Arabidopsis thaliana lines overexpressing the Chlamydomonas reinhardtii beta-carotene ketolase BKT accumulate high amounts of astaxanthin in the leaves. 1633 and 1722 genes are differentially expressed in the leaves and siliques, respectively, of BKT-overexpressing plants. These genes are enriched in the carotenoid biosynthetic pathways, and plant hormone biosynthesis and signaling pathways. As compared to the wild-type leaves and siliques, overexpression of BKT increases the levels of most amino acids, but decreases the contents of sugars and carbohydrates. Overexpressing plants have lower sensitivity to abscisic acid and increased tolerance to oxidative stress, and also exhibit enhanced resistance to the pathogen Pseudomonas syringae pv. tomato DC3000
engineering the ketocarotenoid pathway into Chlamydomonas haploid vegetative green cells instead of the diploid zygospore stage by overexpressing beta-carotene ketolase. Overexpression results in the production of canthaxanthin, as well as a drastic reduction in the chlorophyll concentration. These phenotypes can only be detected from lines transformed and grown heterotrophically in the dark. Once exposed to light, these transformants lose their phenotypes as well as their antibiotic resistance
transgenic Arabidopsis thaliana expressing the beta-carotene ketolase from Chlamydomonas reinhardtii develop orange leaves which accumulate astaxanthin up to 2 mg/g dry weight with a 1.8fold increase in total carotenoids. The ketolases with high activity of converting zeaxanthin to astaxanthin triggers transgenic Arabidopsis to accumulate large amounts of astaxanthin in leaves and seeds
transgenic Arabidopsis thaliana expressing the beta-carotene ketolase from Chlamydomonas reinhardtii develop orange leaves which accumulate astaxanthin up to 2 mg/g dry weight with a 1.8fold increase in total carotenoids. The ketolases with high activity of converting zeaxanthin to astaxanthin triggers transgenic Arabidopsis to accumulate large amounts of astaxanthin in leaves and seeds
transgenic Arabidopsis thaliana expressing the beta-carotene ketolase from Chlamydomonas reinhardtii develop orange leaves which accumulate astaxanthin up to 2 mg/g dry weight with a 1.8fold increase in total carotenoids. The ketolases with high activity of converting zeaxanthin to astaxanthin triggers transgenic Arabidopsis to accumulate large amounts of astaxanthin in leaves and seeds
bioengineering of astaxanthin biosynthesis in rice endosperm. Transgenic overexpression of phytoene synthase and phytoene desaturase, of phytoene synthase, phytoene desaturase, zeaxanthin 4-ketolase, and all four genes phytoene synthase, phytoene desaturase, beta-carotene ketolase, and zeaxanthin hydroxylase driven by rice endosperm-specific promoters establish the carotenoid/ketocarotenoid/astaxanthin biosynthetic pathways in the endosperm and result in various types of germplasm, from yellow-grained beta-carotene-enriched Golden Rice to orange-red-grained Canthaxanthin Rice and Astaxanthin Rice, respectively. Grains of Astaxanthin Rice are enriched with astaxanthin in the endosperm and have higher antioxidant activity
bioengineering of astaxanthin biosynthesis in rice endosperm. Transgenic overexpression of phytoene synthase and phytoene desaturase, of phytoene synthase, phytoene desaturase, zeaxanthin 4-ketolase, and all four genes phytoene synthase, phytoene desaturase, beta-carotene ketolase, and zeaxanthin hydroxylase driven by rice endosperm-specific promoters establish the carotenoid/ketocarotenoid/astaxanthin biosynthetic pathways in the endosperm and result in various types of germplasm, from yellow-grained beta-carotene-enriched Golden Rice to orange-red-grained Canthaxanthin Rice and Astaxanthin Rice, respectively. Grains of Astaxanthin Rice are enriched with astaxanthin in the endosperm and have higher antioxidant activity
engineering the ketocarotenoid pathway into Chlamydomonas haploid vegetative green cells instead of the diploid zygospore stage by overexpressing beta-carotene ketolase. Overexpression results in the production of canthaxanthin, as well as a drastic reduction in the chlorophyll concentration. These phenotypes can only be detected from lines transformed and grown heterotrophically in the dark. Once exposed to light, these transformants lose their phenotypes as well as their antibiotic resistance
Functional characterization of various algal carotenoid ketolases reveals that ketolating zeaxanthin efficiently is essential for high production of astaxanthin in transgenic Arabidopsis