Metabolic pathways
Last update on the 30th of April, 2018A metabolic pathway of carotenoid biosynthesis is studied in KEGG database.
Basic information about the pathway
The carotenoid biosynthesis pathway is stored in KEGG DB under map00906 accession and shown in figure 1. Carotenoids are plant isoprenoid pigments possessing extended conjugated polyene bonds. Main functions are photoprotection and light collection in chloroplasts. The initial compound is geranyl-geranyl diphosphate (GGPP) that is synthesized from isopentenyl diphosphate and dimethylallyl diphosphate in terpenoid backbone biosynthesis.
The information about significant output compounds is provided in table 1.
Compound | Function |
---|---|
Beta-carotene | Energy transmission from chlorophyll Antioxidant |
Abscisic acid | Plant hormone Stress and pathogen response |
Lutein | Absorbtion of additional light Photoprotection Antioxidant |
Astaxanthin | Antioxidant |
This pathway is connected with terpenoid backbone synthesis at its start and with retinol metabolism in animals at beta-carotene.
The pathway in life domains
Three organisms from distinct domains were chosen (table 2) to study the carotenoid biosynthesis pathway.
Domain | Species | Lineage |
---|---|---|
Archaea | Sulfolobus solfactricus SULA | Crenarchaeota |
Bacteria | Streptomyces glaucescens | Actinobacteria |
Eukaryota | Arabidopsis thaliana | Plantae, Angiospermae |
Reactions specific to chosen organisms are shown in figures 2-4. All three organisms are able to synthesize lycopene from GGPP. The archaeon and the bacterium are unable to synthesize abscisic acid (as they do not need it) and have no direct connection from lycopene to lutein. The bacterium and the plant can synthesize beta-carotene and 7,8-dihydro-beta-carotene as well as the plant and the archaeon can synthesize astaxanthin. So, these organisms are able to execute some finished parts of the reference pathway.
Neurosporene desaturation in KEGG DB
The neurosporene desaturation (R04800) is the last step in lycopene biosynthesis (fig. 1) and carried out by zeta-carotene desaturase (EC1.3.5.6). The sceme of the reaction is provided in figure 5.