One ring or two? Determination of ring number in carotenoids by lycopene «-cyclases
نویسندگان
چکیده
Carotenoids in the photosynthetic membranes of plants typically contain two b-rings (e.g., b-carotene and zeaxanthin) or one «and one b-ring (e.g., lutein). Carotenoids with two «-rings are uncommon. We reported earlier that the Arabidopsis thaliana lycopene «-cyclase (LCYe) adds one «-ring to the symmetrical linear substrate lycopene, whereas the structurally related lycopene b-cyclase (LCYb) adds two b-rings. Here we describe a cDNA encoding LCYe in romaine lettuce (Lactuca sativa var. romaine), one of the few plant species known to accumulate substantial quantities of a carotenoid with two «-rings: lactucaxanthin. The product of the lettuce cDNA, similar in sequence to the Arabidopsis LCYe (77% amino acid identity), efficiently converted lycopene into the bicyclic «-carotene in a heterologous Escherichia coli system. Regions of the lettuce and Arabidopsis «-cyclases involved in the determination of ring number were mapped by analysis of chimeric «-cyclases constructed by using an inverse PCR approach. A single amino acid was found to act as a molecular switch: lettuce LCYe mutant H457L added only one «-ring to lycopene, whereas the complementary Arabidopsis LCYe mutant, L448H, added two «-rings. An R residue in this position also yields a bi-«-cyclase for both the lettuce and Arabidopsis enzymes. Construction and analysis of chimera of related enzymes with differing catalytic activities provide an informative approach that may be of particular utility for studying membrane-associated enzymes that cannot easily be crystallized or modeled to existing crystal structures.
منابع مشابه
Cloning and Functional Characterization of a Lycopene β-Cyclase from Macrophytic Red Alga Bangia fuscopurpurea
Lycopene cyclases cyclize the open ends of acyclic lycopene (ψ,ψ-carotene) into β- or ε-ionone rings in the crucial bifurcation step of carotenoid biosynthesis. Among all carotenoid constituents, β-carotene (β,β-carotene) is found in all photosynthetic organisms, except for purple bacteria and heliobacteria, suggesting a ubiquitous distribution of lycopene β-cyclase activity in these organisms....
متن کاملIdentification of a fourth family of lycopene cyclases in photosynthetic bacteria.
A fourth and large family of lycopene cyclases was identified in photosynthetic prokaryotes. The first member of this family, encoded by the cruA gene of the green sulfur bacterium Chlorobium tepidum, was identified in a complementation assay with a lycopene-producing strain of Escherichia coli. Orthologs of cruA are found in all available green sulfur bacterial genomes and in all cyanobacteria...
متن کاملMolecular evolution of lycopene cyclases involved in the formation of carotenoids with ionone end groups.
A survey is given of the lycopene cyclase genes present in bacteria, fungi and plants where two completely unrelated types exist. One is the classical monomeric bacterial beta-cyclase gene, crtY, which may be an ancestor of crtL, the gene for a beta-cyclase in cyanobacteria. From crtL a line of evolution can be drawn to plant beta- and epsilon-cyclase genes and to the gene of capsanthin/capsoru...
متن کاملDefining the primary route for lutein synthesis in plants: The role of Arabidopsis carotenoid -ring hydroxylase CYP97A3
Lutein, a dihydroxy derivative of -carotene ( , -carotene), is the most abundant carotenoid in photosynthetic plant tissues where it plays important roles in light-harvesting complex-II structure and function. The synthesis of lutein from lycopene requires at least four distinct enzymatic reactions: and -ring cyclizations and hydroxylation of each ring at the C-3 position. Three carotenoid hydr...
متن کاملSll0254 (CrtL(diox)) is a bifunctional lycopene cyclase/dioxygenase in cyanobacteria producing myxoxanthophyll.
Upon depletion of Sll0254 in Synechocystis sp. strain PCC 6803, cyclized carotenoids were replaced by linear, relatively hydrophilic carotenoids, and the amount of the two photosystems decreased greatly. Full segregants of the sll0254 deletion in Synechocystis were not obtained, implying that this gene is essential for survival, most likely to allow normal cell division. The N-terminal half of ...
متن کامل