作者: Bilal Camara , Odette Dogbo , Alain d'Harlingue , Hans Kleinig , René Monéger
DOI: 10.1016/0005-2760(85)90074-8
关键词: Biochemistry 、 Cofactor 、 Mersalyl 、 Metabolism 、 Lycopene 、 Membrane 、 Chromoplast membrane 、 Chromoplast 、 Neurosporene 、 Chemistry
摘要: Abstract The cyclization of lycopene to β,β-carotene (β-carotene) was studied using chromoplast membranes prepared from Capsicum fruits. enzymic activity is tightly bound the and, under optimal conditions, cyclized β-carotene without accumulation intermediate β,ψ-carotene (γ-carotene). In this system, no formation (6,R)-β,ϵ-carotene (α-carotene) occurs. pH for 6.8. Nucleotide cofactors are not required activity. stimulated in presence Tween 80 contrast inhibitory effect Triton X-100. Thiol reagents such as mersalyl, N-ethylmaleimide and p-chloromercuribenzoate strongly inhibit β-carotene. Octyldiethylamine dodecyl diethylamine potent inhibitors cyclase membranes.