ABSTRACT
This study aimed to screen purple non-sulfur bacteria capable of accumulating granules or polyhydroxybutyrate (PHB) inside the cells, identify the potent strain, assay the enzyme or PHA synthase, and compare the PHB synthase gene with that of related strains. A total of 58 strains of purple non-sulfur bacteria were isolated from 108 samples of chicken feces in the chicken-egg farm of the Department of Animal Science, Faculty of Natural Resources at Prince of Songkla University, Hat Yai, Thailand. After cultivating the bacteria in glutamate malate (GM) medium without added glutamic acid under light (3,000 Lux) at 35oC for 5 days, the intracellular biopolymer granules of the bacteria were observed by using a Confocal Laser Scanning Microscope (CLSM) with excitation and emission wavelength of 530 and 605 nm, respectively. Gas chromatography (GC) was carried out for quantitative analysis of PHB. There were five strains, CH12, CH52, CH72, CH90 and CH92, showed biopolymer granules under CLSM, and accumulated PHB 5, 1.7, 1.5, 1.4 and 1.8% (w w-1) of the cell dry weight (CDW), respectively. The 16S rDNA sequence analysis of CH12 strain showed a high homology of 100% correlation to that of Rhodopseudomonas palustris strain NCIB8288. Regarding the taxonomic characteristics and 16S rDNA sequence analysis, CH12 strain was identified as Rps. palustris NCIB8288. The PHA synthase activity of the crude extract from CH12 strain was 25 units/mL. The conserved regions could be aligned and selected among 5 strains of Rhodopseudomonas palustris (strains BisA53, TIE-1, CGA009, HaA2 and BisB18). The purified PCR product was obtained for further studies.
Este estudo teve como objetivo rastrear bactérias púrpuras não sulfurosas capazes de acumular grânulos ou polihidroxibutirato (PHB) dentro das células, identificar a estirpe potente, ensaiar a enzima ou PHA sintaxe, e comparar com o gene PHB sintase com aquele de estirpes relacionadas. Um total de 58 estirpes de bactérias púrpuras não sulfurosas foram isoladas a partir de 108 amostras de fezes de galinhas na granja produtora de ovos do Departamento de Ciência Animal, Faculdade de Recursos Naturais da Universidade Prince of Songkla, Hat Yai, Tailândia. Depois de cultivar as bactérias em um substrato de glutamato/malato (GM), sem ácido glutâmico adicionado, sob luz (3000 lux) a 35 ºC durante 5 dias, os grânulos de biopolímeros intracelulares das bactérias foram observados utilizando um microscópio confocal (do inglês Confocal Laser Scanning Microscope - CLSM) com comprimentos de onda de excitação e emissão de 530 e 605 nm, respectivamente. A cromatografia gasosa (do inglês Gas chromatography - GC) foi realizada para uma análise quantitativa de PHB. Havia 5 estirpes, CH12, CH52, CH72, CH90 e CH92, que mostraram grânulos biopoliméricos quando submetidos ao CLSM, e PHB-5 acumulado de 1.7, 1.5, 1.4 and 1.8% (w w-1) do peso celular seco (do inglês cell dry weight - CDW), respectivamente. A análise da sequência do rDNA 16S da estirpe CH12 demonstrou uma alta correlação de homologia de 100% para aquela da estirpe NCIB8288 da Rhodopseudomonas palustris. Em relação às características taxonômicas e da análise da sequência do rDNA 16S, a estirpe CH12 foi identificada como Rps. palustris NCIB8288. A atividade da PHA sintase do extrato bruto da estirpe CH12 foi de 25 unidades/mL. As regiões conservadas puderam ser alinhadas e selecionadas entre 5 estirpes de Rhodopseudomonas palustris (BisA53, TIE-1, CGA009, HaA2 e BisB18). O produto purificado da reação em cadeia da polimerase - PCR foi obtido para estudos futuros.
Subject(s)
Rhodospirillaceae , Chickens , Feces , GenesABSTRACT
Los Polihidroxialcanoatos (PHAs) son biopolímeros con características similares a los plásticos sintéticos, pero rápidamente biodegradables dado su origen microbiano. En esta investigación se aislaron 248 colonias bacteriales de suelos contaminados con residuos del beneficio de fique en Guarne (Antioquia), evaluándose su capacidad como productoras de PHAs. Se realizaron tinciones con rojo y azul de Nilo y detección por PCR del gen PhaC. Las bacterias positivas a dichas pruebas, fueron identificadas utilizando análisis filogenético de secuencias de 16S del ADNr y pruebas bioquímicas. Finalmente, se evaluó, mediante cromatografía de gases con detector selectivo de masas GC-MS/SIM, la naturaleza química del biopolímero, a partir de la biomasa generada en un ensayo de fermentación en cultivo sumergido, con medio mínimo de sales suplementado con glucosa como fuente de carbono. Cuatro cepas de los morfotipos bacteriales encontrados, presentaron potencial para producir PHAs, de los cuales dos fueron identificados como miembros de la especie Bacillus megaterium, uno como B. mycoides y el otro como Gordonia sp. El gen PhaC se detectó en los dos aislamientos de B. megaterium. El análisis cromatográfico permitió detectar al Polihidroxibutirato (PHB) como el principal componente de los PHAs presentes en B. megaterium, cuantificándose entre 63.8 mg/g y 95.3 mg/g de PHB en los ensayos de fermentación. Las bacterias aisladas tienen potencial en la producción de PHAs a partir de residuos agroindustriales, incluyendo el jugo de fique, lo que contribuiría a la reducción de su condición contaminante.
Polyhydroxyalkanoates (PHAs) are biodegradable biopolymers of bacterial origin with properties similar to conventional plastics. In this work, bacteria were isolated from soils contaminated with fique wastes in the municipality of Guarne (Antioquia) and their ability to produce PHAs was evaluated. Bacteria were stained with Nile blue and Nile red and the PhaC gene detected by PCR. Positive bacteria were identified by phylogenetic analysis of 16S rDNA and biochemical tests. The chemical nature of the biopolimers was determined by gas chromatography GC-MS/SIM using biomass produced in a submerged fermentation in a minimal media supplemented with glucose as sole carbon source. Four bacterial morphotypes identified as Bacillus megaterium (2), B. mycoides (1) and Gordonia sp. (1) showed potential to produce PHAs. However, the PhaC gene was detected in B. megaterium. Chromatographic analysis showed polyhydroxybutirate (PHB) to be the main component in the PHAs produced by B. megaterium with levels between 63.8 mg/g and 95.3 mg/g in the fermentation test. The isolated bacteria have potential to produce PHAs, generating added value to the Agro-industrial waste, as in the fique industry, and reducing its contamination impact.
Subject(s)
Bacteria , Polyhydroxyalkanoates , Biopolymers , Plastics , SoilABSTRACT
La cepa Pseudomonas fluorescens IBUN S1602 conforma el grupo de aislamientos provenientes de suelos colombianos de caña de azúcar, que acumula polihidrioxialcanoato (PHA), fue seleccionada como promisoria para escalamiento comercial por tener afinidad por sustratos alternativos y económicos como el glicerol, aceites usados, suero de leche, entre otros. Dada la importancia de la enzima sintasa en la síntesis de los PHAs, en el presente trabajo se realizó el análisis molecular de los genes phaC1 y phaC2 que codifican las enzimas sintasas tipo II (PhaC1 y PhaC2). Para la obtención de los amplímeros requeridos en la secuenciación, se utilizó la técnica de PCR bajo condiciones estandarizadas para iniciadores diseñados reportados en las bases de datos. Se identificaron dos fragmentos de 1680 pb y 1683 pb correspondientes a phaC1 y phaC2. El análisis comparativo de las secuencias proteicas resultantes de estos genes demuestra que la sintasa IBUN S1602 contiene la región α/β hidrolasa y 8 residuos de aminoácidos conservados, que son características de las sintasas examinadas a nivel mundial. Se analizó la estructura enzimática a nivel primario y se predijo la secundaria. Se concluyó que las sintasas de la cepa Pseudomonas fluorescens IBUN S1602 presentan alta homología con las sintasas tipo II que se reportan para Pseudomonas. Los resultados obtenidos contribuyen al entendimiento básico de la biosíntesis de PHA, la cual permitirá, en un futuro, el aumento de la calidad de PHA debida a la modulación del nivel de sintasa que se exprese en un organismo recombinante, con el fin de variar el peso molecular del biopolímero, propiedad esencial en el estudio de aplicaciones industriales.
The strain Pseudomonas fluorescens IBUN S1602 forms the group of isolates from colombian sugarcane soil´s, which accumulates polyhydroxyalkanoate biopolymer (PHA) and was selected as promising for commercial scale by having affinity for economic and alternative substrates such as glycerol, oils, whey, among others. Given the importance of the synthase enzyme in the synthesis of PHAs, was realized the molecular analysis of genes phaC1 and phaC2 which encode type II synthases (PhaC1 y PhaC2). To obtain the amplimers required in the sequencing, was used the PCR technique under standardized conditions for primers designed based on the updated review in databases. Were identified two fragments of 1680 bp and 1683 bp for phaC1 and phaC2. Comparative analysis of the resulting protein sequences of these genes shows that the IBUN S1602 synthases containing the region α/β hydrolase and 8 conserved amino acid residues that are characteristic of synthases examined worldwide. Enzyme structure was analyzed at the primary level and was predicted the secondary. It is concluded that synthase strain Pseudomonas fluorescens IBUN S1602 has high homology with type II synthases that are reported for Pseudomonas. The results contribute to basic understanding of the biosynthesis of PHA, and will allow in the future, increasing the quality of PHA due to modulation of the level of synthase is expressed in a recombinant organism, in order to vary the weight molecular biopolymer, an essential property in the study of industrial applications.