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Construction of a pathway to C50-?-carotene.


ABSTRACT: Substrate tolerance of bacterial cyclases has been demonstrated in various contexts, but little is known about that of plant cyclases. Here, we tested two plant ?-cyclases to convert C50-lycopene, which we previously established by rounds of directed evolution. Unlike bacterial ?-cyclases, two-end cyclase from lettuce exhibited complete specificity against this molecule, indicating that this enzyme has some mechanism that exerts size-specificity. Arabidopsis one-end cyclase At-y2 showed detectable activity to C50-lycopene. Interestingly, we found that it functions as a two-end cyclase in a C50 context. Based on this observation, a possible model for substrate discrimination of this enzyme is proposed.

SUBMITTER: Otani Y 

PROVIDER: S-EPMC6516660 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Construction of a pathway to C50-ε-carotene.

Otani Yusuke Y   Maoka Takashi T   Kawai-Noma Shigeko S   Saito Kyoichi K   Umeno Daisuke D  

PloS one 20190514 5


Substrate tolerance of bacterial cyclases has been demonstrated in various contexts, but little is known about that of plant cyclases. Here, we tested two plant ε-cyclases to convert C50-lycopene, which we previously established by rounds of directed evolution. Unlike bacterial β-cyclases, two-end cyclase from lettuce exhibited complete specificity against this molecule, indicating that this enzyme has some mechanism that exerts size-specificity. Arabidopsis one-end cyclase At-y2 showed detectab  ...[more]

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2016-09-14 | GSE86866 | GEO