Validação e aplicação de método para determinação de metabólitos microalgais empregando cromatografia em fase gasosa
Autor(a) principal: | |
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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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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 |
_version_ |
1815172318823972864 |