<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>1371</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>deu</language>
    <pageFirst>18</pageFirst>
    <pageLast>23</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>10</volume>
    <type>article</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="deu">Vom Wert der Sprache überzeugt sein</title>
    <abstract language="deu">In dem Artikel geht es um die gegenwärtige Sprachsituation im Wissenschaftsbereich in Deutschland u.a. europäischen Ländern. Die sich abzeichnende funktionale Diglossie – Englisch für Gebildete, Landessprachen für den Rest – wirkt sich nachteilig für die Kommunikation zwischen Wissenschaft und Gesellschaft. Besonders systemrelevant ist dabei der Bereich der Hochschullehre. Das sprachliche Abheben des Hochschullehrbetriebes von der Gesellschaft führt zur Desintegration der landeseigenen Bildungselite und schwächt den gesellschaftlichen Zusammenhalt. Für die ausländischen Studierenden und bleibewilligen Absolventen erhöhen rein englischsprachige Studiengänge das Studienabbruchrisiko, sie hemmen ihre Integration und benachteiligen sie auf dem deutschen Arbeitsmarkt. Die absehbaren Folgen einer fehlgeleiteten Sprachenpolitik, die anstelle der akademischen Mehrsprachigkeit die alternativlose Einführung von englischsprachigen Studiengängen an den Hochschulen fördert und dies gleichzeitig zur Internationalisierung verklärt, werden in dem Artikel verdeutlicht.</abstract>
    <parentTitle language="deu">DUZ Wissenschaft &amp; Management</parentTitle>
    <identifier type="issn">2627-0994</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13711</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="SourceTitle">Rösch, O. (2020). Vom Wert der Sprache überzeugt sein. DUZ Wissenschaft &amp; Management, 2020(10), 18–23.</enrichment>
    <licence>Das Dokument ist urheberrechtlich geschützt.</licence>
    <author>Olga Rösch</author>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Wissenschaftssprache Deutsch</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Internationalisierung</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Funktionale Diglossie</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Akademische Mehrsprachigkeit</value>
    </subject>
    <subject>
      <language>deu</language>
      <type>uncontrolled</type>
      <value>Integration</value>
    </subject>
    <collection role="ddc" number="378">Hochschulbildung</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="green_open_access" number="5">Bronze Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1371/WissenschaftsspracheDeutsch-DUZ-10-2020-Roesch.pdf</file>
  </doc>
  <doc>
    <id>1367</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>1097</pageFirst>
    <pageLast>1124</pageLast>
    <pageNumber/>
    <edition/>
    <issue>4</issue>
    <volume>27</volume>
    <type>article</type>
    <publisherName>Casa de Oswaldo Cruz, Fundação Oswaldo Cruz</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">History of the E.I. Martsinovsky Institute of Medical Parasitology and Tropical Medicine: research on malaria and leishmaniasis</title>
    <abstract language="eng">This review presents the 100-year history of the Martsinovsky Institute of Medical Parasitology and Tropical Medicine in Moscow, Russia, starting with its foundation and early activities, and also describes the impact of its leading scientists, some of whom became internationally known. The institute headed a network of nine tropical institutes in the various Soviet republics from the 1920s to 1990. The extensive body of literature on the history and research accomplishments of this institute has mainly been published in Russian; our goal here is to introduce these achievements and this expertise to the international scientific and medical community, focusing on malaria and leishmaniasis and the development of measures to control and monitor these diseases in the USSR.</abstract>
    <parentTitle language="eng">História, Ciências, Saúde – Manguinhos</parentTitle>
    <identifier type="issn">1678-4758</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13675</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="SourceTitle">Strelkova, M., Baranova, A., &amp; Kuhls, K. (2020). History of the E.I. Martsinovsky Institute of Medical Parasitology and Tropical Medicine: research on malaria and leishmaniasis História, Ciências, Saúde – Manguinhos. 27 (4), 1097-1124.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.1590/s0104-59702020000500005</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Margarita V. Strelkova</author>
    <author>Alla M. Baranova</author>
    <author>Katrin Kuhls</author>
    <collection role="ddc" number="570">Biowissenschaften; Biologie</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="green_open_access" number="3">Diamond Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1367/0104-5970-hcsm-27-04-1097.pdf</file>
  </doc>
  <doc>
    <id>1365</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume/>
    <type>conferenceobject</type>
    <publisherName>Schloss Dagstuhl, Leibniz-Zentrum für Informatik</publisherName>
    <publisherPlace>Dagstuhl, Germany</publisherPlace>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Determining All Integer Vertices of the PESP Polytope by Flipping Arcs</title>
    <abstract language="eng">We investigate polyhedral aspects of the Periodic Event Scheduling Problem (PESP), the mathematical basis for periodic timetabling problems in public transport. Flipping the orientation of arcs, we obtain a new class of valid inequalities, the flip inequalities, comprising both the known cycle and change-cycle inequalities. For a point of the LP relaxation, a violated flip inequality can be found in pseudo-polynomial time, and even in linear time for a spanning tree solution. Our main result is that the integer vertices of the polytope described by the flip inequalities are exactly the vertices of the PESP polytope, i.e., the convex hull of all feasible periodic slacks with corresponding modulo parameters. Moreover, we show that this flip polytope equals the PESP polytope in some special cases. On the computational side, we devise several heuristic approaches concerning the separation of cutting planes from flip inequalities. We finally present better dual bounds for the smallest and largest instance of the benchmarking library PESPlib.</abstract>
    <parentTitle language="eng">20th Symposium on Algorithmic Approaches for Transportation Modelling, Optimization, and Systems (ATMOS 2020)</parentTitle>
    <identifier type="isbn">978-3-95977-170-2</identifier>
    <identifier type="issn">2190-6807</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13650</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="SourceTitle">Lindner, N., &amp; Liebchen, C. (2020). Determining All Integer Vertices of the PESP Polytope by Flipping Arcs In Dennis Huisman and Christos D. Zaroliagis, 20th Symposium on Algorithmic Approaches for Transportation Modelling, Optimization, and Systems (ATMOS 2020) (pp. 5:1-5:18). Saarbrücken/Wadern,Germany: Schloss Dagstuhl – Leibniz-Zentrum für Informatik GmbH, Dagstuhl Publishing (OASIcs – OpenAccess Series in Informatics).</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.4230/OASIcs.ATMOS.2020.5</enrichment>
    <licence>Creative Commons - CC BY 3.0 - Namensnennung 3.0 Unported</licence>
    <author>Niels Lindner</author>
    <author>Christian Liebchen</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>periodic event scheduling problem</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>periodic timetabling</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>mixed integer programming</value>
    </subject>
    <collection role="ddc" number="005">Computerprogrammierung, Programme, Daten</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1365/OASIcs-ATMOS-2020-5.pdf</file>
  </doc>
  <doc>
    <id>1364</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>1241</pageFirst>
    <pageLast>1244</pageLast>
    <pageNumber/>
    <edition/>
    <issue>19</issue>
    <volume>32</volume>
    <type>article</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">CMOS-Compatible Silicon Photonic Sensor for Refractive Index Sensing Using Local Back-Side Release</title>
    <abstract language="eng">Silicon photonic sensors are promising candidates for lab-on-a-chip solutions with versatile applications and scalable production prospects using complementary metal-oxide semiconductor (CMOS) fabrication methods. However, the widespread use has been hindered because the sensing area adjoins optical and electrical components making packaging and sensor handling challenging. In this work, a local back-side release of the photonic sensor is employed, enabling a separation of the sensing area from the rest of the chip. This approach allows preserving the compatibility of photonic integrated circuits in the front-end of line and metal interconnects in the back-end of line. The sensor is based on a micro-ring resonator and is fabricated on wafer-level using a CMOS technology. We revealed a ring resonator sensitivity for homogeneous sensing of 106 nm/RIU.</abstract>
    <parentTitle language="eng">IEEE Photonics Technology Letters</parentTitle>
    <identifier type="issn">1941-0174</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13649</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="SourceTitle">Steglich, P., Bondarenko, S., Mai, C., Paul, M., Weller, M., &amp; Mai, A. (2020). CMOS-Compatible Silicon Photonic Sensor for Refractive Index Sensing Using Local Back-Side Release IEEE Photonics Technology Letters. 32 (19), 1241-1244.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.1109/LPT.2020.3019114</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Patrick Steglich</author>
    <author>Siegfried Bondarenko</author>
    <author>Christian Mai</author>
    <author>Martin Paul</author>
    <author>Michael G. Weller</author>
    <author>Andreas Mai</author>
    <collection role="ddc" number="621">Angewandte Physik</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="green_open_access" number="4">Hybrid Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1364/09175013.pdf</file>
  </doc>
  <doc>
    <id>1351</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue>10</issue>
    <volume>8</volume>
    <type>article</type>
    <publisherName>MDPI</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>2020-09-24</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Pepper Bacterial Spot Control by Bacillus velezensis: Bioprocess Solution</title>
    <abstract language="eng">Pepper bacterial spot is one of the most severe plant diseases in terms of infection persistence and economic losses when it comes to fresh pepper fruits used in nutrition and industrial processing. In this study, Bacillus velezensis IP22 isolated from fresh cheese was used as a biocontrol agent of pepper bacterial spot, whose main causal agent is the cosmopolitan pathogen Xanthomonas euvesicatoria. After optimization of the cultivation medium composition aimed at maximizing of the antimicrobial activity against X. euvesicatoria and validation of the optimized medium at the scale of a laboratory bioreactor, in planta tests were performed. The results have showed significant suppression of bacterial spot symptoms in pepper plants by the produced biocontrol agent, as well as reduction of disease spreading on the healthy (uninoculated) pepper leaves. Furthermore, HPLC-MS (high pressure liquid chromatography–mass spectrometry) analysis was employed to examine antimicrobial metabolites produced by B. velezensis IP22, where lipopeptides were found with similar m/z values compared to lipopeptides from fengycin and locillomycin families. The bioprocess solution developed at the laboratory scale investigated in this study represents a promising strategy for production of pepper bacterial spot biocontrol agent based on B. velezensis IP22, a food isolate with a great perspective for application in plant protection.</abstract>
    <parentTitle language="eng">Microorganisms</parentTitle>
    <identifier type="issn">2076-2607</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13510</identifier>
    <enrichment key="opus.import.date">2020-10-08T04:07:41+00:00</enrichment>
    <enrichment key="opus.source">sword</enrichment>
    <enrichment key="opus.import.user">sword</enrichment>
    <enrichment key="opus.import.file">attachment; filename=deposit.zip</enrichment>
    <enrichment key="opus.import.checksum">f38e1de7a5370c7747674e4fffb75406</enrichment>
    <enrichment key="SourceTitle">Pajčin, I., Vlajkov, V., Frohme, M., Grebinyk, S., Grahovac, M., Mojićević, M., et al. (2020). Pepper Bacterial Spot Control by Bacillus velezensis: Bioprocess Solution Microorganisms. 8 (10), 1463.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.3390/microorganisms8101463</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Ivana Pajčin</author>
    <author>Vanja Vlajkov</author>
    <author>Marcus Frohme</author>
    <author>Sergii Grebinyk</author>
    <author>Mila Grahovac</author>
    <author>Marija Mojićević</author>
    <author>Jovana Grahovac</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Xanthomonas euvesicatoria</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>biological control</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>biocontrol agent</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>medium optimization</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>lipopeptide</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>fengycin</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>locillomycin</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>HPLC-MS</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>bioreactor</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>laboratory scale</value>
    </subject>
    <collection role="ddc" number="570">Biowissenschaften; Biologie</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="Import" number="import">Import</collection>
    <collection role="green_open_access" number="1">Gold Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1351/microorganisms-08-01463.pdf</file>
  </doc>
  <doc>
    <id>1356</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue>11</issue>
    <volume>10</volume>
    <type>article</type>
    <publisherName>MDPI</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>0</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>2020-11-20</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Experimental Determination of the Emissivity of Powder Layers and Bulk Material in Laser Powder Bed Fusion Using Infrared Thermography and Thermocouples</title>
    <abstract language="eng">Recording the temperature distribution of the layer under construction during laser powder bed fusion (L-PBF) is of utmost interest for a deep process understanding as well as for quality assurance and in situ monitoring means. While having a notable number of thermal monitoring approaches in additive manufacturing (AM), attempts at temperature calibration and emissivity determination are relatively rare. This study aims for the experimental temperature adjustment of an off-axis infrared (IR) thermography setup used for in situ thermal data acquisition in L-PBF processes. The temperature adjustment was conducted by means of the so-called contact method using thermocouples at two different surface conditions and two different materials: AISI 316L L-PBF bulk surface, AISI 316L powder surface, and IN718 powder surface. The apparent emissivity values for the particular setup were determined. For the first time, also corrected, closer to real emissivity values of the bulk or powder surface condition are published. In the temperature region from approximately 150 °C to 580 °C, the corrected emissivity was determined in a range from 0.2 to 0.25 for a 316L L-PBF bulk surface, in a range from 0.37 to 0.45 for 316L powder layer, and in a range from 0.37 to 0.4 for IN718 powder layer.</abstract>
    <parentTitle language="eng">Metals</parentTitle>
    <identifier type="issn">2075-4701</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13564</identifier>
    <enrichment key="opus.import.date">2020-12-18T16:41:34+00:00</enrichment>
    <enrichment key="opus.source">sword</enrichment>
    <enrichment key="opus.import.user">sword</enrichment>
    <enrichment key="opus.import.file">attachment; filename=deposit.zip</enrichment>
    <enrichment key="opus.import.checksum">93db06043900fc9d5ba75afff449e9b9</enrichment>
    <enrichment key="SourceTitle">Mohr, G., Nowakowski, S., Altenburg, S., Maierhofer, C., &amp; Hilgenberg, K. (2020). Experimental Determination of the Emissivity of Powder Layers and Bulk Material in Laser Powder Bed Fusion Using Infrared Thermography and Thermocouples Metals. 10 (11), 1546.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.3390/met10111546</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Gunther Mohr</author>
    <author>Susanna Nowakowski</author>
    <author>Simon J. Altenburg</author>
    <author>Christiane Maierhofer</author>
    <author>Kai Hilgenberg</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>laser powder bed fusion (L-PBF)</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>selective laser melting (SLM)</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>laser beam melting (LBM)</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>thermography</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>emissivity</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>calibration</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>thermocouples</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>316L</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>IN718</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>process monitoring</value>
    </subject>
    <collection role="ddc" number="620">Ingenieurwissenschaften und zugeordnete Tätigkeiten</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="Import" number="import">Import</collection>
    <collection role="green_open_access" number="1">Gold Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1356/metals-10-01546-v2.pdf</file>
  </doc>
  <doc>
    <id>1363</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>2125</pageFirst>
    <pageLast>2127</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>24</volume>
    <type>article</type>
    <publisherName>Springer Nature</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Coupling biology to electrochemistry—future trends and needs</title>
    <abstract language="eng">The coupling of biological entities with electrodes has already quite some history and has reached a status which is not only based on phenomenological descriptions. Nowadays, we are able to effectively couple redox centres within protein molecules to electrochemical transducers. This allows the transduction of a biochemical reaction into an electrode signal with applications mainly in sensing and bioenergetics [1,2,3,4,5,6,7,8]. However, in most cases, this coupling is not direct, and shuttle molecules or side products of the reaction are used. But also for the direct coupling, significant progress has been made, and several enzymes and redox proteins can be addressed directly by electrodes [8,9,10,11,12,13]. The understanding of the functioning of developed systems is, however, in its infancy. Charge and electrostatic interactions have been mostly studied, and for small dipole molecules such as cytochrome c, the situation can be well described [14]. There is a lack of understanding for more complex enzyme molecules which brings a lot of trial and error into research.</abstract>
    <parentTitle language="eng">Journal of Solid State Electrochemistry</parentTitle>
    <identifier type="issn">1433-0768</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13639</identifier>
    <enrichment key="SourceTitle">Lisdat, F. (2020). Coupling biology to electrochemistry—future trends and needs Journal of Solid State Electrochemistry. 24, 2125–2127.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.1007/s10008-020-04714-y</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Fred Lisdat</author>
    <collection role="ddc" number="541">Physikalische Chemie</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="Funding" number="">Projekt DEAL</collection>
    <collection role="green_open_access" number="4">Hybrid Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1363/Lisdat2020_CouplingBiologyToElectrochemis.pdf</file>
  </doc>
  <doc>
    <id>1362</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>171</pageFirst>
    <pageLast>179</pageLast>
    <pageNumber/>
    <edition/>
    <issue/>
    <volume>2</volume>
    <type>article</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Current limits of structural biology: The transient interaction between cytochrome c6 and photosystem I</title>
    <abstract language="eng">Trimeric photosystem I from the cyanobacterium Thermosynechococcus elongatus (TePSI) is an intrinsic membrane protein, which converts solar energy into electrical energy by oxidizing the soluble redox mediator cytochrome c6 (Cyt c6) and reducing ferredoxin. Here, we use cryo-electron microscopy and small angle neutron scattering (SANS) to characterize the transient binding of Cyt c6 to TePSI. The structure of TePSI cross-linked to Cyt c6 was solved at a resolution of 2.9 Å and shows additional cofactors as well as side chain density for 84% of the peptide chain of subunit PsaK, revealing a hydrophobic, membrane intrinsic loop that enables binding of associated proteins. Due to the poor binding specificity, Cyt c6 could not be localized with certainty in our cryo-EM analysis. SANS measurements confirm that Cyt c6 does not bind to TePSI at protein concentrations comparable to those for cross-linking. However, SANS data indicate a complex formation between TePSI and the non-native mitochondrial cytochrome from horse heart (Cyt cHH). Our study pinpoints the difficulty of identifying very small binding partners (less than 5% of the overall size) in EM structures when binding affinities are poor. We relate our results to well resolved co-structures with known binding affinities and recommend confirmatory methods for complexes with KM values higher than 20 μM.</abstract>
    <parentTitle language="eng">Current Research in Structural Biology</parentTitle>
    <identifier type="issn">2665-928X</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13628</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="SourceTitle">Kölsch, A., Radon, C., Golub, M., Baumert, A., Bürger, J., Mielke, T., et al. (2020). Current limits of structural biology: The transient interaction between cytochrome c6 and photosystem I Current Research in Structural Biology. 2, 171-179.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.1016/j.crstbi.2020.08.003</enrichment>
    <licence>Creative Commons - CC BY-NC-ND - Namensnennung - Nicht kommerziell - Keine Bearbeitungen 4.0 International</licence>
    <author>Adrian Kölsch</author>
    <author>C. Radon</author>
    <author>M. Golub</author>
    <author>A. Baumert</author>
    <author>Jörg Bürger</author>
    <author>Thorsten Mielke</author>
    <author>Fred Lisdat</author>
    <author>Artem Feoktystov</author>
    <author>Jörg Pieper</author>
    <author>Athina Zouni</author>
    <author>Petra Wendler</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>photosystem I</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>cryo-EM</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Thermosynechococcus elongatus</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>small angle neutron scattering</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>cytochrome c6</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>electron transfer</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>photo-biotechnology</value>
    </subject>
    <collection role="ddc" number="570">Biowissenschaften; Biologie</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="green_open_access" number="1">Gold Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1362/1-s2.0-S2665928X20300179-main.pdf</file>
  </doc>
  <doc>
    <id>1360</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst/>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue>12</issue>
    <volume>9</volume>
    <type>article</type>
    <publisherName>MDPI</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>2020-12-09</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Integrative Approach to Phlebotomus mascittii Grassi, 1908: First Record in Vienna with New Morphological and Molecular Insights</title>
    <abstract language="eng">Sand flies (Diptera: Psychodidae: Phlebotominae) are blood-feeding insects that transmit the protozoan parasites Leishmania spp. and various arthropod-borne (arbo) viruses. While in Mediterranean parts of Europe the sand fly fauna is diverse, in Central European countries including Austria mainly Phlebotomus mascittii is found, an assumed but unproven vector of Leishmania infantum. To update the currently understudied sand fly distribution in Austria, a sand fly survey was performed and other entomological catches were screened for sand flies. Seven new trapping locations of Ph. mascittii are reported including the first record in Vienna, representing also one of the first findings of this species in a city. Morphological identification, supported by fluorescence microscopy, was confirmed by two molecular approaches, including sequencing and matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS) protein profiling. Sand fly occurrence and activity were evaluated based on surveyed locations, habitat requirements and climatic parameters. Moreover, a first comparison of European Ph. mascittii populations was made by two marker genes, cytochrome c oxidase subunit 1 (COI), and cytochrome b (cytb), as well as MALDI-TOF mass spectra. Our study provides new important records of Ph. mascittii in Austria and valuable data for prospective entomological surveys. MALDI-TOF MS protein profiling was shown to be a reliable tool for differentiation between sand fly species. Rising temperatures and globalization demand for regular entomological surveys to monitor changes in species distribution and composition. This is also important with respect to the possible vector competence of Ph. mascittii.</abstract>
    <parentTitle language="eng">Pathogens</parentTitle>
    <identifier type="issn">2076-0817</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13600</identifier>
    <enrichment key="opus.import.date">2021-01-07T20:33:36+00:00</enrichment>
    <enrichment key="opus.source">sword</enrichment>
    <enrichment key="opus.import.user">sword</enrichment>
    <enrichment key="opus.import.file">attachment; filename=deposit.zip</enrichment>
    <enrichment key="opus.import.checksum">c5d4ca62bc69ec16005f22f0a3057506</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.3390/pathogens9121032</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Edwin Kniha</author>
    <author>Vít Dvořák</author>
    <author>Petr Halada</author>
    <author>Markus Milchram</author>
    <author>Adelheid G. Obwaller</author>
    <author>Katrin Kuhls</author>
    <author>Susanne Schlegel</author>
    <author>Martina Köhsler</author>
    <author>Wolfgang Poeppl</author>
    <author>Karin Bakran-Lebl</author>
    <author>Hans-Peter Fuehrer</author>
    <author>Věra Volfová</author>
    <author>Gerhard Mooseder</author>
    <author>Vladimir Ivovic</author>
    <author>Petr Volf</author>
    <author>Julia Walochnik</author>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Transphlebotomus</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>Central Europe</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>autoimmunofluorescence</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>MALDI-TOF mass spectrometry</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>genotyping</value>
    </subject>
    <subject>
      <language>eng</language>
      <type>uncontrolled</type>
      <value>leishmaniasis</value>
    </subject>
    <collection role="ddc" number="570">Biowissenschaften; Biologie</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="Import" number="import">Import</collection>
    <collection role="green_open_access" number="1">Gold Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1360/pathogens-09-01032-v3.pdf</file>
  </doc>
  <doc>
    <id>1359</id>
    <completedYear>2020</completedYear>
    <publishedYear/>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>e1008095</pageFirst>
    <pageLast/>
    <pageNumber/>
    <edition/>
    <issue>9</issue>
    <volume>16</volume>
    <type>article</type>
    <publisherName/>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>1</belongsToBibliography>
    <completedDate>--</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Ten simple rules on how to write a standard operating procedure</title>
    <abstract language="eng">Research publications and data nowadays should be publicly available on the internet and, theoretically, usable for everyone to develop further research, products, or services. The long-term accessibility of research data is, therefore, fundamental in the economy of the research production process. However, the availability of data is not sufficient by itself, but also their quality must be verifiable. Measures to ensure reuse and reproducibility need to include the entire research life cycle, from the experimental design to the generation of data, quality control, statistical analysis, interpretation, and validation of the results. Hence, high-quality records, particularly for providing a string of documents for the verifiable origin of data, are essential elements that can act as a certificate for potential users (customers). These records also improve the traceability and transparency of data and processes, therefore, improving the reliability of results. Standards for data acquisition, analysis, and documentation have been fostered in the last decade driven by grassroot initiatives of researchers and organizations such as the Research Data Alliance (RDA). Nevertheless, what is still largely missing in the life science academic research are agreed procedures for complex routine research workflows. Here, well-crafted documentation like standard operating procedures (SOPs) offer clear direction and instructions specifically designed to avoid deviations as an absolute necessity for reproducibility.&#13;
&#13;
Therefore, this paper provides a standardized workflow that explains step by step how to write an SOP to be used as a starting point for appropriate research documentation.</abstract>
    <parentTitle language="eng">PLoS Computational Biology</parentTitle>
    <identifier type="issn">1553-7358</identifier>
    <identifier type="urn">urn:nbn:de:kobv:526-opus4-13598</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="SourceTitle">Hollmann, S., Frohme, M., Endrullat, C., Kremer, A., D’Elia, D., Regierer, B., et al. (2020). Ten simple rules on how to write a standard operating procedure PLoS Computational Biology. 16 (9), e1008095.</enrichment>
    <enrichment key="DOI_VoR">https://doi.org/10.1371/journal.pcbi.1008095</enrichment>
    <licence>Creative Commons - CC BY - Namensnennung 4.0 International</licence>
    <author>Susanne Hollmann</author>
    <author>Marcus Frohme</author>
    <author>Christoph Endrullat</author>
    <author>Andreas Kremer</author>
    <author>Domenica D'Elia</author>
    <author>Babette Regierer</author>
    <author>Alina Nechyporenko</author>
    <collection role="ddc" number="570">Biowissenschaften; Biologie</collection>
    <collection role="institutes" number="">Fachbereich Ingenieur- und Naturwissenschaften</collection>
    <collection role="open_access" number="">open_access</collection>
    <collection role="green_open_access" number="1">Gold Open Access</collection>
    <thesisPublisher>Technische Hochschule Wildau</thesisPublisher>
    <file>https://opus4.kobv.de/opus4-th-wildau/files/1359/pcbi.1008095.pdf</file>
  </doc>
</export-example>
