Tesis por compendio / [ES] La producción y consumo de plásticos derivados de petróleo ha crecido exponencialmente en las últimas décadas, impactando en la naturaleza y los seres vivos. Los envases alimentarios son considerados la principal fuente de contaminación por plásticos. Por ello, el estudio y desarrollo de nuevos materiales derivados de recursos renovables y biodegradables ha emergido como un nuevo campo de gran interés. La presente tesis doctoral se enfocó en el desarrollo y caracterización de biopolímeros de polihidroxialcanoato (PHA) derivados de subproductos industriales y de la fracción orgánica de aguas residuales municipales, los residuos biológicos municipales, sintetizados por cultivos microbianos mixtos y producidos mediante las tecnologías de electroestirado y mezclado en fundido. Los materiales resultantes fueron desarrollados para obtener monocapas y multicapas activas y de alta barrera a oxígeno para su uso en envases alimentarios basados en la Bioeconomía Circular. Para lograr los objetivos, esta tesis doctoral se ha dividido en tres bloques según la tecnología utilizada en la obtención de los materiales. El primer bloque consistió en la extracción de los PHAs derivados de residuos agro-industriales para su óptima utilización en los procesos de producción. Posteriormente, se realizó el procesado de los PHAs mediante la técnica de electroestirado, por la cual se obtuvieron fibras poliméricas que fueron tratadas térmicamente para formar films continuos y homogéneos. Estas monocapas presentaron buenas propiedades térmicas y mecánicas, así como alta barrera tanto a vapores como a gases. Además, las fibras fueron funcionalizadas con compuestos orgánicos presentes en aceites esenciales para proporcionarles una función antimicrobiana activa contra microorganismos trasmitidos por los alimentos. Por otro lado, se realizó el electroestirado de copolímeros de etileno-alcohol vinílico, un polímero sintético que se biodegrada en condiciones específicas y que posee alta barrera a oxígeno. Además, nanocristales de celulosa fueron añadidos al EVOH, para crear monocapas híbridas de alta barrera más sostenibles. En el segundo bloque, los materiales se procesaron mediante la técnica de mezclado en fundido. Para ello, los PHAs derivados de biomasa del primer bloque se mezclaron con PHAs comerciales, así como con cargas celulósicas para formar "compuestos verdes", en el que todos los materiales estaban basados en recursos renovables y biodegradables. Las mezclas mostraron buena miscibilidad y propiedades ópticas, una flexibilidad mejorada, así como propiedades de barrera similares a las del material de biopoliéster puro. Finalmente, en el tercer bloque, se produjeron sistemas multicapas utilizando mezclas de PHA desarrolladas ad-hoc, y materiales monocapa de PHA electroestirado del primer bloque. Estas estructuras multicapas se basaron en las propiedades adhesivas que poseen las fibras electroestiradas tras aplicarles el tratamiento térmico y en el uso de los revestimientos de CNCs como capas intermedias de barrera a oxígeno. Así, los sistemas multicapas desarrollados fueron totalmente compostables, con alta barrera a oxígeno, siendo potenciales candidatos para sustituir a los actuales envases alimentarios basados en materiales no renovables provenientes del petróleo. Por lo tanto, los materiales aquí desarrollados son tanto bioadhesivos muy prometedores que muestran propiedades antimicrobianas y de alta barrera, como capas exteriores con fines estructurales o para uso como films finos. Así, por laminación, estos materiales pueden dar lugar a films multicapas autoadhesivos, empleados tanto en envases rígidos, semirrígidos o flexibles. Estas estructuras son sostenibles y respetuosas con el medio ambiente y además son biodegradables mediante compostaje y, en algún caso, biodegradables en el medio ambiente. Asimismo, son potencialmente capaces de proporcionar una calidad y seguridad alimentaria comparables a las derivadas de fuentes petroquímicas. / [CA] La producció i el consum de plàstics derivats de petroli ha crescut exponencialment en les últimes dècades, impactant en la naturalesa i els éssers vius. Els envasos alimentaris són considerats la principal font de contaminació per plàstics. Per això, l'estudi i el desenvolupament de nous materials derivats de recursos renovables i biodegradables ha emergit com un nou camp de gran interès. Aquesta tesi doctoral es va enfocar en el desenvolupament i la caracterització de biopolímers de polihidroxialcanoat (PHA) derivats de subproductes industrials i de la fracció orgànica d'aigües residuals municipals, els residus biològics municipals, sintetitzats per cultius microbians mixtos i produïts mitjançant les tecnologies d'electroestirat i barrejat en fosa. Els materials resultants van ser desenvolupats per obtenir monocapes i multicapes actives i d'alta barrera a oxigen per utilitzar-los en envasos alimentaris basats en la Bioeconomia Circular. Per assolir els objectius, aquesta tesi doctoral s'ha dividit en tres blocs segons la tecnologia utilitzada per obtenir els materials. El primer bloc va consistir en l'extracció dels PHA derivats de residus agroindustrials per a la seva òptima utilització en els processos de producció. Posteriorment, es va realitzar el processament dels PHA mitjançant la tècnica d'electroestirat, per la qual es van obtenir fibres polimèriques que van ser tractades tèrmicament per formar films continus i homogenis. Aquestes monocapes van presentar bones propietats tèrmiques i mecàniques, així com alta barrera tant a vapors com a gasos. A més, les fibres van ser funcionalitzades amb compostos orgànics presents en olis essencials per proporcionar-los una funció antimicrobiana activa contra microorganismes transmesos pels aliments. D'altra banda, es va realitzar l'electroestirat de copolímers d'etilè-alcohol vinílic, un polímer sintètic que es biodegrada en condicions específiques i que té alta barrera a oxigen. A més, nanocristalls de cel·lulosa van ser afegits a l'EVOH, per crear monocapes híbrides d'alta barrera més sostenibles. Al segon bloc, els materials es van processar mitjançant la tècnica de barrejat en fosa. Per això, els PHAs derivats de biomassa del primer bloc es van barrejar amb PHAs comercials, així com amb càrregues cel·lulòsiques per formar "compostos verds", en què tots els materials estaven basats en recursos renovables i biodegradables. Les barreges van mostrar bona miscibilitat i propietats òptiques, una flexibilitat millorada, així com propietats de barrera similars a les del material de biopolièster pur. Finalment, al tercer bloc, es van produir sistemes multicapes utilitzant barreges de PHA desenvolupades ad-hoc, i materials monocapa de PHA electroestirat del primer bloc. Aquestes estructures multicapes es van basar en les propietats adhesives que tenen les fibres electroestirades després d'aplicar-los el tractament tèrmic i en l'ús dels revestiments de CNC com a capes intermèdies de barrera a oxigen. Així, els sistemes multicapes desenvolupats van ser totalment compostables, amb alta barrera a oxigen, sent potencials candidats per substituir els actuals envasos alimentaris basats en materials no renovables provinents del petroli. Per tant, els materials aquí desenvolupats són tant bioadhesius molt prometedors que mostren propietats antimicrobianes i d'alta barrera, com a capes exteriors amb fins estructurals o per a ús com a films fins. Així, per laminació, aquests materials poden donar lloc a films multicapes autoadhesius, emprats tant en envasos rígids, semirígids o flexibles. Aquestes estructures són sostenibles i respectuoses amb el medi ambient ia més són biodegradables mitjançant compostatge i, en algun cas, biodegradables al medi ambient. Així mateix, són potencialment capaços de proporcionar una qualitat i seguretat alimentària comparables a les derivades de fonts petroquímiques. / [EN] The production and consumption of petroleum derived plastics that are not biodegradable has grown exponentially in recent decades, with the consequent impact on nature and organisms. The food packaging sector is today considered the main source of plastic contamination. Therefore, the study and development of new materials derived from renewable and biodegradable resources has emerged as a new field of great scientific, social, economic and political interest. The current PhD thesis focused on the development and characterization of polyhydroxyalkanoate (PHA) biopolymers derived from agro-industrial by-products and from the organic fraction of municipal wastewater, the municipal biowaste, synthesized by mixed microbial cultures and produced by electrospinning and melt compounding technologies. The resultant materials were particularly developed to obtain high-oxygen-barrier active monolayers and multilayers for use in Circular Bioeconomy-based food packaging. In order to achieve the objectives, this PhD thesis has been divided into three blocks according to the technology used to obtain the materials. The first block consisted of the extraction of PHAs derived from agro-industrial waste for their optimal use in production processes. After this, the PHAs were then processed using the electrospinning technique, whereby polymeric fibers were obtained and thermally post-treated by an annealing process to form continuous and homogeneous films, also known as "biopapers". These monolayers showed good thermal and mechanical properties, as well as a high barrier to both vapors and gases. In addition, the fibers were functionalized with eugenol, an organic compound present in essential oils, to provide them with active antimicrobial function against foodborne microorganisms. On the other hand, the electrospinning of poly(ethylene-co-vinyl alcohol) copolymers, a synthetic polymer that is claimed to biodegrade under specific conditions and with high oxygen barrier, was performed. Cellulose nanocrystals were added to EVOH, to create high barrier more sustainable hybrid monolayers. In the second block, the materials were processed using the melt compounding technique. For this purpose, the biomass derived PHAs extracted in the first block were blended with commercial PHAs as well as with cellulosic fillers, in this case rice husk flour, in order to form "green composites", where all the materials were based on renewable and biodegradable resources. After film formation by hot pressing, the blends showed excellent miscibility and optical properties, improved flexibility, as well as barrier properties similar to the neat biopolyester material. Finally, in the third block, multilayer systems were produced using ad-hoc developed PHA blends, and PHA electrospun monolayer materials developed in the first block. They were based on the adhesive properties of the electrospun fibers after thermal treatment, which allowed the elimination of synthetic adhesive substances normally used in the industry, and on the use of the CNCs coatings as oxygen barrier interlayers. Thus, the multilayer systems developed were fully compostable, with high oxygen barrier, being potential candidates to replace current food packaging based on non-renewable petroleum-based materials. Therefore, the materials developed herein are very promising bioadhesives showing antimicrobial and high barrier properties, as well as outer layers for structural or thin film purposes. Thus, by lamination, these materials can result in self-standing multilayer films, which can be used in rigid or semirigid packaging as well as in flexible packaging. They are sustainable and environmentally friendly, as they are made from renewable sources or waste, and are biodegradable by composting, and, in some case, even biodegradable in the environment. Furthermore, they are potentially capable of providing comparable quality and food safety to those currently marketed from petrochemical sources. / Meléndez Rodríguez, B. (2022). Development and Characterization of Monolayers and Multilayers Based on Biodegradable Materials Derived from Waste and By-products of Interest in Food Packaging [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/184651 / TESIS / Compendio

L’accumulation de biopolymère de réserve (PolyHydroxyAlcanoates ou PHA) par la souche Cupriavidus necator, à partir de substrats de type acides gras volatils (acide butyrique, acide propionique et acide acétique) a été étudiée. Elle est induite par une limitation phosphore. Les performances atteintes lors des cultures se situent parmi les meilleures de la littérature pour ce type de substrat : jusqu’à 66 g.L-1 de biomasse totale avec un pourcentage d’accumulation massique de 88% en PHB –PolyHydroxyButyrate- ou en PHB-co-HV -PolyHydroxyButyrate-co-HydroxyValerate- comportant jusqu’à 52% de motifs d’HV.Pour chaque source carbonée, une caractérisation cinétique et stœchiométrique de la souche a été réalisée en l’absence d’effets inhibiteurs dus aux substrats acides grâce à des cultures de type Fed-Batch avec des apports non limitants et non inhibiteurs en carbone. Il a été dégagé :- un taux de croissance maximal de la souche de 0,33 h-1 pour les trois acides étudiés- une relation entre vitesse spécifique de production de PHA et taux de croissance fixée par la disponibilité et les flux de production de NADPH2 avec un découplage inverse pour les taux de croissance supérieurs à 0,05 h-1 et un couplage partiel pour les taux de croissance inférieurs- un optimum de 0,35 Cmole.Cmole-1.h-1, associé à un taux de croissance de l’ordre de 0,05 h-1.- une amélioration de la production de PHB en termes de vitesses spécifiques mais également en termes de rendements si une faible croissance résiduelle est maintenueLa réponse de la souche à un excès de substrat acide a été caractérisée via l’étude de régimes transitoires induits par des pulses sur des cultures continues préalablement stabilisées en régime permanent. Il a été montré qu’en excès de phosphore, face à un brusque excès de substrat, la souche est incapable d’adapter rapidement son taux de croissance. L’excès est donc dirigé vers la production de PHA dont les voies sont plus rapidement mobilisables. En conditions limitantes de phosphore, le substrat excédentaire est utilisé pour la production de PHA. L’inhibition par les acides se traduit par une diminution des capacités de biosynthèse de la biomasse et des PHA entrainant une réduction de l’assimilation du carbone puis une diminution des rendements de conversion. D’autre part la sensibilité d’un système continu à un excès de substrat dépend du point de fonctionnement choisi : plus il est optimal en termes de vitesse, moins le système est robuste. L’acide propionique est très inhibiteur comparé aux autres acides étudiés (dès 3-4 mM contre 30-40 mM). Il n’agit pas simplement via une accumulation excessive dans le cytoplasme mais il exerce également une inhibition spécifique des voies métaboliques.Un antagonisme entre les substrats (acide acétique et butyrique) a été constaté et expliqué grâce à une analyse des flux métaboliques. L’acide acétique est assimilé préférentiellement pour produire la biomasse, l’énergie et les cofacteurs nécessaires à la production de PHA, alors que l’acide butyrique est utilisé pour la synthèse de PHB. La proportion maximale d’acide acétique admise dans l’alimentation en fonction des conditions fixées en régime permanent est calculée et peut être limitée à 40% du carbone.Enfin il a été déterminé que si une croissance résiduelle est assurée grâce à un apport en phosphore, le pourcentage maximal d’HV dans le polymère dépend du taux d’acide propionique dans l’alimentation et ne peux dépasser 33 ± 5% sur acide propionique pur. Par contre, si aucune croissance résiduelle n’est assurée, il est possible de convertir l’acide propionique en motifs d’HV uniquement / Reserve Biopolymer (PolyHydroxyAlkanoates or PHA) accumulation by the strain Cupriavidus necator, from Volatile Fatty Acids (VFA, like butyric acid, propionic acid and acetic acid) was investigated. This production is induced by a phosphorus limitation. For this type of substrates, performances reached during cultures are among the best listed in the literature: up to 66 g.L-1 of total biomass with 88% (w/w) of PHB –PolyHydroxyButyrate- or PHB-co-HV -PolyHydroxyButyrate-co-HydroxyValerate- with a HV content up to 52 Mole%.For each carbon source, kinetic and stoechiometric characterization has been carried out thanks to Fed-Batch cultures with non-limiting and non-inhibitory carbon feed. It has been established:- a maximal growth rate of 0,33 h-1 for the three acid investigated- a relationship between specific PHA production rate and growth rate which is set by the availability and production flux of NADPH2. For growth rate above 0,05 h-1, there is an inverse coupling. For growth rate under 0,05 h-1, there is a partial coupling.- an optimum of 0,35 Cmole.Cmole-1.h-1 is associated with a growth rate of 0,05 h-1.- if a low residual growth rate is maintained, an improvement of PHB production is recorded in terms of specific production rate and yieldsThe response of the strain to an excess of acid substrate was characterized through the investigation of transient state induced by pulsed addition of substrate during continuous cultures stabilized in steady state. It was shown that in excess of phosphorus, when there is a substrate excess, the strain is unable to quickly adapt its growth rate, so the excess is directed to PHA production whose ways seem to be more easily mobilized. Under phosphorus limitation, an excess of substrate is used for PHA production. Acid inhibition results in a decrease in biomass and PHA production capacity which leads to a decrease in carbon assimilation and conversion yields. The sensitivity of a continuous system to an excess of substrate depends on the chosen operating point: the more it is optimal in terms of specific production rate, the less the system is robust. Propionic acid is highly inhibitory compared to the other acids studied (from 3-4 mM versus 30-40 mM). It does not act only via an excessive accumulation in the cytoplasm but also exerts a specific inhibition of metabolic pathways.An antagonism between substrates (acetic and butyric acid) has been established and explained thanks to the Metabolic Flux Analysis. Acetic acid is preferentially used to produce biomass, energy and cofactors for PHA synthesis, whereas butyric acid is used to product PHB. According to the conditions set during steady state, maximal content of acetic acid admitted in the feed can be calculated. It can be limited to 40% of the carbon in the feed.Finally if a growth rate is maintained thanks to a phosphorus supply, the maximal HV content in polymer is function of propionic acid in the feed and cannot exceed 33 ± 5 Mole% on pure propionic acid. Conversely, if there is no residual growth, a total conversion of propionic acid into HV is allowed

O objetivo deste trabalho foi produzir poli-3-hidroxibutirato (P3HB) e poli-3-hidroxibutirato-co-3-hidroxivalerato (PHB-co-3HV), polímeros biodegradáveis, utilizando hidrolisado hemicelulósico, rico em xilose, de bagaço de cana-de-açúcar. O estudo dos fluxos metabólicos de xilose in silico indicou que, através do redirecionamento do metabolismo, é possível aumentar o rendimento P3HB a partir de xilose de 0.25 g g-1 para 0.40 g g-1. Obtiveram-se mutantes no sistema repressão catabólica nos quais se verificaram consumo simultâneo de carboidratos e redução do tempo de consumo dos açúcares. Porém, diferenças de fluxos de carbono resultaram em menores valores de crescimento e produção de PH3B em relação às linhagens parentais. Um programa de bioprospecção destacou Burkholderia sp. F24, em experimentos em biorreator obteve-se 25.04 g l-1 de biomassa, 49.31% de acúmulo de P3HB na massa seca celular, alcançando uma produtividade de 0.28 g l-1 h-1. Além disso, foi possível controlar a fração molar de 3HV na síntese PHB-3HV em F24 utilizando xilose e ácido levulínico. / The aim of this thesis is to produce poly3-hydroxybutyrate (P3HB) and poli-3-hidroxibutirate-co-3-hydroxyvalerate (PHB-co-3HV), biodegradable polymers, using hemicellulosic hydrolysate, rich in xylose, from sugarcane bagasse. Metabolic flux analysis in silico of xylose metabolism indicated that, though metabolism redirection is possible to increase P3HB yield from 0.25 g g-1 to 0.40 g g-1. It was observed simultaneous consumption of sugars and reduction of time necessary to exhaust of all sugars in the media culture in mutants with catabolite repression partially abolished. However, differences in carbon flux resulted in lower growth and P3HB production in comparison to the parental strain. A bioprospecting program selected Burkholderia sp. F24, in experiments in bioreactor it reached 25.04 g l-1, 49.31% of P3HB accumulation of the dry cell mass and 0.28 g l-1 h-1 of productivity. Moreover, it was possible to modulate to molar fraction of 3HV in PHB-co-3HV biosyntheses with Burkholderia sp. F24 using xylose and levulinic acid.

Os polihidroxialcanoatos (PHAs) são poliésteres acumulados por microrganismos como material de reserva. O conhecimento das vias bioquímicas e enzimas envolvidas na biossíntese e degradação dos PHAs é uma importante ferramenta para auxiliar na produção industrial. A linhagem Burkholderia cepacia IPT64 é capaz de acumular uma blenda composta de P(3HB) e P(3H4PE) a partir de sacarose. Este trabalho está focado em duas das principais enzimas envolvidas na biossíntese de PHAs: a b-cetotiolase (phaA) e a PHA sintase (phaC). A primeira está associada à especificidade pelo substrato, e a segunda é considerada a enzima chave na síntese de PHAs. Neste trabalho a linhagem mutante phaC foi avaliada quanto à atividade enzimática de PHB sintase, que se constatou ter sido perdida. A presença de mais de uma tiolase no genoma de B. cepacia foi detectada. A inativação do gene phaABc identificado anteriormente, bloqueou totalmente a síntese de P(3HB), e não promoveu o aumento da quantidade total de polímero. Este resultado indica que a tiolase identificada é responsável direta do acúmulo de P(3HB). Outra indicação é que não há uma competição das vias de síntese dos dois polímeros P(3HB) e P(3H4PE), já que não houve alteração na quantidade de P(3H4PE) acumulado, mesmo quando P(3HB) deixou de ser acumulado. / The polyhydroxyalkanoates (PHAs) are polyesters accumulated by microorganisms as storage compounds. Knowing the biochemistry pathway and enzymes involved in the biosynthesis and degradation of PHAs is an important tool to help industrial production. The Burkholderia cepacia IPT64 strain is able to accumulate a blend of P(3HB) and P(3H4PE) from sucrose. The focus of this work is on the two main enzymes involved in PHA biosynthesis: the b-ketothiolase (phaA) and the PHA synthase (phaC). The first one is associated with substrate specificity, and the second one is considered the key enzyme in PHA synthesis. In this work a mutant strain phaC was evaluated on its PHB synthase enzymatic activity, that was discovered to have been lost. The presence of other thiolases in the B. cepacia genome was detected. The inactivation of phaABc gene identified previously, blocked totally the P(3HB) synthesis, and didnt increase the polymer content. This result indicates that the identified thiolase is directly responsible for P(3HB) accumulation. Another indication is that the synthesis pathways of the two polymers, P(3HB) and P(3H4PE), dont compete with each other, because the content of P(3H4PE) was not altered, even when the P(3HB) was not accumulated.

O objetivo deste trabalho foi produzir poli-3-hidroxibutirato (P3HB) e poli-3-hidroxibutirato-co-3-hidroxivalerato (PHB-co-3HV), polímeros biodegradáveis, utilizando hidrolisado hemicelulósico, rico em xilose, de bagaço de cana-de-açúcar. O estudo dos fluxos metabólicos de xilose in silico indicou que, através do redirecionamento do metabolismo, é possível aumentar o rendimento P3HB a partir de xilose de 0.25 g g-1 para 0.40 g g-1. Obtiveram-se mutantes no sistema repressão catabólica nos quais se verificaram consumo simultâneo de carboidratos e redução do tempo de consumo dos açúcares. Porém, diferenças de fluxos de carbono resultaram em menores valores de crescimento e produção de PH3B em relação às linhagens parentais. Um programa de bioprospecção destacou Burkholderia sp. F24, em experimentos em biorreator obteve-se 25.04 g l-1 de biomassa, 49.31% de acúmulo de P3HB na massa seca celular, alcançando uma produtividade de 0.28 g l-1 h-1. Além disso, foi possível controlar a fração molar de 3HV na síntese PHB-3HV em F24 utilizando xilose e ácido levulínico. / The aim of this thesis is to produce poly3-hydroxybutyrate (P3HB) and poli-3-hidroxibutirate-co-3-hydroxyvalerate (PHB-co-3HV), biodegradable polymers, using hemicellulosic hydrolysate, rich in xylose, from sugarcane bagasse. Metabolic flux analysis in silico of xylose metabolism indicated that, though metabolism redirection is possible to increase P3HB yield from 0.25 g g-1 to 0.40 g g-1. It was observed simultaneous consumption of sugars and reduction of time necessary to exhaust of all sugars in the media culture in mutants with catabolite repression partially abolished. However, differences in carbon flux resulted in lower growth and P3HB production in comparison to the parental strain. A bioprospecting program selected Burkholderia sp. F24, in experiments in bioreactor it reached 25.04 g l-1, 49.31% of P3HB accumulation of the dry cell mass and 0.28 g l-1 h-1 of productivity. Moreover, it was possible to modulate to molar fraction of 3HV in PHB-co-3HV biosyntheses with Burkholderia sp. F24 using xylose and levulinic acid.

Os polihidroxialcanoatos (PHAs) são poliésteres acumulados por microrganismos como material de reserva. O conhecimento das vias bioquímicas e enzimas envolvidas na biossíntese e degradação dos PHAs é uma importante ferramenta para auxiliar na produção industrial. A linhagem Burkholderia cepacia IPT64 é capaz de acumular uma blenda composta de P(3HB) e P(3H4PE) a partir de sacarose. Este trabalho está focado em duas das principais enzimas envolvidas na biossíntese de PHAs: a b-cetotiolase (phaA) e a PHA sintase (phaC). A primeira está associada à especificidade pelo substrato, e a segunda é considerada a enzima chave na síntese de PHAs. Neste trabalho a linhagem mutante phaC foi avaliada quanto à atividade enzimática de PHB sintase, que se constatou ter sido perdida. A presença de mais de uma tiolase no genoma de B. cepacia foi detectada. A inativação do gene phaABc identificado anteriormente, bloqueou totalmente a síntese de P(3HB), e não promoveu o aumento da quantidade total de polímero. Este resultado indica que a tiolase identificada é responsável direta do acúmulo de P(3HB). Outra indicação é que não há uma competição das vias de síntese dos dois polímeros P(3HB) e P(3H4PE), já que não houve alteração na quantidade de P(3H4PE) acumulado, mesmo quando P(3HB) deixou de ser acumulado. / The polyhydroxyalkanoates (PHAs) are polyesters accumulated by microorganisms as storage compounds. Knowing the biochemistry pathway and enzymes involved in the biosynthesis and degradation of PHAs is an important tool to help industrial production. The Burkholderia cepacia IPT64 strain is able to accumulate a blend of P(3HB) and P(3H4PE) from sucrose. The focus of this work is on the two main enzymes involved in PHA biosynthesis: the b-ketothiolase (phaA) and the PHA synthase (phaC). The first one is associated with substrate specificity, and the second one is considered the key enzyme in PHA synthesis. In this work a mutant strain phaC was evaluated on its PHB synthase enzymatic activity, that was discovered to have been lost. The presence of other thiolases in the B. cepacia genome was detected. The inactivation of phaABc gene identified previously, blocked totally the P(3HB) synthesis, and didnt increase the polymer content. This result indicates that the identified thiolase is directly responsible for P(3HB) accumulation. Another indication is that the synthesis pathways of the two polymers, P(3HB) and P(3H4PE), dont compete with each other, because the content of P(3H4PE) was not altered, even when the P(3HB) was not accumulated.

The diploma thesis is focused on the study of the mechanism of plasticization of polyhydroxyalkanoates (PHA) in vivo, focusing mainly on methods of isolation native PHA granules and physical and chemical methods of initiation their phase transitions. The literature search prepared in this work deals with this microbial polyester and further focuses on individual methods of isolating PHA from bacterial cells. The main task of the experimental work was to optimize the isolation process of native PHA granules, as well as to design and test processes that initiate the PHA crystallization in isolated granules, as well as analytical procedures to correctly detect this phase transition. Isolation of PHA granules from Cupriavidus necator was performed by enzymes, centrifugation several times and sonication of the cells. Fourier transform infrared spectroscopy (FTIR) and an enzymatic method in which amorphous PHA is selectively degraded by PHA-depolymerase with turbidimetric detection of its loss in dispersion was used to detect PHA crystallization. Techniques based on fluorescence staining of granules (fluorescence spectroscopy and flow cytometry) were used in a more detailed study of the mechanism of PHA plasticization in granules. The results of the analyzes confirmed, among other things, that the optimized procedure makes it possible to isolate granules in the amorphous state, which remain amorphous even after drying and are comparable to native granules in their basic physicochemical properties.

This diploma thesis deals with application of evolutionary engineering on PHA producing bacterial strains. Two bacterial strains, Cupriavidus necator H16 and Halomonas halophila, were chosen for the evolutionary experiments. Copper cations (Cu2+) and sodium chloride (NaCl) were chosen as the selective pressure for C. necator H16; acetic acid (AA) and levulinic acid (LA) for Halomonas halophila. The adapted strains were during long-time evolutionary experiments characterized by GC-FID and SEC-MALS. The growth of the adapted strains was studied by the mean of optical density measurement. The amount of viable cells was determined by spectral FC after their expositon to selected stress factors. Specific enzyme activities of enzymes involved in citrate and glyoxalate cycle, enzymes generating NADPH, LA metabolism enzyme and PHA biosynthesis enzymes were determined. The adapted strains were compared with the wild-type of strains. The successfull adaptation of C. necator H16 adapted to Cu2+ was detected. Biomass and PHA production of both wild and adapted H. halophila strains cultivated in lignocellulosis waste were determined. It was found out that H. halophila adapted to the LA is capable of producing more PHA than the wild strain of this bacteria.

This thesis deals with the characterization of bacterial cells capable of polyhydroxyalkanoates (PHA) accumulation. The dissertation thesis is written in the form of a discussed published publications which are attached to the thesis as appendixes. The work develops a study of the current topic of the protective functions of PHA and clarifies protective mechanisms against selected stressors. Firstly, we focused on the protective effects of PHA granules against UV radiation and osmotic stress, specifically hypotonic conditions. In the case of UV exposition, the cells protected themselves by scattering UV radiation on the intracellular granules protecting especially nucleoid. When exposed to osmotic stress, the amorphous state of PHA granules is very important since it is capable of stabilization of cell membranes under hypertonic stress, afterwards, bacterial cells can maintain their integrity during the subsequent hypotonic challenge. In general, the amorphous state of PHA granules is key to ensure the proper biological functions of PHA whether as storage or protective polymer. Therefore, in the next part of this work, we focused on the core of the stabilization mechanism that protects native PHA granules from crystallization and thus the intracellular polymer maintains in a thermodynamically unfavorable amorphous phase state. Based on experimental work, we applied selected stresses because we proposed a new model of stabilization of the amorphous state of PHA granules in vivo. It consists of two mechanisms, where small volumes of PHA granules reduce the rates of crystallization and at the same time the water present in the granules plays the role of a low molecular plasticizer. Due to the metabolic apparatus of bacterial cells, PHA are simultaneously synthesized and degraded which leads to an increment of intracellular concentration of monomers that also figure in the protective effect of PHA. In this context, we aimed at the description of the mechanism of cryoprotective effects of 3-hydroxybutyrate, the monomer of the most common of PHA, poly(3-hydroxybutyrate). Hence, we constructed an equilibrium and non-equilibrium phase diagram of the 3HB-water system to prove that 3HB is a very effective cryoprotectant. This fundamental understanding of the protective properties of PHA monomers could be also used in the food industry or cryopreservation of biological samples.

Tesis por compendio / [ES] El envasado activo es una de las tecnologías emergentes más relevantes de la industria alimentaria. Su objetivo es interactuar con el espacio de cabeza del envase para controlar las reacciones enzimáticas, químicas, físicas y microbiológicas que deterioran los alimentos por medio de la absorción o liberación. La actual tesis doctoral trata originalmente del desarrollo y la caracterización de estructuras de envasado de alimentos activas y biodegradables mono y multicapa basadas en materiales de polihidroxialcanoatos (PHA) electroestirados derivados de estrategias de bioeconomía circular. Con el fin de dotar con propiedades activas los materiales de envasado, se incorporaron a los PHA aceites esenciales, extractos naturales, nanopartículas metálicas o combinaciones de los mismos mediante electrospinning de soluciones. Las fibras resultantes de PHA por electrospinning se recocieron para obtener monocapas continuas que, posteriormente, se combinaron con películas de polímeros biodegradables fundidas, sopladas o fundidas con disolventes y/o con revestimientos de barrera de nanocristales de celulosa bacteriana (CNC) para desarrollar novedosos sistemas multicapa con propiedades antimicrobianas y de barrera. Estos sistemas multicapas basados en PHA presentaron un buen rendimiento térmico y mecánico, así como altas propiedades de barrera a los vapores y gases. Las películas activas también mostraron mejores propiedades antioxidantes y una alta actividad antimicrobiana contra las bacterias transmitidas por los alimentos tanto en sistemas abiertos como, lo que es más importante, en sistemas cerrados, que pueden imitar las condiciones de envasado en casos reales. Por lo tanto, los materiales y prototipos desarrollados en este trabajo pueden ser muy prometedores como materiales de envasado, para constituir bandejas, flow packs y tapas, siendo completamente renovables y también biodegradables, con una potencial capacidad de aumentar tanto la calidad, como la seguridad de los productos alimenticios en el nuevo contexto de la Bioeconomía Circular. / [CA] L'envasament actiu és una de les tecnologies emergents més rellevants de la indústria alimentària. El seu objectiu és interactuar amb l'espai de cap de l'envàs per controlar les reaccions enzimàtiques, químiques, físiques i microbiològiques que deterioren els aliments per mitjà de l'absorció o alliberament. L'actual tesi doctoral tracta originalment de el desenvolupament i la caracterització d'estructures d'envasat d'aliments actives i biodegradables mono i multicapa basades en materials de polihidroxialcanoatos (PHA) electroestirados derivats d'estratègies de bioeconomia circular. Per tal de dotar amb propietats actives dels materials d'envasat, es van incorporar als PHA olis essencials, extractes naturals, nanopartícules metàl·liques o combinacions dels mateixos mitjançant electrospinning de solucions. Les fibres resultants de PHA per electrospinning es recocieron per obtenir monocapes contínues que, posteriorment, es van combinar amb pel·lícules de polímers biodegradables foses, bufades o foses amb dissolvents i / o amb revestiments de barrera de nanocristalls de cel·lulosa bacteriana (CNC) per desenvolupar nous sistemes multicapa amb propietats antimicrobianes i de barrera. Aquests sistemes multicapes basats en PHA van presentar un bon rendiment tèrmic i mecànic, així com altes propietats de barrera als vapors i gasos. Les pel·lícules actives també van mostrar millors propietats antioxidants i una alta activitat antimicrobiana contra bacteris transmeses pels aliments tant en sistemes oberts com, el que és més important, en sistemes tancats, que poden imitar les condicions d'envasament en casos reals. Per tant, els materials i prototips desenvolupats poden ser molt prometedors com materials d'envasat, per constituir safates, flow packs i tapes, sent completament renovables i també biodegradables, amb la capacitat potencial final d'augmentar tant la qualitat, com la seguretat de els productes alimentaris en el nou context de l'Bioeconomia Circular. / [EN] Active packaging is one of the most relevant emerging technologies in the food industry. It aims to interact with the packaging headspace to control the enzymatic, chemical, physical, and microbiological reactions that deteriorate food through scavenging or releasing means. The current PhD thesis originally deals with the development and characterization of mono and multilayer active and biodegradable food packaging structures based on electrospun polyhydroxyalkanoates (PHA) materials derived from circular bioeconomy strategies. In order to provide the packaging materials with active properties, essential oils, natural extracts, metallic nanoparticles or combinations thereof were incorporated into PHA by solution electrospinning. The resultant electrospun PHA mats were annealed to obtain continuous monolayers that were, thereafter, combined with cast-extruded, blown or solvent-casted biodegradable polymer films and/or barrier coatings of bacterial cellulose nanocrystals (CNCs) to develop novel multilayer systems with antimicrobial and barrier properties. These PHA-based multilayers systems presented good thermal and mechanical performance as well as high barrier properties to vapors and gases. The active films also showed improved antioxidant properties and high antimicrobial activity against food-borne bacteria in both open and, more importantly, closed systems, which can mimic real case use packaging conditions. Therefore, the here-developed materials and prototypes can be very promising as packaging materials, to constitute trays, flow packs and lids, being completely renewable and also biodegradable, with the final potential capacity to increase both quality and safety of food products in the new Circular Bioeconomy context. / Al programa Santiago Grisolía de la Generalitat Valenciana (0001426013N810001A201) por concederme la beca Predoctoral. Al proyecto EU H2020 YPACK “High Performance Polyhydroxyalkanoates Based Packaging to Minimise Food Waste” (Grant agreement 773872) de la Comisión Europea. Al proyecto RTI2018-097249-B-C21 financiado por el Ministerio de Ciencia e Innovación de España. A la Unidad Asociada IATA-UJI en “Polymer Technology”. / Figueroa López, KJ. (2021). Biodegradable Mono and Multilayer Materials with Antimicrobial Capacity Based on Circular Bioeconomy of Application Interest in Food Packaging [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/168439 / TESIS / Compendio