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Im Vergleich zu anderen deutschen Hochschulen begann die Ausbildung von Studierenden der Zahnheilkunde in Greifswald relativ spät. Seit dem Wintersemester 1893/94 führte der Greifswalder Zahnarzt Hermann Bahls fakultative zahnärztliche Spezialkurse für Medizinstudierende an der Chirurgischen Universitätsklinik durch. Erst am 12. Dezember 1900 wurde dann das zahnärztliche Institut an der Greifswalder Universität unter dem Dach der Chirurgischen Universitätsklinik eröffnet.
Als erster Leiter wurde Hermann Schröder noch in seiner Eigenschaft als Assistent der Chirurgischen Universitätsklinik eingesetzt. Unter der Leitung von Hermann Schröder (1900-1907), Guido Fischer (1907-1911) und Paul Adloff (1911-1920) entwickelte sich das zahnärztliche Institut zu einem anerkannten Glied der Medizinischen Fakultät der Greifswalder Universität.
Ab dem 15. April 1916 durfte das bisher der Chirurgischen Klinik zugeordnete zahnärztliche Institut als selbständige Einrichtung der Universität geführt werden.
Mit Erich Becker (1920-1923) und Friedrich Proell (1923-1935) entwickelte sich das Greifswalder zahnärztliche Institut in den zwanziger Jahren zum viertgrößten zahnärztlichen Universitätsinstitut in Deutschland. Die Bemühungen der Institutsleiter lagen immer in der Gewährleistung der Ausbildung der Studierenden, der baulichen Erweiterung des Institutes und der technischen Verbesserung. Erst 1934 wurde das Institut im Gebäude der Rotgerberstraße 8 zusammengefasst, nachdem es zeitweilig in drei verschiedenen Häusern, ab 1901 Hunnenstraße 1, ab 1928 Hunnenstraße 31 und ab 1931 Stralsunder Straße 10, untergebracht war.
Paul Wustrow (1936-1945) wollte die Einheit von Lehre, Forschung und medizinischer Betreuung fortführen, doch der Ausbruch des 2.Weltkrieges behinderte diese Fortführung. Schwerste Kriegsverletzungen mit Kieferbrüchen und Kieferschüssen machte die Einrichtung einer Kieferchirurgischen Bettenstation notwendig. Diese entstand unter Wustrow noch im Januar 1945.
Nach Kriegsende und dem Suizid von Wustrow wurde die Zahnklinik in kurzer Abfolge durch Richard Plötz (1945-1946), Georg Packhäuser (1946-1946) und Karl Jarmer (1946-1947) geleitet, bis Otto Hübner (1947-1952) als neuer Direktor ins Amt trat.
Josef Heiss (1952-1953) übernahm nach Hübner die Leitung der Zahnklinik und forschte intensiv über die chirurgische Wiederherstellung des Alveolarkammes. Gerd Staegemann arbeitete als Assistent unter der Leitung von Heiss und beschäftigte sich auch intensiv mit der Problematik der Fremdkörperwirkung. Unter der Leitung von Richard Plötz (1953-1963) wurden für die zahnärztliche Chirurgie Operationsstühle angeschafft und ein Operationsraum eingerichtet.
1963 übernahm Albrecht Schönberger (1963-1993) 30 Jahre die Leitung der Klinik und Poliklinik für Zahn-Mund- und Kieferheilkunde. Es entstand ein Neubau für die Klinik der Mund-Kiefer- und Gesichtschirurgie im Klinikumskomplex in der Sauerbruchstraße, welcher im April 1992 bezogen wurde.
Nach Schönberger übernahm Hans-Robert Metelmann (1993-2020) den Lehrstuhl und das Direktorat der Klinik und Poliklinik für Mund- Kiefer- und Gesichtschirurgie in Greifswald. Lokalisiert an zwei Standorten fungieren die Oralchirurgie und die Mund-Kiefer- und Gesichtschirurgie unverändert als eine Einheit an der Universitätsmedizin in Greifswald.
Die enossale Implantologie begann in Greifswald mit Gerd Staegemann, der die Methode der geschlossenen enossalen Implantologie als sogenannte Stiftverbolzung bzw. transdentale Fixation erforschte und publizierte. Die transdentale Fixation als eine Form der geschlossenen enossalen Implantation war seit den 50iger an der Greifswalder Zahnklinik eine übliche und erfolgreiche Behandlungsmethode.
Ab 1983 forschten die Greifswalder Universitätszahnärzte im Sinne einer Prüfklinik zur Anwendung der Titanblattimplantate des Typs Leipzig als offenes enossales Implantationsverfahren. Die politische Wende in Deutschland brachte auch für die Greifswalder Zahnklinik eine schnelle Weiterentwicklung der offenen enossalen Implantologie.
Die Behandlungsmethoden wurden weiter verbessert und die Produktpalette der Implantatsysteme maßgeblich erweitert. Wobei insbesondere die ITI-Straumann- Implantate und die Ankylos- Implantate erfolgreich zur implantologischen Therapie zum Einsatz kamen.
Die sich vollziehenden Veränderungen in der deutschen Zahnmedizin sind nicht vorwiegend struktureller sondern vor allem inhaltlicher Art. Daher wurde und muss die Ausbildung der Zahnmedizinstudierenden immer wieder angepasst werden, insbesondere die Implantologie als junge Teildisziplin fand Eingang in die studentische Ausbildung.
Die Fort- und Weiterbildungen in Form der Greifswalder Fachsymposien und der Curricula in der Implantologie sind ein weiterer wichtiger Baustein der Aktivitäten in der Universitätszahnmedizin Greifswald.
Heute blickt die Greifswalder Zahnklinik auf mehr als 125 Jahre erfreuliche Entwicklungen in der zahnärztlichen Chirurgie und davon 65 Jahre erfolgreiche Implantologie zurück.
Nowadays, a challenge in wildlife management and nature conservation is to reach a state of human-wildlife coexistence, integrating wildlife into the human-dominated landscape. Achieving a state of coexistence is urgent as human-wildlife conflicts increase over time. Thus a "route guide" for researchers and conservation practitioners will be needed to identify if a human-wildlife interaction is heading towards conflict or coexistence, enabling them to conduct management activities, when possible, to achieve human-wildlife coexistence. Researchers have used different individual-based attributes as a proxy to measure support towards wildlife species by the general public. Different operationalizations from Environmental Economics and Environmental and Conservation Psychology research fields have been used to measure support. Examples of operationalization are the willingness-to-pay and Likert-type scale, or rating scale, from the first and second research fields. In the first, participants must indicate how much they would be willing to pay to protect a specific wildlife species population in a particular area and time. In the second, participants are asked to rate statements through, e.g., a five-point ordinal rating scale with opposite alternatives between, e.g., strongly agree and strongly disagree. In the human dimension of natural resources management research, variations of these methodologies have been used to measure support, not only for one wildlife species but for a set. For the willingness-to-pay variation, i.e., money allocation, participants must distribute a constant sum of money among a set of wildlife species. For the rating scale variation, each of the wildlife species in the set corresponds to a statement to be rated. The thesis aims to contrast these two variations, i.e., money allocation and rating scale, in their capacity to assess support changes towards a set of 12 native wildlife species from different taxa.
A survey was applied in 2018 (n: 368) and replicated in 2019 (n: 359) among urban dwellers who cohabit with the wildlife species set, in Valdivia, south of Chile. The surveys were applied before and after information disclosure and exposure in an experimental and longitudinal research design structure, respectively. As information disclosure, the threatened and endemic status of the wildlife species was presented to the participants. On the other hand, mass media coverage of a human-wildlife conflict involving one of the species included in study, the South American Sea Lion, was used for information exposure. The results indicate that the money allocation method identified support changes among the wildlife species to a greater extent than the rating scale for both types of information (Chapters 2, 3, and 4). The money allocation in the experimental design structure grouped the wildlife species based on their threatened and endemic status, while the rating scale did not come with the same results (Chapter 3). In the longitudinal design structure, the South American Sea Lion support decreased based on the average values of the money allocation and rating scale after the information exposure (Chapter 4). Differently, when the South American Sea Lion position support is compared with the other wildlife species, based on the money allocation, there was a descent, while the rating scale presented an ascent after the mass media coverage of the human-wildlife conflict (Chapter 4). This difference between the results of the two methods, in both research design structures, can be explained to a certain extent due to their scaling technique characteristics. The money allocation is a comparative scale; therefore, the support given to one wildlife species will affect the possible support given to the other species. In contrast, the rating scale is a non-comparative scale, i.e., the support given to a wildlife species is independent of the support given to the other wildlife species in the set. In the experimental research design structure (Chapters 2 and 3), to give or increase the support to a threatened or endemic wildlife species, a bill should be taken from another wildlife species, usually not threatened nor endemic. On the contrary, in the rating scale, there was no need to choose; the support could be increased for a wildlife species without decreasing the support for other wildlife species. In the longitudinal study design structure, the money allocation allows direct comparison between wildlife species from one year to another, while the rating scale does not. For the money allocation, the possible amount of support to be given to a wildlife species, i.e., 12 bills of 1,000 CLP each, did not vary from 2018 to 2019. For the rating scale, the values received among the wildlife species can vary within the rating scale from one year to another, misleading to incorrect interpretations. The money allocation method can be suitable for monitoring human-wildlife interactions, i.e., to position and visualize support shifts. The money allocation could be used as an overview of human-wildlife interactions in a specific area, working as a first assessment.
Pentathiepins are cyclic polysulfides that exert antiproliferative and cytotoxic activity in cancer cells, induce oxidative stress and apoptosis, and potently inhibit GPx1. These properties render this class of compounds promising candidates for the development of anticancer drugs. However, the biological effects and how they intertwine to promote high cytotoxicity have not been systematically assessed throughout a panel of cancer cell lines from distinct tissues of origin. In this thesis, six novel pentathiepins were analyzed and constitute the second generation of compounds with additional properties such as fluorescence or improved water solubility to facilitate cellular testing. All compounds underwent extensive biological evaluation in 14 human cancer cell lines. These studies included investigations of the inhibitory potential with regards to GPx1 and cell proliferation, examined the cytotoxicity in human cancer cell lines, as well as the induction of oxidative stress and DNA strand breaks. Furthermore, selected hallmarks of apoptosis, ferroptosis, and autophagy were studied. Experimental approaches regarding these cellular mechanisms included observing morphological changes, detecting phosphatidyl serine exposure and caspase activity, and quantifying cleaved PARP1 and levels of LC3B II. In addition, the analysis of the cell cycle aimed to identify aberrations or arrests in cell division.
Five of the six tested pentathiepins proved to be potent inhibitors of the GPx1, while all six exerted high cytotoxic and antiproliferative activity, although to different extents. There was a clear connection observed between the potential to provoke oxidative stress and damage to DNA in the form of single- and double-strand breaks both extra- and intracellularly. Furthermore, various experiments supported apoptosis but not ferroptosis as the mechanism of cell death in four different cell lines. In particular, the externalization of PS, the detection of activated caspases, and the cleavage of PARP1 corroborated this conclusion. Additionally, indications for autophagy were found, but more investigations are required to verify the current data. The findings of this dissertation are mainly in line with the postulated mechanism of action proposed for pentathiepins and a previous publication from our group that described their biological activity. However, the influence of modulators such as oxygen and GSH on the biological effects was ambiguous and dependent on the compound. The expression profile of the cell lines concerning GPx1 and CAT did not influence the cellular response toward the treatment, whereas the cell doubling time correlated with the cytotoxicity.
As the various pentathiepins give rise to different biological responses, modulation of the biological effects depends on the distinct chemical structures fused to the sulfur ring. This may allow for future optimization of the anticancer activity of pentathiepins. An analysis of the structure-activity relationships revealed that the piperazine scaffold was associated with superior biological activity compared to the pyrrolo-pyrazine backbone. Furthermore, substituents with electron-withdrawing properties or those providing a free electron pair, such as fluorine or morpholine, were advantageous. These findings should help design and synthesize the next generation of pentathiepins, thereby expanding the library of compounds, allowing for the further deduction of structure-activity relationships and an improved understanding of their mechanism of action.
Background
The Federal Ministry of Education and Research of Germany (BMBF) funds a network of university medicines (NUM) to support COVID-19 and pandemic research at national level. The “COVID-19 Data Exchange Platform” (CODEX) as part of NUM establishes a harmonised infrastructure that supports research use of COVID-19 datasets. The broad consent (BC) of the Medical Informatics Initiative (MII) is agreed by all German federal states and forms the legal base for data processing. All 34 participating university hospitals (NUM sites) work upon a harmonised infrastructural as well as legal basis for their data protection-compliant collection and transfer of their research dataset to the central CODEX platform. Each NUM site ensures that the exchanged consent information conforms to the already-balloted HL7 FHIR consent profiles and the interoperability concept of the MII Task Force “Consent Implementation” (TFCI). The Independent Trusted Third-Party (TTP) of the University Medicine Greifswald supports data protection-compliant data processing and provides the consent management solutions gICS.
Methods
Based on a stakeholder dialogue a required set of FHIR-functionalities was identified and technically specified supported by official FHIR experts. Next, a “TTP-FHIR Gateway” for the HL7 FHIR-compliant exchange of consent information using gICS was implemented. A last step included external integration tests and the development of a pre-configured consent template for the BC for the NUM sites.
Results
A FHIR-compliant gICS-release and a corresponding consent template for the BC were provided to all NUM sites in June 2021. All FHIR functionalities comply with the already-balloted FHIR consent profiles of the HL7 Working Group Consent Management. The consent template simplifies the technical BC rollout and the corresponding implementation of the TFCI interoperability concept at the NUM sites.
Conclusions
This article shows that a HL7 FHIR-compliant and interoperable nationwide exchange of consent information could be built using of the consent management software gICS and the provided TTP-FHIR Gateway. The initial functional scope of the solution covers the requirements identified in the NUM-CODEX setting. The semantic correctness of these functionalities was validated by project-partners from the Ludwig-Maximilian University in Munich. The production rollout of the solution package to all NUM sites has started successfully.
Diagenetic illite growth in porous sandstones leads to significant modifications of the initial pore system which result in tight reservoirs. Understanding and quantifying these changes provides insight into the porosity-permeability history of the reservoir and improves predictions on petrophysical behavior. To characterize the various stages of diagenetic alteration, a focused ion beam – scanning electron microscopy (FIB-SEM) study was undertaken on aeolian sandstones from the Bebertal outcrop of the Parchim Formation (Early Permian Upper Rotliegend group). Based on 3D microscopic reconstructions, three different textural types of illite crystals occur, common to many tight Rotliegend sandstones, namely (1) feldspar grain alterations and associated illite meshworks, (2) tangential grain coats, and (3) pore-filling laths and fibers. Reaction textures, pore structure quantifications, and numerical simulations of fluid transport have revealed that different generations of nano-porosity are connected to the diagenetic alteration of feldspars and the authigenic growth of pore-filling illites. The latter leads to the formation of microstructures that range from authigenic compact tangential grain coatings to highly porous, pore-filling structures. K-feldspar replacement and initial grain coatings of illite are composed primarily of disordered 1Md illite whereas the epitaxially grown illite lath- and fiber-shaped crystals occurring as pore-filling structures are of the trans-vacant 1Mtv polytype. Although all analyzed 3D structures offer connected pathways, the largest reduction in sandstone permeability occurred during the initial formation of the tangential illite coatings that sealed altered feldspars and the subsequent growth of pore-filling laths and fibrous illites. Analyses of both illite pore-size and crystallite-size distributions indicate that crystal growth occurred by a continuous nucleation and growth mechanism probably controlled by the multiple influx of potassium-rich fluids during late Triassic and Jurassic times. The detailed insight into the textural varieties of illite crystal growth and its calculated permeabilities provides important constraints for understanding the complexities of fluid-flow in tight reservoir sandstones.
Lacewings (Neuroptera) have predatory larvae with highly specialised mouthparts. Larvae of many groups within Neuroptera are well represented as fossils preserved in ambers; however, larvae of some groups are less often reported in the literature. Here we report such a rare case, a larva of the group Hemerobiidae, an aphidlion, preserved in a piece of Eocene Baltic amber (about 40 million years old). It is preserved together with three possible prey items, wingless aphids, most likely representatives of Germaraphis (or at least closely related to this group). The aphidlion can be identified based on the morphology of the antennae, simple curved and toothless stylets, well developed labial palps, and the absence of other mouth-part structures such as a protruding labrum or maxillary palps. A long, club-shaped distal element of the labial palps identifies the specimen as a larva of Hemerobiidae. The aphids can be identified based on their very long, beak-like mouth parts. This find is, to our knowledge, the first example of a lacewing larva preserved together with its potential prey. We briefly discuss other cases in which fossils preserved in amber allow us to reconstruct aspects of behaviour and interactions of fossil lacewing larvae.
Forest ecosystems around the world and especially boreal forests, are facing
drastically changing climatic conditions. It is known that these changes could
challenge their functionality and vitality. Still, the exact impact is not fully
understood, as tree growth is a complex process and depends on countless
environmental and genetic factors. To estimate the effects of climate change
on tree growth and forest development precisely, we must learn more about
tree growth itself. A comprehensive approach is needed where trees and
forests are investigated on different scales and levels of detail, ranging from
global studies to studies on single individuals.
In this dissertation, I follow such a comprehensive approach, using the
North American conifer white spruce as an example. I present three papers
in the form of three chapters in which my co-authors and I studied the
growth and anatomy of white spruce (Picea glauca [Moench] Voss) and how
it is influenced by environmental, climatic, and genetic factors.
We used diverse approaches and methods on different spatial scales, ranging from
investigations on the landscape to the local scale. We established three paired
plots with forest and treeline sites (two cold-limited and one drought-limited).
as well as one additional forest site. In the first chapter, we concentrated
on the genetic diversity of white spruce within and between populations at
all study sites throughout Alaska. The genetic investigations were combined
with analyses on the individual growth response of trees to climatic conditions
to find whether genetic similarities or spatial proximity caused similarities
in growth and climatic sensitivity. In the second chapter, we studied the
direct and indirect effects of environmental conditions on the xylem tissue
of white spruce. We analyzed the impact of precipitation, temperature, and
tree height on four xylem anatomical traits in trees growing at the three
treelines. The investigated traits represented the main functions of xylem
tissue (i.e., water transport and structural support). In the third chapter,
we investigated similar xylem anatomical traits at one cold-limited treeline.
We compared xylem anatomy and annual increment between genetic groups
and individuals and between spatial groups to investigate whether spatial or
genetic grouping influenced the anatomy and growth of white spruce.
We found an overall high gene flow and high genetic diversity in white
spruce. However, the sensitivity of the growth and anatomical traits of white
spruce was driven mainly by spatial rather than genetic effects and differed
between study sites. Trees from the drought-limited site were more sensitive
towards precipitation and a moisture index, while trees from the cold-limited
sites were more sensitive towards temperature. A strong direct effect of tem-
perature was primarily found in latewood traits related to the structural sup-
port of the tree. Earlywood traits related to water transport, however, were
influenced mainly by tree height. Tree height itself was potentially affected
by diverse abiotic and biotic factors (e.g., (micro)climate, soil conditions,
and competition). Thus, traits related to water transport were indirectly
influenced by environmental conditions. Genetic effects in xylem anatomical
traits were found in the earlywood hydraulic diameter and latewood den-
sity, whereas in general, primarily spatial rather than genetic grouping was
influencing the anatomy of white spruce.
Overall, white spruce showed to be a genetically diverse species with a
high gene flow. The effects of spatial proximity and spatial grouping on the
sensitivity and anatomy of white spruce indicate high phenotypic plastic-
ity. This high phenotypic plasticity combined with the vast genetic diversity
translates into an immense potential for the species to adjust (phenotypically)
and possibly adapt (genetically) to changing conditions. Thus, in terms of
climate change, white spruce may be a rather persistent species that manages
to cope with the drastic changes. Though additional work might be needed to
draw a more solid conclusion, the presented work shows how a comprehensive
study approach can help to interpret and understand the growth and ecology
of a tree species. It may be an inspiration for future studies to broaden their
approaches and to use comprehensive methods on different levels of detail to
not only observe trees but to explore and understand them.
Fast screening of enzyme variants is crucial for tailoring biocatalysts for the asymmetric synthesis of non-natural chiral chemicals, such as amines. However, most existing screening methods either are limited by the throughput or require specialized equipment. Herein, we report a simple, high-throughput, low-equipment dependent, and generally applicable growth selection system for engineering amine-forming or converting enzymes and apply it to improve biocatalysts belonging to three different enzyme classes. This results in (i) an amine transaminase variant with 110-fold increased specific activity for the asymmetric synthesis of the chiral amine intermediate of Linagliptin; (ii) a 270-fold improved monoamine oxidase to prepare the chiral amine intermediate of Cinacalcet by deracemization; and (iii) an ammonia lyase variant with a 26-fold increased activity in the asymmetric synthesis of a non-natural amino acid. Our growth selection system is adaptable to different enzyme classes, varying levels of enzyme activities, and thus a flexible tool for various stages of an engineering campaign.
Target proteins in biotechnological applications are highly diverse. Therefore, versatile flexible expression systems for their functional overproduction are required. In order to find the right heterologous gene expression strategy, suitable host-vector systems, which combine different genetic circuits, are useful. In this study, we designed a novel Bacillus subtilis expression toolbox, which allows the overproduction and secretion of potentially toxic enzymes. This toolbox comprises a set of 60 expression vectors, which combine two promoter variants, four strong secretion signals, a translation-enhancing downstream box, and three plasmid backbones. This B. subtilis toolbox is based on a tailor-made, clean deletion mutant strain, which is protease and sporulation deficient and exhibits reduced autolysis and secondary metabolism. The appropriateness of this alternative expression platform was tested for the overproduction of two difficult-to-produce eukaryotic model proteins. These included the sulfhydryl oxidase Sox from Saccharomyces cerevisiae, which forms reactive hydrogen peroxide and undesired cross-linking of functional proteins, and the human interleukin-1β, a pro-inflammatory cytokine. For the best performing Sox and interleukin, overproducing and secreting variants of these new B. subtilis toolbox fermentation strategies were developed and tested. This study demonstrates the suitability of the prokaryotic B. subtilis host-vector system for the extracellular production of two eukaryotic proteins with biotechnological relevance.
Introduction
Neurofilament light (NfL) can be detected in blood of healthy individuals and at elevated levels in those with different neurological diseases. We investigated if the choice of biological matrix can affect results when using NfL as biomarker in epidemiological studies.
Method
We obtained paired serum and EDTA-plasma samples of 299 individuals aged 37–67 years (BiDirect study) and serum samples of 373 individuals aged 65–83 years (MEMO study). In BiDirect, Passing–Bablok analyses were performed to assess proportional and systematic differences between biological matrices. Associations between serum or EDTA-plasma NfL and renal function (serum creatinine, serum cystatin C, glomerular filtration rate, and kidney disease) were investigated using linear or logistic regression, respectively. All regression coefficients were estimated (1) per one ng/L increase and (2) per one standard deviation increase (standardization using z-scores). In MEMO, regression coefficients were estimated (1) per one ng/L increase of serum or calculated EDTA-plasma NfL and (2) per one standard deviation increase providing a comparison to the results from BiDirect.
Results
We found proportional and systematic differences between paired NfL measurements in BiDirect, i.e., serum NfL [ng/L] = −0.33 [ng/L] + 1.11 × EDTA-plasma NfL [ng/L]. Linear regression coefficients for the associations between NfL and renal function did not vary between the different NfL measurements. In MEMO, one standard deviation increase in serum NfL was associated with greater changes in the outcomes than in BiDirect.
Conclusion
Although there are differences between serum and EDTA-plasma NfL, results can be used interchangeably if standardized values are used.