尼古丁胺胺单核酸的绿色制造合成:途径,催化剂和前景
Feng Peng1, Wei Ke1, Xiao-Yuan Jin1
1College of Biology and Environmental Engineering, Zhejiang Shuren University, Hangzhou 310015, PR China.
Bioorganic chemistry
|March 4, 2026
概括
功能性辅酶对生物过程至关重要,面临着日益增长的市场需求. 本综述强调了生物制造战略,重点是尼古丁胺单核酸 (NMN) 合成,以提高生产效率和行业竞争力.
科学领域:
- 生物化学 生物化学
- 生物技术是生物技术.
- 代谢工程是代谢工程.
背景情况:
- 功能性辅酶是重要的有机小分子,对酶催化反应和细胞代谢至关重要.
- 由于全球人口老龄化和健康意识的提高,市场对辅酶的需求正在迅速增加.
- 生物制造为辅酶行业提供了提高生产效率,降低成本和创新.
研究的目的:
- 系统地审查当前的辅酶合成技术,重点关注β-尼古丁胺胺 mononucleotide (NMN).
- 强调NMN的发酵和酶合成中的多策略方法.
- 建议跨学科的研究方向,以持续创新共酶生物制造.
主要方法:
- 在NMN合成中对酶分类,辅因子再生和竞争性途径调节的审查.
- 对运输系统优化策略进行分析,以提高NMN生产.
- 探索系统代谢工程和合发酵过程优化.
主要成果:
- 详细检查了NMN发酵和酶合成中应用的各种策略.
- 识别关键酶用于选,工程和NMN生物制造中的应用.
- 强调跨学科方法对流程优化的重要性.
结论:
- 生物制造,特别是通过先进的合成策略,是满足对NMN等功能共酶日益增长的需求的关键.
- 酶技术和系统代谢工程的持续创新将推动辅酶行业的高质量发展.
- 优化生物制造工艺将提高辅酶行业的国际竞争力.
相关概念视频
Biosynthesis of Nucleic Acids
1.4K
Nucleic acid biosynthesis is a fundamental biochemical process that produces the purine and pyrimidine nucleotides essential for DNA and RNA synthesis. This pathway maintains a balanced nucleotide pool, preventing imbalances that could jeopardize genetic integrity and cellular function. Given the crucial role of nucleotides, their synthesis is tightly regulated to ensure proper cellular homeostasis.Purine BiosynthesisThe biosynthesis of purine nucleotides begins with ribose-5-phosphate, a...
1.4K
Role of Reduced Coenzymes NADH and FADH₂
18.1K
The energy released from the breakdown of the chemical bonds within nutrients can be stored either through the reduction of electron carriers or in the bonds of adenosine triphosphate (ATP). In living systems, a small class of compounds functions as mobile electron carriers, molecules that bind to and shuttle high-energy electrons between compounds in pathways. The principal electron carriers that will be considered originate from the B vitamin group and are derivatives of nucleotides; they are...
18.1K
Amino Acid Biosynthetic Pathways
1.5K
Amino acid biosynthesis is essential for cell growth, protein synthesis, and metabolic regulation. Cells generate essential and non-essential amino acids from metabolic intermediates to sustain vital biological functions. These intermediates originate from key metabolic pathways: glycolysis, the tricarboxylic acid (TCA) cycle, and the pentose phosphate pathway. Important precursors include α-ketoglutarate, pyruvate, oxaloacetate, phosphoenolpyruvate, and erythrose-4-phosphate, which...
1.5K
Other Glycolytic Pathways
1.1K
The pentose phosphate pathway (PPP) operates in parallel with glycolysis, facilitating the metabolism of both pentoses and glucose. This pathway consists of two distinct phases: the oxidative and non-oxidative phases. While it does not directly generate ATP, the intermediates formed during the process can integrate into glycolysis, contributing to cellular energy metabolism when required.Oxidative Phase: NADPH ProductionThe oxidative phase of the pentose phosphate pathway is primarily...
1.1K
Inorganic Nitrogen Assimilation
702
Nitrogen is an essential element in biological systems, forming a crucial component of proteins, nucleic acids, and other cellular constituents. Many bacteria and archaea acquire nitrogen in the form of nitrate (NO₃⁻) or ammonia (NH₃), which are then assimilated into biomolecules through specific enzymatic pathways.Assimilatory Nitrate ReductionWhen nitrate enters the cell, it undergoes a two-step reduction process known as assimilatory nitrate reduction. Initially, the enzyme...
702
Preparation of Amines: Reduction of Oximes and Nitro Compounds
4.8K
Oximes can be reduced to primary amines using catalytic hydrogenation, hydride reduction, or sodium metal reduction. The reduction of aliphatic and aromatic nitro compounds to primary amines takes place by either catalytic hydrogenation or by using active metals like Fe, Zn, and Sn in the presence of an acid.
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
4.8K


