RESUMEN
Naturally evolved enzymes, despite their astonishingly large variety and functional diversity, operate predominantly through thermochemical activation. Integrating prominent photocatalysis modes into proteins, such as triplet energy transfer, could create artificial photoenzymes that expand the scope of natural biocatalysis1-3. Here, we exploit genetically reprogrammed, chemically evolved photoenzymes embedded with a synthetic triplet photosensitizer that are capable of excited-state enantio-induction4-6. Structural optimization through four rounds of directed evolution afforded proficient variants for the enantioselective intramolecular [2+2]-photocycloaddition of indole derivatives with good substrate generality and excellent enantioselectivities (up to 99% enantiomeric excess). A crystal structure of the photoenzyme-substrate complex elucidated the non-covalent interactions that mediate the reaction stereochemistry. This study expands the energy transfer reactivity7-10 of artificial triplet photoenzymes in a supramolecular protein cavity and unlocks an integrated approach to valuable enantioselective photochemical synthesis that is not accessible with either the synthetic or the biological world alone.
Asunto(s)
Biocatálisis , Reacción de Cicloadición , Enzimas , Procesos Fotoquímicos , Biocatálisis/efectos de la radiación , Transferencia de Energía , Estereoisomerismo , Enzimas/genética , Enzimas/metabolismo , Enzimas/efectos de la radiación , Indoles/química , Especificidad por Sustrato , Cristalización , Evolución Molecular Dirigida/métodosRESUMEN
The ability to program new modes of catalysis into proteins would allow the development of enzyme families with functions beyond those found in nature. To this end, genetic code expansion methodology holds particular promise, as it allows the site-selective introduction of new functional elements into proteins as noncanonical amino acid side chains1-4. Here we exploit an expanded genetic code to develop a photoenzyme that operates by means of triplet energy transfer (EnT) catalysis, a versatile mode of reactivity in organic synthesis that is not accessible to biocatalysis at present5-12. Installation of a genetically encoded photosensitizer into the beta-propeller scaffold of DA_20_00 (ref. 13) converts a de novo Diels-Alderase into a photoenzyme for [2+2] cycloadditions (EnT1.0). Subsequent development and implementation of a platform for photoenzyme evolution afforded an efficient and enantioselective enzyme (EnT1.3, up to 99% enantiomeric excess (e.e.)) that can promote intramolecular and bimolecular cycloadditions, including transformations that have proved challenging to achieve selectively with small-molecule catalysts. EnT1.3 performs >300 turnovers and, in contrast to small-molecule photocatalysts, can operate effectively under aerobic conditions and at ambient temperatures. An X-ray crystal structure of an EnT1.3-product complex shows how multiple functional components work in synergy to promote efficient and selective photocatalysis. This study opens up a wealth of new excited-state chemistry in protein active sites and establishes the framework for developing a new generation of enantioselective photocatalysts.
Asunto(s)
Biocatálisis , Reacción de Cicloadición , Enzimas , Procesos Fotoquímicos , Aminoácidos/química , Aminoácidos/metabolismo , Reacción de Cicloadición/métodos , Estereoisomerismo , Biocatálisis/efectos de la radiación , Enzimas/química , Enzimas/genética , Enzimas/metabolismo , Enzimas/efectos de la radiación , Cristalografía por Rayos X , Dominio Catalítico , Código Genético , Diseño de FármacosRESUMEN
Bovine colostrum (BC) contains bioactive proteins, such as immunoglobulin G (IgG), lactoferrin (LF) and lactoperoxidase (LP). BC was subjected to low-temperature, long-time pasteurization (LTLT, 63 °C, 30 min) or high-temperature, short-time pasteurization (HTST, 72 °C, 15 s) and spray-drying (SD), with or without γ-irradiation (GI, â¼14 kGy) to remove microbial contamination. Relative to unpasteurized liquid BC, SD plus GI increased protein denaturation by 6 and 11%, respectively, increasing to 19 and 27% after LTLT and to 48% after HTST, with no further effects after GI (all P < 0.05). LTLT, without or with GI, resulted in 15 or 29% denaturation of IgG, compared with non-pasteurized BC, and 34 or 58% for HTST treatment (all P < 0.05, except LTLT without GI). For IgG, only GI, not SD or LTLT, increased denaturation (30-38%, P < 0.05) but HTST increased denaturation to 40%, with further increases after GI (60%, P < 0.05). LTLT and HTST reduced LP levels (56 and 81% respectively) and LTLT reduced LF levels (21%), especially together with GI (47%, P < 0.05). Denaturation of BSA, ß-LgA, ß-LgB and α-La were similar to IgG. Methionine, a protective amino acid against free oxygen radicals, was oxidised by LTLT + GI (P < 0.05) while LTLT and HTST had no effect. Many anti-inflammatory proteins, including serpin anti-proteinases were highly sensitive to HTST and GI but preserved after LTLT pasteurization. LTLT, followed by SD is an optimal processing technique preserving bioactive proteins when powdered BC is used as a diet supplement for sensitive patients.
Asunto(s)
Calostro/química , Desecación/métodos , Pasteurización/métodos , Proteínas , Animales , Bovinos , Frío , Enzimas/análisis , Enzimas/química , Enzimas/efectos de la radiación , Femenino , Calor , Inmunoglobulinas/análisis , Inmunoglobulinas/química , Inmunoglobulinas/efectos de la radiación , Desnaturalización Proteica , Proteínas/análisis , Proteínas/química , Proteínas/efectos de la radiación , Proteoma/análisis , Proteoma/química , Proteoma/efectos de la radiaciónRESUMEN
Ultraviolet photodissociation (UVPD) produces rich and informative fragmentation of intact protein ions, but in the case of high mass proteins (>30 kDa) the spectra are congested with overlapping isotope patterns of highly charged fragment ions. In the most congested regions, many fragments cannot be confidently identified even when high-resolution mass analyzers and modern deconvolution algorithms are used. Gas-phase ion-ion proton transfer reactions (PTR), which reduce the charge states of highly charged ions, can be used to alleviate this congestion and facilitate the identification of additional fragment ions when performed following UVPD. We have developed protocols for sequentially performing PTR on multiple populations of ions generated by UVPD in a way that can be tailored to balance the depth of characterization with speed and throughput. The improvements in sequence coverage and fragment identifications are demonstrated for four proteins ranging in size from 29 to 56 kDa. Sequence coverages up to 80% were achieved for carbonic anhydrase (29 kDa), 50% for aldolase (39 kDa), 46% for enolase (46 kDa), and 27% for glutamate dehydrogenase (56 kDa), and up to 74% sequence coverage was obtained for 25 kDa antibody drug conjugate subunits in online LC-MS experiments.
Asunto(s)
Enzimas/química , Inmunoconjugados/química , Protones , Secuencia de Aminoácidos , Animales , Bovinos , Cromatografía Liquida/métodos , Enzimas/efectos de la radiación , Inmunoconjugados/efectos de la radiación , Límite de Detección , Proteolisis/efectos de la radiación , Conejos , Saccharomyces cerevisiae/enzimología , Proteínas de Saccharomyces cerevisiae/química , Proteínas de Saccharomyces cerevisiae/efectos de la radiación , Espectrometría de Masas en Tándem/métodos , Rayos UltravioletaRESUMEN
The light-dependent metabolism of the white rot basidiomycete Cerrena unicolor FCL139 has already been demonstrated using transcriptomic and Biolog-based approaches. To further analyze the influence of light on C. unicolor wood degradation, we measured the activity of an array of CAZymes (carbohydrate-active enzymes) and enzymes involved in the redox system of fungal cells associated with lignolysis. Extra- and intracellular enzymatic extracts were obtained from solid-state ash sawdust C. unicolor cultures cultivated for 14 days under red, blue, green, or white light conditions, or in the dark. Light greatly influenced the synthesis of MnP, total cellulases, endo-1,4-ß-glucanase, endo-1,4-ß-xylanase, catalase, and superoxide dismutase. The production of MnP and catalase was evidently stimulated by white light. It is also worth noticing that blue light caused a gradual increase in the activity of total cellulases throughout the entire period of C. unicolor growth. Moreover, endo-1,4-ß-glucanase showed the highest activity on day 13 of fungus cultivation and the production of laccase and ß-glucosidase appeared to be the least influenced by light. However, the strongest activity of the endo-1,4-ß-xylanase was observed in the dark. It seemed that light not only influenced the regulation of the synthesis of the wood-degrading enzymes at different levels, but also acted indirectly by affecting production of enzymes managing harmful lignin by-products causing oxidative stress. The ability of the fungus to decompose woody plant material is clearly influenced by environmental factors.
Asunto(s)
Enzimas/biosíntesis , Polyporaceae/enzimología , Madera/química , Basidiomycota/enzimología , Enzimas/efectos de la radiación , Fermentación , Fraxinus , Proteínas Fúngicas/biosíntesis , Proteínas Fúngicas/efectos de la radiación , Luz , Lignina/metabolismo , Estrés OxidativoRESUMEN
Living organisms rely on simultaneous reactions catalysed by mutually compatible and selective enzymes to synthesize complex natural products and other metabolites. To combine the advantages of these biological systems with the reactivity of artificial chemical catalysts, chemists have devised sequential, concurrent, and cooperative chemoenzymatic reactions that combine enzymatic and artificial catalysts1-9. Cooperative chemoenzymatic reactions consist of interconnected processes that generate products in yields and selectivities that cannot be obtained when the two reactions are carried out sequentially with their respective substrates2,7. However, such reactions are difficult to develop because chemical and enzymatic catalysts generally operate in different media at different temperatures and can deactivate each other1-9. Owing to these constraints, the vast majority of cooperative chemoenzymatic processes that have been reported over the past 30 years can be divided into just two categories: chemoenzymatic dynamic kinetic resolutions of racemic alcohols and amines, and enzymatic reactions requiring the simultaneous regeneration of a cofactor2,4,5. New approaches to the development of chemoenzymatic reactions are needed to enable valuable chemical transformations beyond this scope. Here we report a class of cooperative chemoenzymatic reaction that combines photocatalysts that isomerize alkenes with ene-reductases that reduce carbon-carbon double bonds to generate valuable enantioenriched products. This method enables the stereoconvergent reduction of E/Z mixtures of alkenes or reduction of the unreactive stereoisomers of alkenes in yields and enantiomeric excesses that match those obtained from the reduction of the pure, more reactive isomers. The system affords a range of enantioenriched precursors to biologically active compounds. More generally, these results show that the compatibility between photocatalysts and enzymes enables chemoenzymatic processes beyond cofactor regeneration and provides a general strategy for converting stereoselective enzymatic reactions into stereoconvergent ones.
Asunto(s)
Biocatálisis/efectos de la radiación , Técnicas de Química Sintética/métodos , Enzimas/metabolismo , Enzimas/efectos de la radiación , Luz , Fotoquímica/métodos , Alcoholes/química , Alquenos/química , Aminas/química , Productos Biológicos/síntesis química , Productos Biológicos/química , Carbono/química , Cinética , EstereoisomerismoRESUMEN
In nature, a multitude of mechanisms have emerged for regulating biological processes and, specifically, protein activity. Light as a natural regulatory element is of outstanding interest for studying and modulating protein activity because it can be precisely applied with regard to a site of action, instant of time, or intensity. Naturally occurring photoresponsive proteins, predominantly those containing a light-oxygen-voltage (LOV) domain, have been characterized structurally and mechanistically and also conjugated to various proteins of interest. Immediate advantages of these new photoresponsive proteins such as genetic encoding, no requirement of chemical modification, and reversibility are paid for by difficulties in predicting the envisaged activity or type and site of domain fusion. In this article, we summarize recent advances and give a survey on currently available design concepts for engineering photoswitchable proteins.
Asunto(s)
Enzimas/química , Enzimas/efectos de la radiación , Ingeniería de Proteínas/métodos , Bacterias/química , Sitios de Unión , Luz , Plantas/química , Dominios ProteicosRESUMEN
The construction of switchable, radiation-controlled, aptameric enzymes - "swenzymes" - is, in principle, feasible. We propose a strategy to make such catalysts from 2 (or more) aptamers each selected to bind specifically to one of the substrates in, for example, a 2-substrate reaction. Construction of a combinatorial library of candidate swenzymes entails selecting a set of a million aptamers that bind one substrate and a second set of a million aptamers that bind the second substrate; the aptamers in these sets are then linked pairwise by a linker, thus bringing together the substrates. In the presence of the substrates, some linked aptamer pairs catalyze the reaction when exposed to external energy in the form of a specific frequency of low-intensity, nonionizing electromagnetic or acoustic radiation. Such swenzymes are detected via a separate product-capturing aptamer that changes conformation on capturing the product; this altered conformation allows it (1) to bind to every potential swenzyme in its vicinity (thereby giving a higher probability of capture to the swenzymes that generate the product) and (2) to bind to a sequence on a magnetic bead (thereby permitting purification of the swenzyme plus product-capturing aptamer by precipitation). Attempts to implement the swenzyme strategy may help elucidate fundamental problems in enzyme catalysis.
Asunto(s)
Aptámeros de Péptidos/metabolismo , Enzimas/química , Enzimas/metabolismo , Biología Sintética , Anticuerpos Catalíticos , Sitios de Unión , Catálisis , Campos Electromagnéticos , Enzimas/efectos de la radiación , Proyectos Piloto , Sonido , Especificidad por SustratoRESUMEN
The bulk of the Earth's biosphere is cold (e.g. 90% of the ocean's waters are ≤ 5°C), sustaining a broad diversity of microbial life. The permanently cold environments vary from the deep ocean to alpine reaches and to polar regions. Commensurate with the extent and diversity of the ecosystems that harbour psychrophilic life, the functional capacity of the microorganisms that inhabitat the cold biosphere are equally diverse. As a result, indigenous psychrophilic microorganisms provide an enormous natural resource of enzymes that function effectively in the cold, and these cold-adapted enzymes have been targeted for their biotechnological potential. In this review we describe the main properties of enzymes from psychrophiles and describe some of their known biotechnological applications and ways to potentially improve their value for biotechnology. The review also covers the use of metagenomics for enzyme screening, the development of psychrophilic gene expression systems and the use of enzymes for cleaning.
Asunto(s)
Biotecnología/métodos , Microbiología Ambiental , Enzimas/metabolismo , Enzimas/efectos de la radiación , Frío , Enzimas/aislamiento & purificaciónAsunto(s)
Proliferación Celular/efectos de la radiación , Enzimas/farmacocinética , Mitocondrias/efectos de la radiación , Fototerapia/métodos , Adenosina Trifosfato/metabolismo , Adenosina Trifosfato/efectos de la radiación , Biología Celular , Complejo IV de Transporte de Electrones/metabolismo , Complejo IV de Transporte de Electrones/efectos de la radiación , Transferencia de Energía , Enzimas/efectos de la radiación , Humanos , Rayos Infrarrojos , Radiación no IonizanteRESUMEN
This paper is a compilation of our findings on non-thermal effects of electromagnetic radiation (EMR) at the molecular level. The outcomes of our studies revealed that that enzymes' activity can be modulated by external electromagnetic fields (EMFs) of selected frequencies. Here, we discuss the possibility of modulating protein activity using visible and infrared light based on the concepts of protein activation outlined in the resonant recognition model (RRM), and by low intensity microwaves. The theoretical basis behind the RRM model expounds a potential interaction mechanism between electromagnetic radiation and proteins as well as protein-protein interactions. Possibility of modulating protein activity by external EMR is experimentally validated by irradiation of the L-lactate Dehydrogenase enzyme.
Asunto(s)
Activación Enzimática/efectos de la radiación , Enzimas/química , Enzimas/efectos de la radiación , Relación Dosis-Respuesta en la Radiación , Campos Electromagnéticos , Estabilidad de Enzimas/efectos de la radiación , Luz , Dosis de RadiaciónRESUMEN
The political upheaval in Germany in 1933 and subsequent movement of medical scholars with the support of the Rockefeller Foundation allowed Manchester to benefit from the arrival of Dr Walter Deutsch, later known as Dr Walter Dale. His research background enabled him to develop a radiobiochemistry laboratory at the Christie Hospital and Holt Radium Institute where he became a world authority on the effects of X-rays on enzymes and also the protective effect of additional solutes. In 1959 he initiated and then edited the International Journal of Radiation Biology. By the time of his retirement in 1962 the strength of his research resulted in his laboratory being recognized by the Medical Research Council.
Asunto(s)
Bioquímica/historia , Biofisica/historia , Radiología/historia , Academias e Institutos/historia , Inglaterra , Enzimas/historia , Enzimas/efectos de la radiación , Alemania , Historia del Siglo XX , Humanos , Publicaciones Periódicas como Asunto/historiaRESUMEN
Photoreactivation of microorganisms following UV disinfection can represent a disadvantage to using UV technology for wastewater treatment since recovery may, in some cases, reach several logs. Thus, decreasing photoreactivation can lead to considerable savings in capital and operating costs. Objectives of this study were to determine pre- and post-UV irradiation conditions which could decrease fecal coliform (FC) photoreactivation in wastewater effluents. Results indicated that delaying exposure to photoreactivating light for 3 h suppressed photoreactivation after relatively low UV doses of 10 and 20 mJ/cm(2). Moreover, at least 440 lux (0.065 mW/cm(2)) of visible light was needed to initiate photoreactivation. Additionally, photoreactivation decreased significantly when samples were exposed to visible light simultaneously or prior to UV irradiation. This was more significantly observed for winter samples, where photoreactivation decreased by nearly 50%. Finally, summer FC populations were more sensitive to inactivation and less able to photoreactivate than winter populations. The effect of visible light on photoreactivation levels may be explained by several photo-mechanisms of FC photolyase, such as photodecomposition of the MTHF co-factor and reduction of FAD.
Asunto(s)
Desinfección/métodos , Enterobacteriaceae/efectos de la radiación , Heces/microbiología , Rayos Ultravioleta , Proteínas Bacterianas/efectos de la radiación , Enzimas/efectos de la radiación , Luz , Viabilidad Microbiana/efectos de la radiación , Contaminantes del AguaRESUMEN
Bio-inspired chemistry based on photoresponsive molecules is a rapidly developing new strategy to mimic the function of various biological systems. The interaction of electromagnetic radiation with molecular systems is ideally suited for the control and powering of dynamic processes at the speed of light. Besides typical applications in artificial photosynthesis, many other aspects, such as the catalytic turnover of substrates or the controlled release or uptake of small bioactive molecules, are readily verified with light-driven model systems. The potential of this novel approach in biomimetic chemistry is briefly explored in this concept article.
Asunto(s)
Enzimas/química , Luz , Biocatálisis , Biomimética , Enzimas/efectos de la radiación , Modelos Biológicos , Oxidación-Reducción , Fotosíntesis , Ribonucleasa Pancreática/química , TermodinámicaRESUMEN
In modelling experiments of the influence of variable magnetic field of industrial frequency (50 Hz) by induction of 1500 and 6000 mkTl during 5 days on microflora and on enzyme activity of soils the South of Russia of different genesis and properties is investigated.
Asunto(s)
Bacterias/efectos de la radiación , Campos Electromagnéticos , Enzimas/efectos de la radiación , Hongos/efectos de la radiación , Microbiología del Suelo , Bacterias/aislamiento & purificación , Bacterias/metabolismo , Estabilidad de Enzimas , Enzimas/metabolismo , Hongos/aislamiento & purificación , Hongos/metabolismo , Federación de Rusia , Suelo/análisisRESUMEN
Although microwave-assisted reactions are widely applied in various domains of organic chemistry, their use in the area of enzyme chemistry has been rather limited, due to the high temperatures associated with the microwave heating: Because current technology, allows a good control of reaction parameters, several examples of microwave-assisted enzyme chemistry have been reported, using stable and effective biocatalysts (modified enzymes). The purpose of this review is to highlight the applications and studies on the influence of microwave irradiation on enzymatic properties and their application in enzyme chemistry.
Asunto(s)
Enzimas/química , Enzimas/efectos de la radiación , Microondas , Catálisis/efectos de la radiación , Solventes/química , TemperaturaRESUMEN
This study is focused on experimental validation of our hypothesis proposed within the Resonant Recognition Model (RRM) [7], [8] that protein function can be modified by an applied electromagnetic radiation of defined frequency in a range of infra red (IR), visible and ultra violet (UV) light. This postulate is investigated here by applying the electromagnetic radiation (1140-1200 nm) to example of L-Lactate Dehydrogenase (LDH) protein and its biological activity is measured before and after the exposures. The presented methodology provides a possibility of enhancing the pharmaceutical and agricultural industries by amplifying drug potency via electromagnetic radiation.
Asunto(s)
Enzimas/metabolismo , Enzimas/efectos de la radiación , Radiación , ADN/genética , ADN/metabolismo , ADN/efectos de la radiación , Activación Enzimática , Cinética , Luz , Modelos Biológicos , NAD/química , NAD/metabolismo , NAD/efectos de la radiación , Proteínas/metabolismo , Proteínas/efectos de la radiaciónAsunto(s)
Enzimas/química , Enzimas/efectos de la radiación , Aerobiosis , Catálisis , Ácido Edético , Peróxido de Hidrógeno/química , Cetonas , Luz , NADP , Oxidación-Reducción , Fotoquímica , EstereoisomerismoRESUMEN
Photochemical regulation of biological processes offers a high level of control to study intracellular mechanisms with unprecedented spatial and temporal resolution. This report summarizes the advances made in recent years, focusing predominantly on the in vivo regulation of gene function using irradiation with UV light. The majority of the described applications entail the utilization of photocaging groups installed either on a small molecule modulator of biomolecular function or directly on a biological macromolecule itself.