Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa

Detalhes bibliográficos
Autor(a) principal: Vendruscolo, Raquel Guidetti
Data de Publicação: 2016
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000bxbn
Texto Completo: http://repositorio.ufsm.br/handle/1/11368
Resumo: The study of metabolism through the metabolites determination is assuming great importance in biological scientific scene, once it allows the knowledge or even understanding of how and why they are modified by existing routes in biological matrices. Microalgae are unicellular organisms prokaryotes or eukaryotes with photosynthetic capacity, that presents relatively simple requirements for growth and high potential to technological interest products synthesis. Thus, the aim of this study was to develop a simultaneous extraction method of non-polar fraction (fatty acids) and polar (amino acids and organic acids) in microalgae intracellular content, employing gas chromatography (GC) as analytical analysis tool. The compounds were extracted by Bligh e Dyer method with reducing the volume organic solvents and different forms of agitation and/or cell disruption. The non-polar compounds were derivatizated by Hatman e Lago method. The derivatization of polar compounds was performed according to Oms-oliu and validated for microalgae biomass sample, considering selectivity, linearity, detection and quantification limits, precision and accuracy. Then, were analyzed two chlorophytes, Chlorella vulgaris and Scenedesmus obliquus and two cyanobacteria, Aphanothece microscopica Nägeli and Phormidium autumnale. Eleven fatty acids, ten amino acids and three organic acids were detected between the species. The succinic, malic and citric acids, important intermediates from tricarboxylic acid cycle (TCA), from which are formed microalgae products of interest. Among the amino acids, the glutamic acid was the major compound in all species. Excepting the S. obliquus, the microalgae showed fatty acid profile mostly with saturated carbon chain. Posteriorly, the organic acids, amino acids and fatty acids were characterized during growth of S. obliquus microalgae cultivated photosynthetically with constant lighting. The succinic acid showed constant concentrations after 120 h of cultivation, while malic and citric acids had a significantly higher concentration to 336 h. Excepting the alanine, glutamic acid and asparagine, which showed peak in 336 h, the highest concentrations of amino acids were observed between 120 and 288 h. The fatty acid profile showed significant change between analysis of 0 to 120 h. Firstly the cultivation was characterized by the high concentration of saturated FA and short and medium chain compounds. After 120 h was detected higher concentration of unsaturated AG and long-chain (≥ 20 carbons). In this regard, it was possible establish relationship between microalgae biosynthetic pathways.
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spelling Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosaValidation and application method for microalgae metabolites determination using gas chromatographyAminoácidosÁcidos orgânicosÁcidos graxosDerivatizaçãoAmino acidsOrganic acidsFatty acidsDerivatizationCNPQ::CIENCIAS AGRARIAS::CIENCIA E TECNOLOGIA DE ALIMENTOSThe study of metabolism through the metabolites determination is assuming great importance in biological scientific scene, once it allows the knowledge or even understanding of how and why they are modified by existing routes in biological matrices. Microalgae are unicellular organisms prokaryotes or eukaryotes with photosynthetic capacity, that presents relatively simple requirements for growth and high potential to technological interest products synthesis. Thus, the aim of this study was to develop a simultaneous extraction method of non-polar fraction (fatty acids) and polar (amino acids and organic acids) in microalgae intracellular content, employing gas chromatography (GC) as analytical analysis tool. The compounds were extracted by Bligh e Dyer method with reducing the volume organic solvents and different forms of agitation and/or cell disruption. The non-polar compounds were derivatizated by Hatman e Lago method. The derivatization of polar compounds was performed according to Oms-oliu and validated for microalgae biomass sample, considering selectivity, linearity, detection and quantification limits, precision and accuracy. Then, were analyzed two chlorophytes, Chlorella vulgaris and Scenedesmus obliquus and two cyanobacteria, Aphanothece microscopica Nägeli and Phormidium autumnale. Eleven fatty acids, ten amino acids and three organic acids were detected between the species. The succinic, malic and citric acids, important intermediates from tricarboxylic acid cycle (TCA), from which are formed microalgae products of interest. Among the amino acids, the glutamic acid was the major compound in all species. Excepting the S. obliquus, the microalgae showed fatty acid profile mostly with saturated carbon chain. Posteriorly, the organic acids, amino acids and fatty acids were characterized during growth of S. obliquus microalgae cultivated photosynthetically with constant lighting. The succinic acid showed constant concentrations after 120 h of cultivation, while malic and citric acids had a significantly higher concentration to 336 h. Excepting the alanine, glutamic acid and asparagine, which showed peak in 336 h, the highest concentrations of amino acids were observed between 120 and 288 h. The fatty acid profile showed significant change between analysis of 0 to 120 h. Firstly the cultivation was characterized by the high concentration of saturated FA and short and medium chain compounds. After 120 h was detected higher concentration of unsaturated AG and long-chain (≥ 20 carbons). In this regard, it was possible establish relationship between microalgae biosynthetic pathways.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESO estudo do metabolismo, a partir da determinação de metabólitos, está assumindo elevada importância no cenário científico biológico, pois possibilita o conhecimento ou até mesmo o entendimento de como e porque são modificadas pelo meio as rotas existentes em matrizes biológicas. As microalgas são organismos unicelulares procariontes ou eucariontes com capacidade fotossintética, apresentam requisitos relativamente simples para o crescimento e elevado potencial para síntese de produtos de interesse tecnológico. Dessa forma, o objetivo deste trabalho foi desenvolver um método de extração simultânea da fração apolar (ácidos graxos) e polar (aminoácidos e ácidos orgânicos) do conteúdo intracelular de microalgas, empregando a cromatografia em fase gasosa (GC) como ferramenta analítica de análise. Os compostos foram extraídos pelo método de Bligh e Dyer com redução no volume de solventes orgânicos e diferentes formas de agitação e/ou ruptura celular. Os compostos apolares foram derivatizados segundo Hartman e Lago (1973). A derivatização dos compostos polares foi realizada de acordo com Oms-Oliu et al. (2011) e validada para a amostra biomassa microalgal quanto a seletividade, linearidade, limites de detecção e quantificação, precisão e exatidão. Então, foram analisadas duas clorofíceas, Chlorella vulgaris e Scenedesmus obliquus e duas cianobactérias, Aphanothece microscopica Nägeli e Phormidium autumnale. Foram detectados onze ácidos graxos, dez aminoácidos, e três ácidos orgânicos entre as espécies. Os ácidos succínico, málico e cítrico, importantes intermediários do ciclo do ácido tricarboxílico (TCA), a partir do qual são formados produtos microalgais de interesse. Dentre os aminoácidos, o ácido glutâmico foi o composto majoritário em todas espécies. Com exceção da S. obliquus, as microalgas apresentaram perfil de ácidos graxos (AG) majoritariamente de cadeia carbônica saturada. Posteriormente, foram caracterizados os ácidos orgânicos, os aminoácidos e os ácidos graxos ao longo do crescimento da microalga S. obliquus cultivada fotossinteticamente com iluminação constante. O ácido succínico apresentou concentrações constantes a partir das 120 h de cultivo, enquanto os ácidos málico e cítrico tiveram aumento significativo de concentração às 336 h. Com exceção da alanina, ácido glutâmico e asparagina que apresentaram ápice em 336 h, as maiores concentrações aminoácidos foram observadas entre 120 e 288 h. O perfil de ácidos graxos apresentou mudança significativa entre as análises de 0 e 120 h. Primeiramente o cultivo foi caracterizado pela elevada concentração de AG saturados e compostos de cadeia curta e média, a partir de 120 h foi detectado maior concentração de AG insaturados e de cadeia longa (≥ 20 carbonos). Em face disso, foi possível estabelecer relação entre vias biossintéticas das microalgas.Universidade Federal de Santa MariaBrasilCiência e Tecnologia dos AlimentosUFSMPrograma de Pós-Graduação em Ciência e Tecnologia dos AlimentosCentro de Ciências RuraisWagner, Rogerhttp://lattes.cnpq.br/4780821244553957Jacob-Lopes, Eduardohttp://lattes.cnpq.br/9203445906772879Vendruscolo, Raquel Guidetti2017-08-16T15:37:39Z2017-08-16T15:37:39Z2016-02-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/11368ark:/26339/001300000bxbnporAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2017-08-16T15:37:39Zoai:repositorio.ufsm.br:1/11368Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2017-08-16T15:37:39Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
Validation and application method for microalgae metabolites determination using gas chromatography
title Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
spellingShingle Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
Vendruscolo, Raquel Guidetti
Aminoácidos
Ácidos orgânicos
Ácidos graxos
Derivatização
Amino acids
Organic acids
Fatty acids
Derivatization
CNPQ::CIENCIAS AGRARIAS::CIENCIA E TECNOLOGIA DE ALIMENTOS
title_short Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
title_full Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
title_fullStr Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
title_full_unstemmed Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
title_sort Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
author Vendruscolo, Raquel Guidetti
author_facet Vendruscolo, Raquel Guidetti
author_role author
dc.contributor.none.fl_str_mv Wagner, Roger
http://lattes.cnpq.br/4780821244553957
Jacob-Lopes, Eduardo
http://lattes.cnpq.br/9203445906772879
dc.contributor.author.fl_str_mv Vendruscolo, Raquel Guidetti
dc.subject.por.fl_str_mv Aminoácidos
Ácidos orgânicos
Ácidos graxos
Derivatização
Amino acids
Organic acids
Fatty acids
Derivatization
CNPQ::CIENCIAS AGRARIAS::CIENCIA E TECNOLOGIA DE ALIMENTOS
topic Aminoácidos
Ácidos orgânicos
Ácidos graxos
Derivatização
Amino acids
Organic acids
Fatty acids
Derivatization
CNPQ::CIENCIAS AGRARIAS::CIENCIA E TECNOLOGIA DE ALIMENTOS
description The study of metabolism through the metabolites determination is assuming great importance in biological scientific scene, once it allows the knowledge or even understanding of how and why they are modified by existing routes in biological matrices. Microalgae are unicellular organisms prokaryotes or eukaryotes with photosynthetic capacity, that presents relatively simple requirements for growth and high potential to technological interest products synthesis. Thus, the aim of this study was to develop a simultaneous extraction method of non-polar fraction (fatty acids) and polar (amino acids and organic acids) in microalgae intracellular content, employing gas chromatography (GC) as analytical analysis tool. The compounds were extracted by Bligh e Dyer method with reducing the volume organic solvents and different forms of agitation and/or cell disruption. The non-polar compounds were derivatizated by Hatman e Lago method. The derivatization of polar compounds was performed according to Oms-oliu and validated for microalgae biomass sample, considering selectivity, linearity, detection and quantification limits, precision and accuracy. Then, were analyzed two chlorophytes, Chlorella vulgaris and Scenedesmus obliquus and two cyanobacteria, Aphanothece microscopica Nägeli and Phormidium autumnale. Eleven fatty acids, ten amino acids and three organic acids were detected between the species. The succinic, malic and citric acids, important intermediates from tricarboxylic acid cycle (TCA), from which are formed microalgae products of interest. Among the amino acids, the glutamic acid was the major compound in all species. Excepting the S. obliquus, the microalgae showed fatty acid profile mostly with saturated carbon chain. Posteriorly, the organic acids, amino acids and fatty acids were characterized during growth of S. obliquus microalgae cultivated photosynthetically with constant lighting. The succinic acid showed constant concentrations after 120 h of cultivation, while malic and citric acids had a significantly higher concentration to 336 h. Excepting the alanine, glutamic acid and asparagine, which showed peak in 336 h, the highest concentrations of amino acids were observed between 120 and 288 h. The fatty acid profile showed significant change between analysis of 0 to 120 h. Firstly the cultivation was characterized by the high concentration of saturated FA and short and medium chain compounds. After 120 h was detected higher concentration of unsaturated AG and long-chain (≥ 20 carbons). In this regard, it was possible establish relationship between microalgae biosynthetic pathways.
publishDate 2016
dc.date.none.fl_str_mv 2016-02-23
2017-08-16T15:37:39Z
2017-08-16T15:37:39Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/11368
dc.identifier.dark.fl_str_mv ark:/26339/001300000bxbn
url http://repositorio.ufsm.br/handle/1/11368
identifier_str_mv ark:/26339/001300000bxbn
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Ciência e Tecnologia dos Alimentos
UFSM
Programa de Pós-Graduação em Ciência e Tecnologia dos Alimentos
Centro de Ciências Rurais
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Ciência e Tecnologia dos Alimentos
UFSM
Programa de Pós-Graduação em Ciência e Tecnologia dos Alimentos
Centro de Ciências Rurais
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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