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1.
Science ; 379(6638): 1252-1264, 2023 03 24.
Artigo em Inglês | MEDLINE | ID: mdl-36952412

RESUMO

The Chilean soapbark tree (Quillaja saponaria) produces soap-like molecules called QS saponins that are important vaccine adjuvants. These highly valuable compounds are sourced by extraction from the bark, and their biosynthetic pathway is unknown. Here, we sequenced the Q. saponaria genome. Through genome mining and combinatorial expression in tobacco, we identified 16 pathway enzymes that together enable the production of advanced QS pathway intermediates that represent a bridgehead for adjuvant bioengineering. We further identified the enzymes needed to make QS-7, a saponin with excellent therapeutic properties and low toxicity that is present in low abundance in Q. saponaria bark extract. Our results enable the production of Q. saponaria vaccine adjuvants in tobacco and open the way for new routes to access and engineer natural and new-to-nature immunostimulants.


Assuntos
Adjuvantes de Vacinas , Vias Biossintéticas , Quillaja , Saponinas , Adjuvantes de Vacinas/biossíntese , Adjuvantes de Vacinas/química , Adjuvantes de Vacinas/genética , Quillaja/enzimologia , Quillaja/genética , Saponinas/biossíntese , Saponinas/química , Saponinas/genética , Análise de Sequência de DNA , Genoma de Planta , Vias Biossintéticas/genética , Nicotiana/genética , Nicotiana/metabolismo , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo
2.
Nat Commun ; 12(1): 2563, 2021 05 07.
Artigo em Inglês | MEDLINE | ID: mdl-33963185

RESUMO

Non-random gene organization in eukaryotes plays a significant role in genome evolution. Here, we investigate the origin of a biosynthetic gene cluster for production of defence compounds in oat-the avenacin cluster. We elucidate the structure and organisation of this 12-gene cluster, characterise the last two missing pathway steps, and reconstitute the entire pathway in tobacco by transient expression. We show that the cluster has formed de novo since the divergence of oats in a subtelomeric region of the genome that lacks homology with other grasses, and that gene order is approximately colinear with the biosynthetic pathway. We speculate that the positioning of the late pathway genes furthest away from the telomere may mitigate against a 'self-poisoning' scenario in which toxic intermediates accumulate as a result of telomeric gene deletions. Our investigations reveal a striking example of adaptive evolution underpinned by remarkable genome plasticity.


Assuntos
Avena/genética , Resistência à Doença/genética , Redes e Vias Metabólicas/genética , Telômero/genética , Avena/metabolismo , Grão Comestível/genética , Evolução Molecular , Sequenciamento de Nucleotídeos em Larga Escala , Hibridização in Situ Fluorescente , Família Multigênica , RNA-Seq , Sequências Repetitivas de Ácido Nucleico , Saponinas/biossíntese , Saponinas/química , Saponinas/genética , Sintenia/genética , Nicotiana/metabolismo , Sequenciamento Completo do Genoma
3.
Proc Natl Acad Sci U S A ; 116(52): 27105-27114, 2019 Dec 26.
Artigo em Inglês | MEDLINE | ID: mdl-31806756

RESUMO

Plants produce an array of natural products with important ecological functions. These compounds are often decorated with oligosaccharide groups that influence bioactivity, but the biosynthesis of such sugar chains is not well understood. Triterpene glycosides (saponins) are a large family of plant natural products that determine important agronomic traits, as exemplified by avenacins, antimicrobial defense compounds produced by oats. Avenacins have a branched trisaccharide moiety consisting of l-arabinose linked to 2 d-glucose molecules that is critical for antifungal activity. Plant natural product glycosylation is usually performed by uridine diphosphate-dependent glycosyltransferases (UGTs). We previously characterized the arabinosyltransferase that initiates the avenacin sugar chain; however, the enzymes that add the 2 remaining d-glucose molecules have remained elusive. Here we characterize the enzymes that catalyze these last 2 glucosylation steps. AsUGT91G16 is a classical cytosolic UGT that adds a 1,2-linked d-glucose molecule to l-arabinose. Unexpectedly, the enzyme that adds the final 1,4-linked d-glucose (AsTG1) is not a UGT, but rather a sugar transferase belonging to Glycosyl Hydrolase family 1 (GH1). Unlike classical UGTs, AsTG1 is vacuolar. Analysis of oat mutants reveals that AsTG1 corresponds to Sad3, a previously uncharacterized locus shown by mutation to be required for avenacin biosynthesis. AsTG1 and AsUGT91G16 form part of the avenacin biosynthetic gene cluster. Our demonstration that a vacuolar transglucosidase family member plays a critical role in triterpene biosynthesis highlights the importance of considering other classes of carbohydrate-active enzymes in addition to UGTs as candidates when elucidating pathways for the biosynthesis of glycosylated natural products in plants.

4.
Artigo em Inglês | MEDLINE | ID: mdl-31235546

RESUMO

Glycosylation plays a major role in the structural diversification of plant natural products. It influences the properties of molecules by modifying the reactivity and solubility of the corresponding aglycones, so influencing cellular localization and bioactivity. Glycosylation of plant natural products is usually carried out by uridine diphosphate(UDP)-dependent glycosyltransferases (UGTs) belonging to the carbohydrate-active enzyme glycosyltransferase 1 (GT1) family. These enzymes transfer sugars from UDP-activated sugar moieties to small hydrophobic acceptor molecules. Plant GT1s generally show high specificity for their sugar donors and recognize a single UDP sugar as their substrate. In contrast, they are generally promiscuous with regard to acceptors, making them attractive biotechnological tools for small molecule glycodiversification. Although microbial hosts have traditionally been used for heterologous engineering of plant-derived glycosides, transient plant expression technology offers a potentially disruptive platform for rapid characterization of new plant glycosyltransferases and biosynthesis of complex glycosides.


Assuntos
Glicosiltransferases/metabolismo , Plantas/metabolismo , Difosfato de Uridina/metabolismo , Biocatálise , Produtos Biológicos/metabolismo , Glicosilação , Glicosiltransferases/química , Glicosiltransferases/classificação , Filogenia , Plantas/enzimologia , Conformação Proteica
5.
Plant Cell ; 30(12): 3038-3057, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30429223

RESUMO

Glycosylation of small molecules is critical for numerous biological processes in plants, including hormone homeostasis, neutralization of xenobiotics, and synthesis and storage of specialized metabolites. Glycosylation of plant natural products is usually performed by uridine diphosphate-dependent glycosyltransferases (UGTs). Triterpene glycosides (saponins) are a large family of plant natural products that determine important agronomic traits such as disease resistance and flavor and have numerous pharmaceutical applications. Most characterized plant natural product UGTs are glucosyltransferases, and little is known about enzymes that add other sugars. Here we report the discovery and characterization of AsAAT1 (UGT99D1), which is required for biosynthesis of the antifungal saponin avenacin A-1 in oat (Avena strigosa). This enzyme adds l-Ara to the triterpene scaffold at the C-3 position, a modification critical for disease resistance. The only previously reported plant natural product arabinosyltransferase is a flavonoid arabinosyltransferase from Arabidopsis (Arabidopsis thaliana). We show that AsAAT1 has high specificity for UDP-ß-l-arabinopyranose, identify two amino acids required for sugar donor specificity, and through targeted mutagenesis convert AsAAT1 into a glucosyltransferase. We further identify a second arabinosyltransferase potentially implicated in the biosynthesis of saponins that determine bitterness in soybean (Glycine max). Our investigations suggest independent evolution of UDP-Ara sugar donor specificity in arabinosyltransferases in monocots and eudicots.


Assuntos
Glicosiltransferases/metabolismo , Pentosiltransferases/metabolismo , Arabidopsis/genética , Arabidopsis/metabolismo , Proteínas de Arabidopsis/genética , Proteínas de Arabidopsis/metabolismo , Avena/genética , Avena/metabolismo , Glicosiltransferases/genética , Pentosiltransferases/genética , Saponinas/metabolismo , Triterpenos/metabolismo , Açúcares de Uridina Difosfato/genética , Açúcares de Uridina Difosfato/metabolismo
6.
Annu Rev Plant Biol ; 65: 225-57, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24498976

RESUMO

The triterpenes are one of the most numerous and diverse groups of plant natural products. They are complex molecules that are, for the most part, beyond the reach of chemical synthesis. Simple triterpenes are components of surface waxes and specialized membranes and may potentially act as signaling molecules, whereas complex glycosylated triterpenes (saponins) provide protection against pathogens and pests. Simple and conjugated triterpenes have a wide range of applications in the food, health, and industrial biotechnology sectors. Here, we review recent developments in the field of triterpene biosynthesis, give an overview of the genes and enzymes that have been identified to date, and discuss strategies for discovering new triterpene biosynthetic pathways.


Assuntos
Plantas/metabolismo , Triterpenos/metabolismo , Vias Biossintéticas , Plantas/enzimologia , Plantas/genética , Saponinas/biossíntese , Saponinas/metabolismo
7.
Bioorg Med Chem ; 21(16): 4762-7, 2013 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-23806835

RESUMO

In connection with prospective (18)F-PET imaging studies, the potential for enzymatic synthesis of fluorine-labelled glycosides of small molecules was investigated. Approaches to the enzymatic synthesis of anomeric phosphates of d-gluco-configured fluorosugars proved ineffective. In contrast, starting in the d-galacto series and relying on the consecutive action of Escherichia coli galactokinase (GalK), galactose-1-phosphate uridylyltransferase (GalPUT), uridine-5'-diphosphogalactose 4-epimerase (GalE) and oat root glucosyltransferase (SAD10), a quick and effective synthesis of 6-deoxy-6-fluoro-d-glucosyl N-methylanthranilate ester was achieved.


Assuntos
Proteínas de Escherichia coli/metabolismo , Galactoquinase/metabolismo , Glucosídeos/química , Glucosiltransferases/metabolismo , Proteínas de Plantas/metabolismo , UTP-Hexose-1-Fosfato Uridililtransferase/metabolismo , ortoaminobenzoatos/química , ortoaminobenzoatos/metabolismo , Avena/enzimologia , Escherichia coli/enzimologia , Glucosídeos/metabolismo
8.
Plant Cell ; 25(3): 1078-92, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23532069

RESUMO

Operon-like gene clusters are an emerging phenomenon in the field of plant natural products. The genes encoding some of the best-characterized plant secondary metabolite biosynthetic pathways are scattered across plant genomes. However, an increasing number of gene clusters encoding the synthesis of diverse natural products have recently been reported in plant genomes. These clusters have arisen through the neo-functionalization and relocation of existing genes within the genome, and not by horizontal gene transfer from microbes. The reasons for clustering are not yet clear, although this form of gene organization is likely to facilitate co-inheritance and co-regulation. Oats (Avena spp) synthesize antimicrobial triterpenoids (avenacins) that provide protection against disease. The synthesis of these compounds is encoded by a gene cluster. Here we show that a module of three adjacent genes within the wider biosynthetic gene cluster is required for avenacin acylation. Through the characterization of these genes and their encoded proteins we present a model of the subcellular organization of triterpenoid biosynthesis.


Assuntos
Avena/genética , Genes de Plantas , Família Multigênica , Saponinas/metabolismo , Triterpenos/metabolismo , Acilação , Aciltransferases/classificação , Aciltransferases/genética , Aciltransferases/metabolismo , Sequência de Aminoácidos , Antifúngicos/metabolismo , Antifúngicos/farmacologia , Ascomicetos/patogenicidade , Avena/enzimologia , Avena/metabolismo , Regulação da Expressão Gênica de Plantas , Metilação , Metiltransferases/classificação , Metiltransferases/genética , Metiltransferases/metabolismo , Dados de Sequência Molecular , Mutação , Filogenia , Doenças das Plantas/microbiologia , Proteínas de Plantas/classificação , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Raízes de Plantas/genética , Raízes de Plantas/metabolismo , Saponinas/genética , Relação Estrutura-Atividade , Nicotiana/genética , Nicotiana/metabolismo
9.
J Biol Chem ; 288(6): 3696-704, 2013 Feb 08.
Artigo em Inglês | MEDLINE | ID: mdl-23258535

RESUMO

Plants produce a huge array of specialized metabolites that have important functions in defense against biotic and abiotic stresses. Many of these compounds are glycosylated by family 1 glycosyltransferases (GTs). Oats (Avena spp.) make root-derived antimicrobial triterpenes (avenacins) that provide protection against soil-borne diseases. The ability to synthesize avenacins has evolved since the divergence of oats from other cereals and grasses. The major avenacin, A-1, is acylated with N-methylanthranilic acid. Previously, we have cloned and characterized three genes for avenacin synthesis (for the triterpene synthase SAD1, a triterpene-modifying cytochrome P450 SAD2, and the serine carboxypeptidase-like acyl transferase SAD7), which form part of a biosynthetic gene cluster. Here, we identify a fourth member of this gene cluster encoding a GT belonging to clade L of family 1 (UGT74H5), and show that this enzyme is an N-methylanthranilic acid O-glucosyltransferase implicated in the synthesis of avenacin A-1. Two other closely related family 1 GTs (UGT74H6 and UGT74H7) are also expressed in oat roots. One of these (UGT74H6) is able to glucosylate both N-methylanthranilic acid and benzoic acid, whereas the function of the other (UGT74H7) remains unknown. Our investigations indicate that UGT74H5 is likely to be key for the generation of the activated acyl donor used by SAD7 in the synthesis of the major avenacin, A-1, whereas UGT74H6 may contribute to the synthesis of other forms of avenacin that are acylated with benzoic acid.


Assuntos
Avena/enzimologia , Regulação Enzimológica da Expressão Gênica/fisiologia , Regulação da Expressão Gênica de Plantas/fisiologia , Glicosiltransferases/biossíntese , Proteínas de Plantas/metabolismo , Raízes de Plantas/enzimologia , Saponinas/metabolismo , Acilação/fisiologia , Avena/genética , Sistema Enzimático do Citocromo P-450/genética , Sistema Enzimático do Citocromo P-450/metabolismo , Glicosiltransferases/genética , Família Multigênica/fisiologia , Proteínas de Plantas/genética , Raízes de Plantas/genética , Saponinas/genética
10.
FEBS J ; 278(2): 390-400, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21166996

RESUMO

The volatile compounds that constitute the fruit aroma of ripe tomato (Solanum lycopersicum) are often sequestered in glycosylated form. A homology-based screen was used to identify the gene SlUGT5, which is a member of UDP-glycosyltransferase 72 family and shows specificity towards a range of substrates, including flavonoid, flavanols, hydroquinone, xenobiotics and chlorinated pollutants. SlUGT5 was shown to be expressed primarily in ripening fruit and flowers, and mapped to chromosome I in a region containing a QTL that affected the content of guaiacol and eugenol in tomato crosses. Recombinant SlUGT5 protein demonstrated significant activity towards guaiacol and eugenol, as well as benzyl alcohol and methyl salicylate; however, the highest in vitro activity and affinity was shown for hydroquinone and salicyl alcohol. NMR analysis identified isosalicin as the only product of salicyl alcohol glycosylation. Protein modelling and substrate docking analysis were used to assess the basis for the substrate specificity of SlUGT5. The analysis correctly predicted the interactions with SlUGT5 substrates, and also indicated that increased hydrogen bonding, due to the presence of a second hydrophilic group in methyl salicylate, guaiacol and hydroquinone, appeared to more favourably anchor these acceptors within the glycosylation site, leading to increased stability, higher activities and higher substrate affinities.


Assuntos
Glicosiltransferases/metabolismo , Fenóis/metabolismo , Proteínas de Plantas/metabolismo , Solanum lycopersicum/enzimologia , Compostos Orgânicos Voláteis/metabolismo , Sequência de Aminoácidos , Álcool Benzílico/química , Álcool Benzílico/metabolismo , Álcoois Benzílicos/química , Álcoois Benzílicos/metabolismo , Domínio Catalítico/fisiologia , Cromossomos/genética , Clonagem Molecular , Escherichia coli/genética , Escherichia coli/metabolismo , Eugenol/química , Eugenol/metabolismo , Expressão Gênica/genética , Glicosiltransferases/química , Glicosiltransferases/genética , Guaiacol/química , Guaiacol/metabolismo , Ligação de Hidrogênio , Hidroquinonas/química , Hidroquinonas/metabolismo , Solanum lycopersicum/genética , Modelos Moleculares , Dados de Sequência Molecular , Álcool Feniletílico/química , Álcool Feniletílico/metabolismo , Filogenia , Proteínas de Plantas/química , Proteínas de Plantas/genética , Estruturas Vegetais/metabolismo , Proteínas Recombinantes/genética , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/metabolismo , Salicilatos/química , Salicilatos/metabolismo , Homologia de Sequência de Aminoácidos , Especificidade por Substrato/fisiologia , Uridina Difosfato Glucose/metabolismo
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