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1.
Plant Physiol ; 167(1): 89-101, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25406120

ABSTRACT

The esterification of methylecgonine (2-carbomethoxy-3ß-tropine) with benzoic acid is the final step in the biosynthetic pathway leading to the production of cocaine in Erythoxylum coca. Here we report the identification of a member of the BAHD family of plant acyltransferases as cocaine synthase. The enzyme is capable of producing both cocaine and cinnamoylcocaine via the activated benzoyl- or cinnamoyl-Coenzyme A thioesters, respectively. Cocaine synthase activity is highest in young developing leaves, especially in the palisade parenchyma and spongy mesophyll. These data correlate well with the tissue distribution pattern of cocaine as visualized with antibodies. Matrix-assisted laser-desorption ionization mass spectral imaging revealed that cocaine and cinnamoylcocaine are differently distributed on the upper versus lower leaf surfaces. Our findings provide further evidence that tropane alkaloid biosynthesis in the Erythroxylaceae occurs in the above-ground portions of the plant in contrast with the Solanaceae, in which tropane alkaloid biosynthesis occurs in the roots.


Subject(s)
Acyltransferases/metabolism , Cocaine/biosynthesis , Plant Proteins/metabolism , Catalysis , Cocaine/analogs & derivatives , Cocaine/analysis , Erythroxylaceae/enzymology , Erythroxylaceae/metabolism , Mesophyll Cells/enzymology , Mesophyll Cells/metabolism , Plant Leaves/enzymology , Plant Leaves/metabolism , Plant Proteins/chemistry
2.
Proc Natl Acad Sci U S A ; 109(26): 10304-9, 2012 Jun 26.
Article in English | MEDLINE | ID: mdl-22665766

ABSTRACT

The pharmacologically important tropane alkaloids have a scattered distribution among angiosperm families, like many other groups of secondary metabolites. To determine whether tropane alkaloids have evolved repeatedly in different lineages or arise from an ancestral pathway that has been lost in most lines, we investigated the tropinone-reduction step of their biosynthesis. In species of the Solanaceae, which produce compounds such as atropine and scopolamine, this reaction is known to be catalyzed by enzymes of the short-chain dehydrogenase/reductase family. However, in Erythroxylum coca (Erythroxylaceae), which accumulates cocaine and other tropane alkaloids, no proteins of the short-chain dehydrogenase/reductase family were found that could catalyze this reaction. Instead, purification of E. coca tropinone-reduction activity and cloning of the corresponding gene revealed that a protein of the aldo-keto reductase family carries out this reaction in E. coca. This protein, designated methylecgonone reductase, converts methylecgonone to methylecgonine, the penultimate step in cocaine biosynthesis. The protein has highest sequence similarity to other aldo-keto reductases, such as chalcone reductase, an enzyme of flavonoid biosynthesis, and codeinone reductase, an enzyme of morphine alkaloid biosynthesis. Methylecgonone reductase reduces methylecgonone (2-carbomethoxy-3-tropinone) stereospecifically to 2-carbomethoxy-3ß-tropine (methylecgonine), and has its highest activity, protein level, and gene transcript level in young, expanding leaves of E. coca. This enzyme is not found at all in root tissues, which are the site of tropane alkaloid biosynthesis in the Solanaceae. This evidence supports the theory that the ability to produce tropane alkaloids has arisen more than once during the evolution of the angiosperms.


Subject(s)
Alkaloids/biosynthesis , Erythroxylaceae/metabolism , Solanaceae/metabolism , Chromatography, Liquid , Molecular Sequence Data
3.
Int J Mol Sci ; 13(4): 4124-4140, 2012.
Article in English | MEDLINE | ID: mdl-22605969

ABSTRACT

In the study, we have examined the antitumor and antimicrobial activities of the methanol extract, the fractions, a fraction of total alkaloids and two alkaloids isolated from the stem of Erythroxylum caatingae Plowman. All test fractions, except the hexane fractions, showed antimicrobial activity on gram-positive bacteria and fungi. The acetate: methanol (95:5), acetate, chloroform and hexane fractions show the highest cytotoxicity activity against the NCI-H292, HEp-2 and K562 cell lines using MTT. The absence of hemolysis in the erythrocytes of mice was observed in these fractions and 6ß-Benzoyloxy-3α-(3,4,5- trimethoxybenzoyloxy) tropane (catuabine B). Staining with Annexin V-FITC and JC-1 was used to verify the mechanism of action of the compounds of E. caatingae that showed cytotoxicity less than 30 µg/mL in leukemic cells. After 48 h of incubation, we observed that the acetate: methanol (95:5), acetate, and chloroform fractions, as well as the catuabine B, increased in the number of cells in early apoptosis, from 53.0 to 74.8%. An analysis of the potential of the mitochondrial membrane by incorporation of JC-1 showed that most cells during incubation of the acetate: methanol (95:5) and acetate fractions (63.85 and 59.2%) were stained, suggesting the involvement of an intrinsic pathway of apoptosis.


Subject(s)
Anti-Infective Agents/pharmacology , Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Erythroxylaceae/metabolism , Plant Stems/metabolism , Alkaloids/isolation & purification , Alkaloids/pharmacology , Animals , Anti-Infective Agents/isolation & purification , Cell Line, Tumor , Cell Proliferation/drug effects , Cell Survival , Drug Discovery , Erythrocytes/drug effects , Female , Fungi/drug effects , Gram-Positive Bacteria/drug effects , Hemolysis/drug effects , Hep G2 Cells , Humans , Leukemia/drug therapy , Membrane Potential, Mitochondrial/drug effects , Mice , Microbial Sensitivity Tests , Mitochondrial Membranes/drug effects , Plant Extracts/pharmacology
4.
Plant Biol (Stuttg) ; 8(4): 430-8, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16917978

ABSTRACT

Young leaves are preferential targets for herbivores, and plants have developed different strategies to protect them. This study aimed to evaluate different leaf attributes of presumed relevance in protection against herbivory in four woody species (Erythroxylum argentinum, Lithrea brasiliensis, Myrciaria cuspidata, and Myrsine umbellata), growing in a dry restinga woodland in southern Brazil. Evaluation of leaf parameters was made through single-point sampling of leaves (leaf mass per area and leaf contents of nitrogen, carbon, and pigments) at three developmental stages and through time-course sampling of expanding leaves (area and strength). Leaves of M. umbellata showed the highest leaf mass per area (LMA), the largest area, and the longest expansion period. On the other extreme, Myrc. cuspidata had the smallest LMA and leaf size, and the shortest expansion period. Similarly to L. brasiliensis, it displayed red young leaves. None of the species showed delayed-greening, which might be related to the high-irradiance growth conditions. Nitrogen contents reduced with leaf maturity and reached the highest values in the young leaves of E. argentinum and Myrc. cuspidata and the lowest in M. umbellata. Each species seems to present a different set of protective attributes during leaf expansion. Myrciaria cuspidata appears to rely mostly on chemical defences to protect its soft leaves, and anthocyanins might play this role at leaf youth, while M. umbellata seems to invest more on mechanical defences, even at early stages of leaf growth, as well as on a low allocation of nitrogen to the leaves. The other species display intermediate characteristics.


Subject(s)
Plant Development , Plant Leaves/growth & development , Anacardiaceae/metabolism , Animals , Anthocyanins/metabolism , Brazil , Carbon/metabolism , Carotenoids/metabolism , Chlorophyll/metabolism , Erythroxylaceae/metabolism , Insecta/physiology , Myrtaceae/metabolism , Nitrogen/metabolism , Plant Leaves/metabolism , Plant Leaves/parasitology , Plants/metabolism , Plants/parasitology , Primulaceae/metabolism , Time Factors
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