关于黑色科霍什 (Actaea racemosa L.) 中生物活性胺的生物合成
Martin J Spiering1, James F Parsons1, Edward Eisenstein1,2
1Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850, USA.
Plants (Basel, Switzerland)
|January 25, 2025
概括
黑色科霍什 (Actaea racemosa) 含有三聚二甲酸脱酶 (TDC) 酶,可以产生胺,这是血清素的前体. 较高的TDC活性对于这种植物的血清素生产至关重要.
科学领域:
- 植物生物化学和分子生物学
- 植物化学 植物化学
- 药理学是指药理学,即药理学是指药理学.
背景情况:
- 植物补充剂,如黑 (Actaea racemosa) 具有复杂的作用机制和安全问题.
- 生物活性模拟物N-甲基色胺存在于A. racemosa中,并有助于其色胺活性.
- 假设三脱氧酶 (TDC) 酶可以将L-三转化为三胺,这是血清素前体.
研究的目的:
- 为了研究黑TDC类基因在胺和胺生物合成中的作用.
- 描述黑TDCs的活性及其对血清激素化合物生产的贡献.
- 在A. racemosa. 中识别和量化血清衍生物.
主要方法:
- 在Saccharomyces cerevisiae中克隆和表达黑TDC基因 (TDC1,TDC2,TDC3).
- 在酵母中与三胺5-基酶 (T5H) 共同表达TDC,以评估血清素的产量.
- 位点定向突变发生,以确定TDC活性位点中的关键残留物.
- 使用LC-MS进行植物化学分析,以检测和量化A. racemosa组织中的胺.
- 用三胺和N-甲基三胺对A. racemosa叶组织进行化.
主要成果:
- 在酵母产生的氨酸中表达黑色TDC1,TDC2和TDC3.
- 与TDC2相比,TDC1和TDC3的活性较高,与可变活性部位残留物有关.
- 高活性TDC与大米T5H的同时表达产生了血清素,表明TDC活性是限制速度的步骤.
- 在LC-MS分析中,在A. racemosa.中发现了三胺,血清素,N-甲基血清素和布福因.
- 化实验表明,甲基化在N-甲基胺生物合成中先于化.
结论:
- 黑TDC酶在胺和随后的胺化合物的生物合成中发挥着关键作用.
- 在A. racemosa.中,TDCs的活性是产生血清素及其衍生物的关键决定因素.
- 黑色中存在比以前知道的更多种类型的血清素衍生物,包括潜在的有毒布福因,比以前知道的更多.
相关概念视频
Cholinergic Antagonists: Chemistry and Structure-Activity Relationship
2.1K
Cholinergic antagonists bind to cholinergic receptors and limit the effects of acetylcholine and other cholinergic agonists. Based on the specific cholinergic receptor affinity, these antagonists are classified as muscarinic or nicotinic. Anticholinergics interrupt parasympathetic innervations while sympathetic innervations remain uninterrupted. Muscarinic antagonists are also called 'muscarinic antagonists', 'antimuscarinics', or 'parasympatholytics'. Nicotinic...
2.1K
Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
515
Indirect-acting cholinergic agonists are agents that interact with the acetylcholinesterase enzyme in the synaptic cleft, preventing the breakdown of acetylcholine into choline and acetate. Consequently, the concentration of acetylcholine in the synaptic cleft increases. These agonists can be classified into reversible and irreversible inhibitors based on their duration of action.
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
515
Drugs Affecting Neurotransmitter Synthesis
1.2K
Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase,...
1.2K


