root Growth Response to Cadaverine in Arabidopsis.
Methods in molecular biology (Clifton, N.J.).
2018; 1694(?):233-256. doi:
10.1007/978-1-4939-7398-9_22. [PMID: 29080172] - Baofu Xu, Lei Lei, Xiaocen Zhu, Yiqing Zhou, Youli Xiao. Identification and characterization of L-lysine decarboxylase from Huperzia serrata and its role in the metabolic pathway of lycopodium alkaloid.
Phytochemistry.
2017 Apr; 136(?):23-30. doi:
10.1016/j.phytochem.2016.12.022. [PMID: 28089246] - Martin Levine, Zsolt Lohinai, Ricardo P Teles. Low Biofilm Lysine Content in Refractory Chronic Periodontitis.
Journal of periodontology.
2017 02; 88(2):181-189. doi:
10.1902/jop.2016.160302. [PMID: 27620654] - Weichao Ren, Zhihui Zhang, Wenyong Shao, Yalan Yang, Mingguo Zhou, Changjun Chen. The autophagy-related gene BcATG1 is involved in fungal development and pathogenesis in Botrytis cinerea.
Molecular plant pathology.
2017 02; 18(2):238-248. doi:
10.1111/mpp.12396. [PMID: 26972592] - Liang Chen, Faqiang Li, Shi Xiao. Analysis of Plant Autophagy.
Methods in molecular biology (Clifton, N.J.).
2017; 1662(?):267-280. doi:
10.1007/978-1-4939-7262-3_24. [PMID: 28861836] - Robin Mesnage, Sarah Z Agapito-Tenfen, Vinicius Vilperte, George Renney, Malcolm Ward, Gilles-Eric Séralini, Rubens O Nodari, Michael N Antoniou. An integrated multi-omics analysis of the NK603 Roundup-tolerant GM maize reveals metabolism disturbances caused by the transformation process.
Scientific reports.
2016 12; 6(?):37855. doi:
10.1038/srep37855. [PMID: 27991589] - Petr Soudek, Marina Ursu, Šárka Petrová, Tomáš Vaněk. Improving crop tolerance to heavy metal stress by polyamine application.
Food chemistry.
2016 Dec; 213(?):223-229. doi:
10.1016/j.foodchem.2016.06.087. [PMID: 27451175] - S Eligini, S Fiorelli, E Tremoli, S Colli. Inhibition of transglutaminase 2 reduces efferocytosis in human macrophages: Role of CD14 and SR-AI receptors.
Nutrition, metabolism, and cardiovascular diseases : NMCD.
2016 10; 26(10):922-30. doi:
10.1016/j.numecd.2016.05.011. [PMID: 27378395] - Martin Stenson, Anders Pedersen, Sverker Hasselblom, Herman Nilsson-Ehle, Bengt Göran Karlsson, Rui Pinto, Per-Ola Andersson. Serum nuclear magnetic resonance-based metabolomics and outcome in diffuse large B-cell lymphoma patients - a pilot study.
Leukemia & lymphoma.
2016 08; 57(8):1814-22. doi:
10.3109/10428194.2016.1140164. [PMID: 26887805] - G H M Sagor, Thomas Berberich, Seiji Kojima, Masaru Niitsu, Tomonobu Kusano. Spermine modulates the expression of two probable polyamine transporter genes and determines growth responses to cadaverine in Arabidopsis.
Plant cell reports.
2016 Jun; 35(6):1247-57. doi:
10.1007/s00299-016-1957-3. [PMID: 26905725] - K Kivirand, H Sõmerik, M-L Oldekop, R Rebane, T Rinken. Effect of spermidine and its metabolites on the activity of pea seedlings diamine oxidase and the problems of biosensing of biogenic amines with this enzyme.
Enzyme and microbial technology.
2016 Jan; 82(?):133-137. doi:
10.1016/j.enzmictec.2015.09.007. [PMID: 26672459] - Maria Rosecler Miranda Rossetto, Fabio Vianello, Margarida Juri Saeki, Giuseppina Pace Pereira Lima. Polyamines in conventional and organic vegetables exposed to exogenous ethylene.
Food chemistry.
2015 Dec; 188(?):218-24. doi:
10.1016/j.foodchem.2015.04.125. [PMID: 26041185] - Allison K Strohm, Laura M Vaughn, Patrick H Masson. Natural variation in the expression of ORGANIC CATION TRANSPORTER 1 affects root length responses to cadaverine in Arabidopsis.
Journal of experimental botany.
2015 Feb; 66(3):853-62. doi:
10.1093/jxb/eru444. [PMID: 25403917] - Tomasz Hura, Michał Dziurka, Katarzyna Hura, Agnieszka Ostrowska, Kinga Dziurka. Free and Cell Wall-Bound Polyamines under Long-Term Water Stress Applied at Different Growth Stages of ×Triticosecale Wittm.
PloS one.
2015; 10(8):e0135002. doi:
10.1371/journal.pone.0135002. [PMID: 26247474] - Miguel López-Gómez, Libertad Cobos-Porras, Javier Hidalgo-Castellanos, Carmen Lluch. Occurrence of polyamines in root nodules of Phaseolus vulgaris in symbiosis with Rhizobium tropici in response to salt stress.
Phytochemistry.
2014 Nov; 107(?):32-41. doi:
10.1016/j.phytochem.2014.08.017. [PMID: 25220497] - Ekaterina A Merkulova, Anne Guiboileau, Loreto Naya, Céline Masclaux-Daubresse, Kohki Yoshimoto. Assessment and optimization of autophagy monitoring methods in Arabidopsis roots indicate direct fusion of autophagosomes with vacuoles.
Plant & cell physiology.
2014 Apr; 55(4):715-26. doi:
10.1093/pcp/pcu041. [PMID: 24566535] - Livia Simon-Sarkadi, Ndiko Ludidi, Gábor Kocsy. Modification of cadaverine content by NO in salt-stressed maize.
Plant signaling & behavior.
2014; 9(1):e27598. doi:
10.4161/psb.27598. [PMID: 24398894] - Asif Hameed, Mariyam Shahina, Shih-Yao Lin, Wei-An Lai, Yi-Han Hsu, You-Cheng Liu, Yu-Ming Huang, Chiu-Chung Young. Shimia biformata sp. nov., isolated from surface seawater, and emended description of the genus Shimia Choi and Cho 2006.
International journal of systematic and evolutionary microbiology.
2013 Dec; 63(Pt 12):4533-4539. doi:
10.1099/ijs.0.053553-0. [PMID: 23907225] - Kangseung Lee, Se-Hui Jung, Deok-Hoon Kong, Byeong-Moon Hwang, Eun-Taek Han, Seoung-Woo Park, Jae Hyo Park, Young-Myeong Kim, Kwon-Soo Ha. Comparative characterization of direct and indirect substrate probes for on-chip transamidating activity assay of transglutaminases.
Journal of biotechnology.
2013 Dec; 168(4):324-30. doi:
10.1016/j.jbiotec.2013.10.007. [PMID: 24140601] - Si-rong Liu, Xin-zhou Rong, Gui-cheng Fan, Qing-hui Li, Ya-ming Wei. [Determination and correlation analysis of contents of putrescine, cadaverine, and histamine in necrotic tissue, blood, and urine of patients with diabetic foot].
Zhonghua shao shang za zhi = Zhonghua shaoshang zazhi = Chinese journal of burns.
2013 Dec; 29(6):526-30. doi:
NULL. [PMID: 24495639] - Pushpa C Tomar, Nita Lakra, S N Mishra. Cadaverine: a lysine catabolite involved in plant growth and development.
Plant signaling & behavior.
2013 Oct; 8(10):doi: 10.4161/psb.25850. doi:
10.4161/psb.25850. [PMID: 23887488] - Pushpa C Tomar, Nita Lakra, Shyam Narayan Mishra. Effect of cadaverine on Brassica juncea (L.) under multiple stress.
Indian journal of experimental biology.
2013 Sep; 51(9):758-63. doi:
. [PMID: 24377136] - Jie Cheng, Chi Chen, Krausz W Kristopher, Soumen K Manna, Mike Scerba, Fred K Friedman, Hans Luecke, Jeffrey R Idle, Frank J Gonzalez. Identification of 2-piperidone as a biomarker of CYP2E1 activity through metabolomic phenotyping.
Toxicological sciences : an official journal of the Society of Toxicology.
2013 Sep; 135(1):37-47. doi:
10.1093/toxsci/kft143. [PMID: 23811823] - Rajtilak Majumdar, Lin Shao, Rakesh Minocha, Stephanie Long, Subhash C Minocha. Ornithine: the overlooked molecule in the regulation of polyamine metabolism.
Plant & cell physiology.
2013 Jun; 54(6):990-1004. doi:
10.1093/pcp/pct053. [PMID: 23574701] - Chingju Lin, Shih-Chang Tsai, Michael T Tseng, Shu-Fen Peng, Sheng-Chu Kuo, Meng-Wei Lin, Yuan-Man Hsu, Miau-Rong Lee, Sakae Amagaya, Wen-Wen Huang, Tian-Shung Wu, Jai-Sing Yang. AKT serine/threonine protein kinase modulates baicalin-triggered autophagy in human bladder cancer T24 cells.
International journal of oncology.
2013 Mar; 42(3):993-1000. doi:
10.3892/ijo.2013.1791. [PMID: 23354080] - Kenichi Shibuya, Tomoko Niki, Kazuo Ichimura. Pollination induces autophagy in petunia petals via ethylene.
Journal of experimental botany.
2013 Feb; 64(4):1111-20. doi:
10.1093/jxb/ers395. [PMID: 23349142] - Gui-cheng Fan, Xin-zhou Rong, Xue-min Wang, Si-rong Liu, Yue-ping Zhou, Qing-hui Li. [Influence of exogenous putrescine and cadaverine on pro-inflammatory factors in the peripheral blood of rabbits].
Zhonghua shao shang za zhi = Zhonghua shaoshang zazhi = Chinese journal of burns.
2012 Dec; 28(6):451-4. doi:
. [PMID: 23327914] - Jennifer L Peters, Paul L DeMars, Lindsay M Collins, Julie A Stoner, Hiroyuki Matsumoto, Naoka Komori, Anil Singh, Christa L Feasley, James A Haddock, Martin Levine. Effects of immunization with natural and recombinant lysine decarboxylase on canine gingivitis development.
Vaccine.
2012 Oct; 30(47):6706-12. doi:
10.1016/j.vaccine.2012.08.028. [PMID: 22975025] - Ran Liu, Kaishun Bi, Ying Jia, Qian Wang, Ran Yin, Qing Li. Determination of polyamines in human plasma by high-performance liquid chromatography coupled with Q-TOF mass spectrometry.
Journal of mass spectrometry : JMS.
2012 Oct; 47(10):1341-6. doi:
10.1002/jms.3084. [PMID: 23019166] - E Songisepp, P Hütt, M Rätsep, E Shkut, S Kõljalg, K Truusalu, J Stsepetova, I Smidt, H Kolk, M Zagura, M Mikelsaar. Safety of a probiotic cheese containing Lactobacillus plantarum Tensia according to a variety of health indices in different age groups.
Journal of dairy science.
2012 Oct; 95(10):5495-509. doi:
10.3168/jds.2011-4756. [PMID: 22863096] - Jieyin Sun, Hiroyuki Morita, Guoshen Chen, Hiroshi Noguchi, Ikuro Abe. Molecular cloning and characterization of copper amine oxidase from Huperzia serrata.
Bioorganic & medicinal chemistry letters.
2012 Sep; 22(18):5784-90. doi:
10.1016/j.bmcl.2012.07.102. [PMID: 22901898] - Zsolt Lohinai, Beata Keremi, Eva Szoko, Tamas Tabi, Csaba Szabo, Zsolt Tulassay, Martin Levine. Bacterial lysine decarboxylase influences human dental biofilm lysine content, biofilm accumulation, and subclinical gingival inflammation.
Journal of periodontology.
2012 Aug; 83(8):1048-56. doi:
10.1902/jop.2011.110474. [PMID: 22141361] - Arthur S Brecher, Anum H Riaz. Polyamines detoxify the anticoagulant effect of acetaldehyde on prothrombin time.
Journal of cardiovascular pharmacology.
2012 Jul; 60(1):1-7. doi:
10.1097/fjc.0b013e318251f98d. [PMID: 22407337] - Jose A Gil-Amado, Maria C Gomez-Jimenez. Regulation of polyamine metabolism and biosynthetic gene expression during olive mature-fruit abscission.
Planta.
2012 Jun; 235(6):1221-37. doi:
10.1007/s00425-011-1570-1. [PMID: 22167259] - Mohamed A Farag, Andrea Porzel, Ludger A Wessjohann. Comparative metabolite profiling and fingerprinting of medicinal licorice roots using a multiplex approach of GC-MS, LC-MS and 1D NMR techniques.
Phytochemistry.
2012 Apr; 76(?):60-72. doi:
10.1016/j.phytochem.2011.12.010. [PMID: 22336263] - Somnuk Bunsupa, Kae Katayama, Emi Ikeura, Akira Oikawa, Kiminori Toyooka, Kazuki Saito, Mami Yamazaki. Lysine decarboxylase catalyzes the first step of quinolizidine alkaloid biosynthesis and coevolved with alkaloid production in leguminosae.
The Plant cell.
2012 Mar; 24(3):1202-16. doi:
10.1105/tpc.112.095885. [PMID: 22415272] - Young-Man Kim, Sung-Eun Lee, Byeoung-Soo Park, Mi-Kyung Son, Young-Mi Jung, Seung-Ok Yang, Hyung-Kyoon Choi, Sung-Ho Hur, Jong Hwa Yum. Proteomic analysis on acetate metabolism in Citrobacter sp. BL-4.
International journal of biological sciences.
2012; 8(1):66-78. doi:
10.7150/ijbs.8.66. [PMID: 22211106] - P Paulsen, S Vali, F Bauer. Quality traits of wild boar mould-ripened salami manufactured with different selections of meat and fat tissue, and with and without bacterial starter cultures.
Meat science.
2011 Dec; 89(4):486-90. doi:
10.1016/j.meatsci.2011.05.014. [PMID: 21664055] - Gwénaëlle Le Gall, Samah O Noor, Karyn Ridgway, Louise Scovell, Crawford Jamieson, Ian T Johnson, Ian J Colquhoun, E Kate Kemsley, Arjan Narbad. Metabolomics of fecal extracts detects altered metabolic activity of gut microbiota in ulcerative colitis and irritable bowel syndrome.
Journal of proteome research.
2011 Sep; 10(9):4208-18. doi:
10.1021/pr2003598. [PMID: 21761941] - Akira Ikari, Ayumi Takiguchi, Kosuke Atomi, Junko Sugatani. Epidermal growth factor increases clathrin-dependent endocytosis and degradation of claudin-2 protein in MDCK II cells.
Journal of cellular physiology.
2011 Sep; 226(9):2448-56. doi:
10.1002/jcp.22590. [PMID: 21660968] - María Paula Campestre, Cesar Daniel Bordenave, Andrea Cecilia Origone, Ana Bernardina Menéndez, Oscar Adolfo Ruiz, Andrés Alberto Rodríguez, Santiago Javier Maiale. Polyamine catabolism is involved in response to salt stress in soybean hypocotyls.
Journal of plant physiology.
2011 Jul; 168(11):1234-40. doi:
10.1016/j.jplph.2011.01.007. [PMID: 21324548] - Katie M Lowther, Viacheslav O Nikolaev, Lisa M Mehlmann. Endocytosis in the mouse oocyte and its contribution to cAMP signaling during meiotic arrest.
Reproduction (Cambridge, England).
2011 Jun; 141(6):737-47. doi:
10.1530/rep-10-0461. [PMID: 21411693] - N I Shevyakova, E N Il'ina, L A Stetsenko, Vl V Kuznetsov. Nickel accumulation in rape shoots (Brassica napus L.) increased by putrescine.
International journal of phytoremediation.
2011 Apr; 13(4):345-56. doi:
10.1080/15226514.2010.495147. [PMID: 21598797] - Ai-Dong Qi, Dayle Houston-Cohen, Isabella Naruszewicz, T Kendall Harden, Robert A Nicholas. Ser352 and Ser354 in the carboxyl terminus of the human P2Y(1) receptor are required for agonist-promoted phosphorylation and internalization in MDCK cells.
British journal of pharmacology.
2011 Mar; 162(6):1304-13. doi:
10.1111/j.1476-5381.2010.01135.x. [PMID: 21108629] - Chien-Hsun Huang, Fwu-Ling Lee, Chih-Jen Tien, Pei-Wen Hsieh. Rhodotorula taiwanensis sp. nov., a novel yeast species from a plant in Taiwan.
Antonie van Leeuwenhoek.
2011 Feb; 99(2):297-302. doi:
10.1007/s10482-010-9489-2. [PMID: 20680683] - Raúl A Almeida, Belgin Dogan, Suzanne Klaessing, Ynte H Schukken, Stephen P Oliver. Intracellular fate of strains of Escherichia coli isolated from dairy cows with acute or chronic mastitis.
Veterinary research communications.
2011 Feb; 35(2):89-101. doi:
10.1007/s11259-010-9455-5. [PMID: 21207146] - Melissa S Hillwig, Anthony L Contento, Alexander Meyer, Danielle Ebany, Diane C Bassham, Gustavo C Macintosh. RNS2, a conserved member of the RNase T2 family, is necessary for ribosomal RNA decay in plants.
Proceedings of the National Academy of Sciences of the United States of America.
2011 Jan; 108(3):1093-8. doi:
10.1073/pnas.1009809108. [PMID: 21199950] - Ran Liu, Ying Jia, Weiming Cheng, Junhong Ling, Lili Liu, Kaishun Bi, Qing Li. Determination of polyamines in human urine by precolumn derivatization with benzoyl chloride and high-performance liquid chromatography coupled with Q-time-of-flight mass spectrometry.
Talanta.
2011 Jan; 83(3):751-6. doi:
10.1016/j.talanta.2010.10.039. [PMID: 21147316] - Kévin Baranger, Marie-Louise Zani, Valérie Labas, Sandrine Dallet-Choisy, Thierry Moreau. Secretory leukocyte protease inhibitor (SLPI) is, like its homologue trappin-2 (pre-elafin), a transglutaminase substrate.
PloS one.
2011; 6(6):e20976. doi:
10.1371/journal.pone.0020976. [PMID: 21687692] - Donald M Gardiner, Kemal Kazan, Sebastien Praud, Francois J Torney, Anca Rusu, John M Manners. Early activation of wheat polyamine biosynthesis during Fusarium head blight implicates putrescine as an inducer of trichothecene mycotoxin production.
BMC plant biology.
2010 Dec; 10(?):289. doi:
10.1186/1471-2229-10-289. [PMID: 21192794] - Maria C Gomez-Jimenez, Miguel A Paredes, Mercedes Gallardo, Isabel M Sanchez-Calle. Mature fruit abscission is associated with up-regulation of polyamine metabolism in the olive abscission zone.
Journal of plant physiology.
2010 Nov; 167(17):1432-41. doi:
10.1016/j.jplph.2010.05.020. [PMID: 20643493] - Sikander Pal Choudhary, Renu Bhardwaj, Bishan Datt Gupta, Prabhu Dutt, Rajinder Kumar Gupta, Stefania Biondi, Mukesh Kanwar. Epibrassinolide induces changes in indole-3-acetic acid, abscisic acid and polyamine concentrations and enhances antioxidant potential of radish seedlings under copper stress.
Physiologia plantarum.
2010 Nov; 140(3):280-96. doi:
10.1111/j.1399-3054.2010.01403.x. [PMID: 20681975] - Hongmei Luo, Ying Li, Chao Sun, Qiong Wu, Jingyuan Song, Yongzhen Sun, André Steinmetz, Shilin Chen. Comparison of 454-ESTs from Huperzia serrata and Phlegmariurus carinatus reveals putative genes involved in lycopodium alkaloid biosynthesis and developmental regulation.
BMC plant biology.
2010 Sep; 10(?):209. doi:
10.1186/1471-2229-10-209. [PMID: 20854695] - K A Barry, B J Wojcicki, I S Middelbos, B M Vester, K S Swanson, G C Fahey. Dietary cellulose, fructooligosaccharides, and pectin modify fecal protein catabolites and microbial populations in adult cats.
Journal of animal science.
2010 Sep; 88(9):2978-87. doi:
10.2527/jas.2009-2464. [PMID: 20495116] - Fan Cheng, Patricia J McLaughlin, William A Banks, Ian S Zagon. Internalization of the opioid growth factor, [Met5]-enkephalin, is dependent on clathrin-mediated endocytosis for downregulation of cell proliferation.
American journal of physiology. Regulatory, integrative and comparative physiology.
2010 Sep; 299(3):R774-85. doi:
10.1152/ajpregu.00318.2010. [PMID: 20592180] - P Kämpfer, E Falsen, S Langer, N Lodders, H-J Busse. Paenalcaligenes hominis gen. nov., sp. nov., a new member of the family Alcaligenaceae.
International journal of systematic and evolutionary microbiology.
2010 Jul; 60(Pt 7):1537-1542. doi:
10.1099/ijs.0.016576-0. [PMID: 19684310] - Maira Goytia, William M Shafer. Polyamines can increase resistance of Neisseria gonorrhoeae to mediators of the innate human host defense.
Infection and immunity.
2010 Jul; 78(7):3187-95. doi:
10.1128/iai.01301-09. [PMID: 20439477] - Masato Ohe, Hitomi Sasaki, Masaru Niitsu, Nello Bagni, Annalisa Tassoni, Shigeru Matsuzaki. Cadaverine turnover in soybean seedlings using 15N-labelled lysine and cadaverine.
Plant physiology and biochemistry : PPB.
2010 Jul; 48(7):591-5. doi:
10.1016/j.plaphy.2010.01.018. [PMID: 20153659] - Shih T Khew, Pradeep P Panengad, Michael Raghunath, Yen W Tong. Characterization of amine donor and acceptor sites for tissue type transglutaminase using a sequence from the C-terminus of human fibrillin-1 and the N-terminus of osteonectin.
Biomaterials.
2010 Jun; 31(16):4600-8. doi:
10.1016/j.biomaterials.2010.01.094. [PMID: 20223517] - Safiyh Taghavi, Daniel van der Lelie, Adam Hoffman, Yian-Biao Zhang, Michael D Walla, Jaco Vangronsveld, Lee Newman, Sébastien Monchy. Genome sequence of the plant growth promoting endophytic bacterium Enterobacter sp. 638.
PLoS genetics.
2010 May; 6(5):e1000943. doi:
10.1371/journal.pgen.1000943. [PMID: 20485560] - Peter Kämpfer, Jenny Schäfer, Nicole Lodders, Hans-Jürgen Busse. Brevibacterium sandarakinum sp. nov., isolated from a wall of an indoor environment.
International journal of systematic and evolutionary microbiology.
2010 Apr; 60(Pt 4):909-913. doi:
10.1099/ijs.0.014100-0. [PMID: 19661519] - Astrid Heide Sziderics, Mouhssin Oufir, Friederike Trognitz, Dieter Kopecky, Ildikó Matusíková, Jean-Francois Hausman, Eva Wilhelm. Organ-specific defence strategies of pepper (Capsicum annuum L.) during early phase of water deficit.
Plant cell reports.
2010 Mar; 29(3):295-305. doi:
10.1007/s00299-010-0822-z. [PMID: 20087595] - Rachel S Poretsky, Shulei Sun, Xiaozhen Mou, Mary Ann Moran. Transporter genes expressed by coastal bacterioplankton in response to dissolved organic carbon.
Environmental microbiology.
2010 Mar; 12(3):616-27. doi:
10.1111/j.1462-2920.2009.02102.x. [PMID: 19930445] - Rika Ozawa, Cinzia M Bertea, Maria Foti, Ravishankar Narayana, Gen-Ichiro Arimura, Atsushi Muroi, Massimo E Maffei, Junji Takabayashi. Polyamines and jasmonic acid induce plasma membrane potential variations in Lima bean.
Plant signaling & behavior.
2010 Mar; 5(3):308-10. doi:
10.4161/psb.5.3.10848. [PMID: 20200489] - Yaodong Zhao, Qiang Huang, Jicheng Yang, Meiqing Lou, Aidong Wang, Jun Dong, Zhenghong Qin, Tianyi Zhang. Autophagy impairment inhibits differentiation of glioma stem/progenitor cells.
Brain research.
2010 Feb; 1313(?):250-8. doi:
10.1016/j.brainres.2009.12.004. [PMID: 20004652] - Zita Kovács, Livia Simon-Sarkadi, Attila Szucs, Gábor Kocsy. Differential effects of cold, osmotic stress and abscisic acid on polyamine accumulation in wheat.
Amino acids.
2010 Feb; 38(2):623-31. doi:
10.1007/s00726-009-0423-8. [PMID: 19960214] - Rika Ozawa, Cinzia M Bertea, Maria Foti, Ravishankar Narayana, Gen-Ichiro Arimura, Atsushi Muroi, Jun-Ichiro Horiuchi, Takaaki Nishioka, Massimo E Maffei, Junji Takabayashi. Exogenous polyamines elicit herbivore-induced volatiles in lima bean leaves: involvement of calcium, H2O2 and Jasmonic acid.
Plant & cell physiology.
2009 Dec; 50(12):2183-99. doi:
10.1093/pcp/pcp153. [PMID: 19884250] - Jin-Young Park, Se-Hui Jung, Jae-Wan Jung, Mi-Hye Kwon, Je-Ok Yoo, Young-Myeong Kim, Kwon-Soo Ha. A novel array-based assay of in situ tissue transglutaminase activity in human umbilical vein endothelial cells.
Analytical biochemistry.
2009 Nov; 394(2):217-22. doi:
10.1016/j.ab.2009.07.040. [PMID: 19646948] - Gabriella Szalai, Mátyás Pap, Tibor Janda. Light-induced frost tolerance differs in winter and spring wheat plants.
Journal of plant physiology.
2009 Nov; 166(16):1826-31. doi:
10.1016/j.jplph.2009.04.016. [PMID: 19481291] - Peter Kämpfer, Hans-Jürgen Busse, Holger C Scholz. Chromobacterium piscinae sp. nov. and Chromobacterium pseudoviolaceum sp. nov., from environmental samples.
International journal of systematic and evolutionary microbiology.
2009 Oct; 59(Pt 10):2486-90. doi:
10.1099/ijs.0.008888-0. [PMID: 19622653] - Asier Jayo, Isabel Conde, Pedro Lastres, Victor Jiménez-Yuste, Consuelo González-Manchón. Possible role for cellular FXIII in monocyte-derived dendritic cell motility.
European journal of cell biology.
2009 Aug; 88(8):423-31. doi:
10.1016/j.ejcb.2009.04.002. [PMID: 19477035] - Hajo Zech, Sebastian Thole, Kerstin Schreiber, Daniela Kalhöfer, Sonja Voget, Thorsten Brinkhoff, Meinhard Simon, Dietmar Schomburg, Ralf Rabus. Growth phase-dependent global protein and metabolite profiles of Phaeobacter gallaeciensis strain DSM 17395, a member of the marine Roseobacter-clade.
Proteomics.
2009 Jul; 9(14):3677-97. doi:
10.1002/pmic.200900120. [PMID: 19639587]