Related Experiment Video
Updated: Apr 1, 2026

08:55
Facile Protocol for the Synthesis of Self-assembling Polyamine-based Peptide Amphiphiles PPAs and Related Biomaterials
Published on: June 25, 2018
8.6K
Biosynthesis of Arginine and Polyamines
Ecosal Plus
|October 8, 2015
Summary
This review details arginine biosynthesis regulation in E. coli and Salmonella, focusing on the arginine repressor, gene evolution, and carbamoylphosphate
Area of Science:
- Microbiology and Molecular Biology
- Metabolic Regulation and Biosynthesis Pathways
Background:
- Arginine biosynthesis regulation is fundamental to understanding metabolic control.
- Significant progress in the last decade includes understanding the arginine repressor's structure and function in E. coli and Salmonella.
- Sequence analysis of arg structural genes in E. coli and Salmonella has provided evolutionary insights.
Purpose of the Study:
- To provide a comprehensive overview of arginine and polyamine biosynthesis pathways.
- To elucidate the regulatory circuits governing these pathways and their interconnections.
- To highlight the dual regulation of the carAB operon and the role of carbamoylphosphate.
Main Methods:
- Review of early investigations and recent advances in arginine biosynthesis.
- Comparative sequence analysis of arg structural genes in E. coli and Salmonella.
- Examination of regulatory mechanisms, including the arginine repressor and operon regulation.
Main Results:
- Identified homologous genes for arginine biosynthesis enzymes in E. coli and S. enterica serovar Typhimurium, with the exception of argF in Salmonella.
- Carbamoylphosphate synthetase (CPSase) produces carbamoylphosphate, a common precursor for arginine and pyrimidines, using glutamine as the amino group donor in E. coli and Salmonella.
- Highlighted differences in CPSase and arginine/pyrimidine biosynthesis enzyme specificity compared to Bacillus subtilis and fungi.
Conclusions:
- The arginine repressor plays a key role in metabolic regulation in E. coli and Salmonella.
- Comparative genomics reveals evolutionary relationships and differences in arginine biosynthesis pathways.
- Interconnections between arginine, pyrimidine, and polyamine biosynthesis are significant, with carbamoylphosphate as a central precursor.
Related Concept Videos
Amino Acid Biosynthetic Pathways
1.6K
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...
1.6K
Biosynthesis of Nucleic Acids
1.5K
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...
1.5K
Preparation of Amines: Alkylation of Ammonia and Amines
5.1K
Alkylation is one of the methods used to prepare amines. Direct alkylation of ammonia or a primary amine with an alkyl halide gives polyalkylated amines along with a quaternary ammonium salt through successive SN2 reactions. This process of making the quaternary salt through the direct alkylation method is called exhaustive alkylation.
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
Each alkylation step makes the nitrogen center more nucleophilic, which triggers successive alkylations until a quaternary ammonium salt is formed. Considering...
5.1K
Preparation of 1° Amines: Azide Synthesis
4.8K
Direct alkylation of ammonia produces polyalkylated amines, along with a quaternary ammonium salt. To exclusively prepare primary amines, the azide synthesis method can be used.
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
4.8K
Amines: Introduction
6.3K
Amines are organic derivatives of ammonia. They are formed by replacing one or more ammonia protons with alkyl or aryl groups. Depending upon the number of organyl groups bonded to nitrogen, amines are classified as primary, secondary, or tertiary. Primary amines have one organyl group attached to the nitrogen atom, while secondary and tertiary amines have two and three organyl groups attached to the nitrogen atom, respectively.
6.3K
Urea Cycle
52.1K
The urea cycle describes how liver cells convert ammonia to urea. Ammonia is a toxic waste product of protein catabolism. Land animals must convert ammonia into the less toxic urea which can be safely eliminated by the kidneys through urine. Marine animals excrete ammonia directly, and the surrounding water dilutes the ammonia to safe levels.
52.1K

