Target type: biologicalprocess
The chemical reactions and pathways resulting in the formation of homoserine, alpha-amino-gamma-hydroxybutyric acid. [GOC:go_curators, ISBN:0198506732]
Homoserine biosynthesis is a metabolic pathway essential for the production of the amino acid homoserine, a key precursor for several important metabolites, including threonine, methionine, and isoleucine. This process primarily occurs in bacteria, fungi, and plants, and is absent in mammals.
The starting point for homoserine biosynthesis is the amino acid aspartic acid. The pathway can be divided into two main stages:
**Stage 1: Aspartate to Aspartyl-semialdehyde**
1. **Aspartate kinase (AK) catalyzes the phosphorylation of aspartate to β-aspartyl phosphate using ATP as the phosphate donor.** This step is regulated by feedback inhibition by threonine, methionine, and isoleucine, ensuring balanced production of these amino acids.
2. **Aspartate-semialdehyde dehydrogenase (ASDH) converts β-aspartyl phosphate to aspartyl-semialdehyde.** This is a critical step as it involves the reduction of a carboxyl group to an aldehyde group, requiring NAD(P)H as a cofactor.
**Stage 2: Aspartyl-semialdehyde to Homoserine**
1. **Homoserine dehydrogenase (HSD) catalyzes the NAD(P)H-dependent reduction of aspartyl-semialdehyde to homoserine.** This is the final step in the pathway and is also regulated by feedback inhibition by threonine.
**Overall, the homoserine biosynthetic pathway can be summarized as follows:**
Aspartate → β-aspartyl phosphate → Aspartyl-semialdehyde → Homoserine
**The biological significance of homoserine biosynthesis lies in its central role in providing essential amino acids for diverse cellular functions:**
* **Threonine:** A vital component of proteins and involved in various metabolic pathways.
* **Methionine:** A key amino acid in protein synthesis and a precursor for several important molecules like S-adenosyl methionine (SAM), involved in methylation reactions.
* **Isoleucine:** A crucial amino acid for protein synthesis and involved in energy metabolism.
**Variations and Regulatory Mechanisms**
The specific enzymes involved in homoserine biosynthesis and their regulatory mechanisms can vary depending on the organism. Some bacteria, for instance, utilize a single bifunctional enzyme combining AK and ASDH activities. Additionally, the pathway is tightly regulated to ensure efficient production of homoserine and its derivatives while maintaining cellular homeostasis.
The homoserine biosynthetic pathway is an intricate and essential metabolic process that plays a critical role in providing vital amino acids for diverse biological functions. Its regulation and variations across different organisms highlight the intricate interconnectedness of metabolism and its adaptation to diverse environmental conditions.'"
Protein | Definition | Taxonomy |
---|---|---|
Bifunctional aspartokinase/homoserine dehydrogenase 1 | A bifunctional aspartokinase/homoserine dehydrogenase 1 that is encoded in the genome of Escherichia coli K-12. [PRO:DNx, UniProtKB:P00561] | Escherichia coli K-12 |
Bifunctional aspartokinase/homoserine dehydrogenase 1 | A bifunctional aspartokinase/homoserine dehydrogenase 1 that is encoded in the genome of Escherichia coli K-12. [PRO:DNx, UniProtKB:P00561] | Escherichia coli K-12 |
Compound | Definition | Classes | Roles |
---|---|---|---|
glutamic acid | glutamic acid : An alpha-amino acid that is glutaric acid bearing a single amino substituent at position 2. Glutamic Acid: A non-essential amino acid naturally occurring in the L-form. Glutamic acid is the most common excitatory neurotransmitter in the CENTRAL NERVOUS SYSTEM. | glutamic acid; glutamine family amino acid; L-alpha-amino acid; proteinogenic amino acid | Escherichia coli metabolite; ferroptosis inducer; micronutrient; mouse metabolite; neurotransmitter; nutraceutical |
beta-aminoglutaric acid | 3-aminoglutaric acid: RN given refers to parent cpd; structure given in first source isoglutamic acid : A 1,5-dicarboxylic acid compound having a 3-amino substituent. It has been isolated from the extracts of the algae, Chondria armata. | dicarboxylic acid | algal metabolite; marine metabolite |