Oryzalexin S biosynthesis: a cross-stitched disappearing pathway
Le Zhao1, Richard Oyagbenro1, Yiling Feng1
1Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011 USA.
Abiotech
|May 23, 2023
Summary
Rice phytoalexin biosynthesis involves two gene clusters, with oryzalexin S production dependent on genes from both. Subspecies-specific gene presence explains variations in oryzalexin S production between rice varieties.
Area of Science:
- Plant biochemistry and molecular biology
- Genomics and metabolomics of crop plants
- Natural product biosynthesis in cereals
Background:
- Rice produces diterpenoid phytoalexins crucial for its defense mechanisms.
- Biosynthetic gene clusters (BGCs) in rice encode enzymes for these natural products.
- The chromosome 4 BGC (c4BGC) is linked to momilactone production via OsCPS4.
Purpose of the Study:
- To elucidate the complete biosynthetic pathway of the rice phytoalexin oryzalexin S.
- To identify the specific cytochrome P450 (CYP) monooxygenases involved in oryzalexin S production.
- To investigate the genetic basis for subspecies-specific differences in oryzalexin S biosynthesis.
Main Methods:
- Analysis of gene locations within rice BGCs.
- Enzymatic characterization of CYP99A2, CYP99A3, CYP71Z21, and CYP71Z22.
- Comparative genomics of BGCs across rice subspecies (ssp. japonica and ssp. indica).
Main Results:
- Oryzalexin S biosynthesis requires enzymes encoded by two distinct BGCs: c4BGC and the chromosome 7 BGC (c7BGC).
- CYP99A2/A3 catalyze C19-hydroxylation, while CYP71Z21/Z22 catalyze C2α-hydroxylation, both essential steps for oryzalexin S.
- The c7BGC is prevalent in ssp. japonica but rare in ssp. indica, correlating with oryzalexin S production differences.
Conclusions:
- Oryzalexin S biosynthesis is a complex, cross-stitched pathway involving multiple BGCs.
- Subspecies-specific distribution of the c7BGC underlies variations in oryzalexin S production.
- Evidence suggests introgression of ssp. indica alleles (OsKSL11) into japonica, leading to loss of oryzalexin S production in some japonica varieties.
More Related Videos
Related Concept Videos
Amino Acid Biosynthetic Pathways
47
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...
47
Biosynthesis in Bacteria
42
Biosynthesis in bacteria is a fundamental anabolic process that generates essential macromolecules, including proteins, nucleic acids, lipids, and polysaccharides. These macromolecules are critical for cellular growth, replication, and function. The process is tightly regulated and energetically linked to catabolic pathways to ensure optimal resource utilization.Biosynthetic pathways begin with precursor metabolites such as pyruvate, acetyl-CoA, and glucose-6-phosphate derived from glycolysis,...
42
Biosynthesis of Lipids
44
Microbial membranes exhibit remarkable diversity in lipid composition, reflecting evolutionary adaptations to various environmental conditions. The three domains of life—Bacteria, Archaea, and Eukarya—synthesize membrane lipids through distinct biosynthetic pathways, leading to fundamental structural differences that impact membrane stability, function, and adaptability.Fatty Acid-Based Lipids in Bacteria and EukaryaBacteria and eukaryotes share a common fatty acid biosynthesis...
44
Preparation of Epoxides
7.9K
Overview
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of...
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of...
7.9K
Formation of Lipopolysaccharides
56
Lipopolysaccharides (LPS) are crucial components of the outer membrane of Gram-negative bacteria, serving both structural and functional roles. It contributes to membrane stability and protects bacteria from host immune responses. LPS is composed of three major regions—lipid A, a core oligosaccharide, and an O antigen. The biosynthesis and assembly of LPS involve a highly coordinated set of enzymatic reactions and transport mechanisms. Additionally, LPS is recognized as an endotoxin,...
56
Peptidoglycan Synthesis
78
Structure of PeptidoglycanPeptidoglycan is a vital structural component of the bacterial cell wall, providing mechanical strength and shape to the cell. It consists of repeating units of two sugars—N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM)—linked by β-1,4 glycosidic bonds. These sugar chains are cross-linked by short peptide chains, forming a mesh-like polymer that surrounds the bacterial plasma membrane.Cytoplasmic Phase – Precursor SynthesisPeptidoglycan...
78


