Genetically engineered biosynthetic pathways for nonnatural C60 carotenoids using C5-elongases and C50-cyclases in Escherichia coli
Genetically engineered biosynthetic pathways for nonnatural C60 carotenoids using C5-elongases and C50-cyclases in Escherichia coli
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DOI:
10.1038/s41598-019-39289-w
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发表时间:
2019-02-27
影响因子:
4.6
通讯作者:
Umeno, Daisuke
中科院分区:
文献类型:
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作者:
Li, Ling;Furubayashi, Maiko;Umeno, Daisuke
While the majority of the natural carotenoid pigments are based on 40-carbon (C-40) skeleton, some carotenoids from bacteria have larger C-50 skeleton, biosynthesized by attaching two isoprene units (C-5) to both sides of the C-40 carotenoid pigment lycopene. Subsequent cyclization reactions result in the production of C-50 carotenoids with diverse and unique skeletal structures. To produce even larger nonnatural novel carotenoids with C-50 + C-5 + C-5 = C-60 skeletons, we systematically coexpressed natural C-50 carotenoid biosynthetic enzymes (lycopene C-5-elongases and C-50-cyclases) from various bacterial sources together with the laboratory-engineered nonnatural C-50-lycopene pathway in Escherichia coli. Among the tested enzymes, the elongases and cyclases from Micrococcus luteus exhibited significant activity toward C-50-lycopene, and yielded the novel carotenoids C-60-flavuxanthin and C-60-sarcinaxanthin. Moreover, coexpression of M. luteus elongase with Corynebacterium cyclase resulted in the production of C-60-sarcinaxanthin, C-60-sarprenoxanthin, and C-60-decaprenoxanthin.