Biosynthetic origin of the isoprene units in chromenes of Piper aduncum (Piperaceae)


Autoria(s): Leite, Ana C.; Lopes, Adriana A.; Kato, Massuo J.; Bolzani, Vanderlan da Silva; Furlan, Maysa
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

27/05/2014

27/05/2014

01/12/2007

Resumo

Metabolic studies involving the incorporation of [1-13C]-D- glucose into intact leaves of Piper aduncum (Piperaceae) have indicated that both the mevalonate (MVA) and the pyruvate-triose (MEP) non-mevalonate pathways are implicated in the biosynthesis of isoprene moieties present in methyl 2,2-dimethyl-2H-1-chromene-6-carboxylate (1) and methyl 2,2-dimethyl-8- (3′-methyl-2′-butenyl)-2H-1-chromene-6-carboxylate (2). The pattern of incorporation of label from [1-13C]-D-glucose into these chromenes was determined by quantitative 13C NMR spectroscopy. The results confirmed that biosynthetic compartment of 1 and 2 could either be the plastid and/ or the cytosol or, possibly, an additional compartment such as the plastid inter-membrane space. ©2007 Sociedade Brasileira de Química.

Formato

1500-1503

Identificador

http://dx.doi.org/10.1590/S0103-50532007000800008

Journal of the Brazilian Chemical Society, v. 18, n. 8, p. 1500-1503, 2007.

0103-5053

1678-4790

http://hdl.handle.net/11449/70063

10.1590/S0103-50532007000800008

S0103-50532007000800008

WOS:000252859700008

2-s2.0-37549024189

2-s2.0-37549024189.pdf

Idioma(s)

eng

Relação

Journal of the Brazilian Chemical Society

Direitos

openAccess

Palavras-Chave #2-C-methyl-D-erythritol-4-phosphate pathway #[1-13C]-D-glucose #Chromenes #Mevalonate pathway #Piper aduncum
Tipo

info:eu-repo/semantics/article