Relevant bibliographies by topics / Luciferine

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Luciferine'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Luciferine"

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Amat, Albert, Josepa Rigau, Renata Nicolau, et al. "Effect of red and near-infrared laser light on adenosine triphosphate (ATP) in the luciferine–luciferase reaction." Journal of Photochemistry and Photobiology A: Chemistry 168, no. 1-2 (2004): 59–65. http://dx.doi.org/10.1016/j.jphotochem.2004.05.024.

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Studetsov, Evgeniy P., Olga V. Neporozhneva, Anna A. Golovina, Natalya I. Novikova, Viktoriya V. Orlovskaya, and Stanislav M. Ramsh. "ELABORATION OF THE TECHNOLOGY FOR PRERARATION OF SYNTHETIC D-LUCIFERINE AND ITS CORE INTERMEDIATES (review)." Bulletin of the Saint Petersburg State Institute of Technology (Technical University) 34, no. 60 (2016): 49–57. http://dx.doi.org/10.15217/issn1998984-9.2016.34.49.

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Rautemaa, Riina, Gary A. Jarvis, Pertti Marnila, and Seppo Meri. "Acquired Resistance of Escherichia coli to Complement Lysis by Binding of Glycophosphoinositol-Anchored Protectin (CD59)." Infection and Immunity 66, no. 5 (1998): 1928–33. http://dx.doi.org/10.1128/iai.66.5.1928-1933.1998.

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ABSTRACT Protectin (CD59) is a glycophosphoinsitol (GPI)-anchored defender of human cells against lysis by the membrane attack complex of complement. In this study, we examined whether protectin released from human cell membranes can incorporate into the surface of gram-negative bacteria. Analysis by using radiolabeled protectin, immunofluorescence, flow cytometry, and whole-cell enzyme-linked immunosorbent assay demonstrated that protectin bound to nonencapsulated Escherichia coli EH237 (Re) and EH234 (Ra) in a calcium-dependent manner. The incorporation required the GPI-phospholipid moiety s
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Kotlobay, Alexey A., Maxim A. Dubinnyi, Konstantin V. Purtov, et al. "Bioluminescence chemistry of fireworm Odontosyllis." Proceedings of the National Academy of Sciences 116, no. 38 (2019): 18911–16. http://dx.doi.org/10.1073/pnas.1902095116.

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Marine polychaetes Odontosyllis undecimdonta, commonly known as fireworms, emit bright blue-green bioluminescence. Until the recent identification of the Odontosyllis luciferase enzyme, little progress had been made toward characterizing the key components of this bioluminescence system. Here we present the biomolecular mechanisms of enzymatic (leading to light emission) and nonenzymatic (dark) oxidation pathways of newly described O. undecimdonta luciferin. Spectral studies, including 1D and 2D NMR spectroscopy, mass spectrometry, and X-ray diffraction, of isolated substances allowed us to ch
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Delroisse, Jérôme, Esther Ullrich-Lüter, Stefanie Blaue, et al. "A puzzling homology: a brittle star using a putative cnidarian-type luciferase for bioluminescence." Open Biology 7, no. 4 (2017): 160300. http://dx.doi.org/10.1098/rsob.160300.

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Bioluminescence relies on the oxidation of a luciferin substrate catalysed by a luciferase enzyme. Luciferins and luciferases are generic terms used to describe a large variety of substrates and enzymes. Whereas luciferins can be shared by phylogenetically distant organisms which feed on organisms producing them, luciferases have been thought to be lineage-specific enzymes. Numerous light emission systems would then have co-emerged independently along the tree of life resulting in a plethora of non-homologous luciferases. Here, we identify for the first time a candidate luciferase of a luminou
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Sala, Rossano. "Omaggio a Pietro Barcellona. Uomo e profeta del nostro tempo." Salesianum 76, no. 3 (2014): 465–96. https://doi.org/10.63343/wd7159qc.

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L’articolo ripropone sinteticamente l’itinerario intellettuale di Pietro Barcellona, pensatore significativo del panorama culturale e politico italiano. L’intenzione principale del filosofo siciliano è quella di mettere a fuoco la drammatica emergenza antropologica che caratterizza il nostro tempo: attraverso una serrata analisi critica delle radici luciferine della modernità e dei suoi inquietanti esiti insieme post-moderni e post-umani, egli cerca di creare le basi per il ritorno ad un pensiero antropologico a tutto tondo. La riscoperta fenomenologica dello statuto filiale dell’umano – gener
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Jones, Krysten A., William B. Porterfield, Colin M. Rathbun, David C. McCutcheon, Miranda A. Paley, and Jennifer A. Prescher. "Orthogonal Luciferase–Luciferin Pairs for Bioluminescence Imaging." Journal of the American Chemical Society 139, no. 6 (2017): 2351–58. http://dx.doi.org/10.1021/jacs.6b11737.

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Rachman, A. R. Abdul, Noor Azmi Shaharuddin, M. K. Sabullah, and M. Y. Shukor. "In silico study to breaking mystery of bioluminescence protein structure of bacterial luciferase and firefly luciferase." Bulletin of Environmental Science and Sustainable Management (e-ISSN 2716-5353) 2, no. 1 (2014): 17–23. http://dx.doi.org/10.54987/bessm.v2i1.115.

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Bioluminescent proteins such as luciferase or green fluorescent protein become an interesting protein to be studied particularly on its structure, mechanism of light emission in certain wavelength and also its contribution in several applications. This study was conducted to understand more on the luciferase enzymes from bacteria and firefly based on in silico studies of their protein sequences, protein surface and interactions with different substrates. Protein crystal structures of bacterial luciferase and firefly luciferase that been deposited on Protein Data Bank (PDB) were used as model p
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Zambito, Giorgia, Natasa Gaspar, Yanto Ridwan, et al. "Evaluating Brightness and Spectral Properties of Click Beetle and Firefly Luciferases Using Luciferin Analogues: Identification of Preferred Pairings of Luciferase and Substrate for In Vivo Bioluminescence Imaging." Molecular Imaging and Biology 22, no. 6 (2020): 1523–31. http://dx.doi.org/10.1007/s11307-020-01523-7.

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Abstract Purpose Currently, a variety of red and green beetle luciferase variants are available for bioluminescence imaging (BLI). In addition, new luciferin analogues providing longer wavelength luminescence have been developed that show promise for improved deep tissue imaging. However, a detailed assessment of these analogues (e.g., Akalumine-HCl, CycLuc1, and amino naphthyl luciferin (NH2-NpLH2)) combined with state of the art luciferases has not been performed. The aim of this study was to evaluate for the first time the in vivo brightness and spectral characteristics of firefly (Luc2), c
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Purtov, К. V., V. N. Petushkov, N. S. Rodionova, et al. "Luciferin-luciferase system of marine polychaete Chaetopterus variopedatus." Доклады Академии наук 486, no. 3 (2019): 398–402. http://dx.doi.org/10.31857/s0869-56524863398-402.

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Dissertations / Theses on the topic "Luciferine"

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Oliveira, Anderson Garbuglio de. "Estudo mecanístico da bioluminescência de fungos." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-08112010-093327/.

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Esta tese descreve como é possível obter emissão de luz in vitro enzimaticamente, a partir de extratos quente e frio de diferentes espécies de fungos bioluminescentes, o que indica também um mecanismo comum de bioluminescência em todos esses organismos. Dados cinéticos sugerem um mecanismo enzimático em duas etapas e corroboram a hipótese enzimática de Airth e Foerster, da década de 1960. Finalmente, utilizando-se extratos quente e frio foi possível também isolar a luciferina fúngica e obter sua massa molecular (298,1837 m/z). Essa substância isolada emite luz enzimaticamente in vitro, sendo q
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Chan, Wai Shing. "Applications of the bacterial luciferin-luciferase system." HKBU Institutional Repository, 2012. https://repository.hkbu.edu.hk/etd_ra/1454.

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Jathoul, Amit Paul. "Activity of firefly luciferase with 6'-amino-D-luciferin." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612384.

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Pereira, Tatiana Araujo. "Purificação e caracterização de enzimas envolvidas na bioluminescência de fungos." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-12042018-105954/.

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Esta tese descreve estudos realizados na tentativa de purificar e caracterizar enzimas envolvidas na BL de fungos, além de trabalhos conduzidos a fim de investigar o mecanismo da bioluminescência de fungos. Inicialmente, tentou-se isolar as duas enzimas supostamente responsáveis pala reação bioluminescente em fungos. Parâmetros de atividade ótima (pH e temperatura) e comportamento cinético foram investigados. Todavia, com a descoberta de que a luciferina fúngica é o derivado hidroxilado da hispidina (3-hidróxihispidina), novas estratégias foram abordadas. Os esforços se concentraram na purific
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Carvalho, Rodrigo Pimenta. "Purificação, caracterização e estudo mecanístico com luciferina fúngica." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-14092016-092016/.

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Este tese descreve métodos para a purificação e determinação da massa molecular do precursor da luciferina fúngica, a partir dos corpos de frutificação do fungo bioluminescente Neonothopanus gardneri. A molécula em questão é o substrato da primeira etapa da reação enzimática responsável pela emissão de luz em fungos, fenômeno conhecido como bioluminescência. Ao longo do projeto, foi otimizado um ensaio analítico qualitativo para detecção do precursor da luciferina em solução, e também foram desenvolvidos métodos de extração e purificação da molécula de interesse, levando sempre em consideração
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Martins, Gabriel Nobrega da Rocha. "Detecção e quantificação de derivados e intermediários de hispidina em fungos bioluminescentes e plantas por LC-MS/MS." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/46/46137/tde-24092018-160058/.

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A bioluminescência desperta o interesse humano há muitos séculos. Presente em quatro dos sete reinos taxonômicos, Monera, Chromista, Animalia e Fungi, cada um com mecanismos muito diferentes. Pode-se dizer que o estudo químico da bioluminescência começou com os experimentos de Dubois no século XIX, que cunhou os termos luciferina e luciferase, termos genéricos para o substrato e enzima envolvidos na reação, respectivamente. No caso específico de fungos, o envolvimento de enzimas foi debatido por quase cinco décadas, após a proposta enzimática de Airth e Foerster na década de 1960 e a não enzim
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Neary, A. P. "Synthesis of luciferins and related compounds." Thesis, University of Sussex, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.374484.

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Salatino, Carla Trentini. "Estudo mecanístico da reação de formação da luciferina de vaga-lume." reponame:Repositório Institucional da UFABC, 2017.

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Orientador: Prof. Dr. Luiz Francisco Monteiro Leite Ciscato<br>Dissertação (mestrado) - Universidade Federal do ABC. Programa de Pós-Graduação em Ciência e Tecnologia/Química, 2017.<br>A reação de produção de luz pelo vaga-lume envolve a oxidação enzimática da Dluciferina, um composto que contém dois anéis tiazólicos; a formação desta D-luciferina em meio biológico acontece por um processo envolvendo a reação de D-cisteína com 2-ciano-6- hidroxibenzotiazol, uma reação de mecanismo ainda desconhecido. Esta reação tem sido empregada na formação eficiente de conjugados entre duas moléculas de ati
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Rylands, Marwaan. "Syntheses of luciferins and their bioluminescent evaluation." Doctoral thesis, University of Cape Town, 2018. http://hdl.handle.net/11427/29197.

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Luciferins are a class of light emitting small molecule substrates. These molecules are oxidised to produce visible light in a reaction catalysed by the luciferase enzymes. The combination of this luminescent reaction coupled with CCD cameras, has produced revolutionary technologies that enable measurements of mammalian gene expression in cells, as well as protein-protein interactions, biochemical labelling, and small molecule flux, to name a few. Of all the luciferin molecules, D-luciferin is the most widely researched. D-Luciferin is the light emitting molecule isolated from the American fir
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Conti, Elena Eliana. "Crystal structure of firefly luciferase." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244284.

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Books on the topic "Luciferine"

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Michelin, Simone. Simone Michelin: Luciferinas. Aeroplano Editora, 2011.

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Jerome. Altercatio luciferiani et orthodoxi. Brepols Publishers, 2000.

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Karp, Matti. Applications of bacterial luciferase. M. Karp, 1988.

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Rinnekangas, Rax. Luciferin viimeinen elämä: Erään elokuvan prosessi. Like, 2013.

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Monasterios, Rubén. Rosa Luciferina y otra pieza de encaje. Producciones L. Merlano, 1988.

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Ellis, D. R. Luciferin. 1st Books Library, 2003.

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Dracko. Biblia Luciferina. Lulu Press, Inc., 2008.

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Halstead, Peter. World Luciferined. Adrian Brinkerhoff Foundation, The, 2022.

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Ford, Michael. Luciferian Goetia. Lulu Press, Inc., 2010.

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Ford, Michael. Luciferian Witchcraft. Lulu.com, 2005.

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Book chapters on the topic "Luciferine"

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Arndt, T. "Luciferin-Luciferase-System." In Lexikon der Medizinischen Laboratoriumsdiagnostik. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49054-9_1977-1.

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Arndt, T. "Luciferin-Luciferase-System." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_1977.

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Chase, Aurin M. "The Measurement of Luciferin and Luciferase." In Methods of Biochemical Analysis. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470110249.ch2.

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Brovko, L. Yu, E. Yu Cherednikova, A. Yu Chikishev, N. L. Koroteev, and N. N. Ugarova. "Light-Induced Intramolecular Dynamics in Luciferin-Luciferase Bioluminescent System." In Spectroscopy of Biological Molecules: Modern Trends. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5622-6_78.

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Windolf, J., R. Inglis, and A. Pannike. "Quantitative Bestimmung von extrazellulärem ATP nach traumatischer Gewebezerstörung mit der Luciferin-Luciferase-Reaktion." In Hefte zur Zeitschrift „Der Unfallchirurg“. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78055-4_234.

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Schomburg, Dietmar, and Dörte Stephan. "Renilla-luciferin sulfotransferase." In Enzyme Handbook. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_177.

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Niwa, Kazuki, and Dai-ichiro Kato. "Biosynthesis-Inspired Deracemizative Production of D-Luciferin In Vitro by Combining Luciferase and Thioesterase." In Bioluminescence. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2453-1_4.

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Deluca, Marlene. "Firefly Luciferase." In Advances in Enzymology - and Related Areas of Molecular Biology. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470122891.ch2.

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Schomburg, Dietmar, and Dörte Stephan. "Latia-luciferin monooxygenase (demethylating)." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_170.

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Schomburg, Dietmar, and Dörte Stephan. "Renilla-luciferin 2-monooxygenase." In Enzyme Handbook. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-57942-4_47.

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Conference papers on the topic "Luciferine"

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Prasad, Rupi. "Pros and Cons of ATP Measurement in Oil Field Waters." In CORROSION 1988. NACE International, 1988. https://doi.org/10.5006/c1988-88087.

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Abstract Measurement of bioluminescence produced by the luciferin luciferase system is a reliable method for the determination of adenosine triphosphate (ATP). In this paper the use of Luciferase ATP assay in oil field waters is evaluated and compared with the most widely used API serial dilution method. We found that the ATP method was reproducible and in close agreement with the API method when performed in laboratory conditions. ATP assay in field conditions is adversely affected by many factors. Salt concentration of water is one of the main factors that significantly reduces photometric r
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Shakhova, E. S., N. M. Myshkina, R. I. Zagitova, et al. "HETEROLOGOUS EXPRESSION OF PYROCYSTIS LUNULA LUCIFERASE GENE IN PLANT CELLS." In X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-394.

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Bioluminescence of dinoflagellates is a result of oxidation of the luciferin, which belongs to the class of tetrapyrroles and is possibly a product of chlorophyll a catabolism. We have demonstrated the functionality of the dinoflagellate luciferase gene from P. lunula in the transient and stable transformation of N. tabacum BY-2 cell culture. The results will be used further for the investigation of the luciferin biosynthetic pathway
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Marinko, Katia, Gašper Tavčar, and Marko Jeran. "The Secret of the Biochemical Reaction in the Abdomen of the Beetle: Bioluminescence of the Firefly." In Socratic Lectures 9. University of Lubljana Press, 2024. http://dx.doi.org/10.55295/psl.2024.d4.

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Abstract: Fireflies (Lampyridae) belong to a family of beetles that live widely in the humid tropical and subtropical regions of the world. They are best known for using a light organ in their abdomen to produce light, which they use to communicate with each other. Species can be distinguished by the pattern of light flickering that identifies members of a species. All larvae also glow to signal to predators that they are inedible. The light emitted by fireflies is produced by converting chemical energy into light. In this phenomenon, called bioluminescence, the substance luciferin reacts with
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Herman, A. G., and H. Bult. "RED BLOOD CELL LYSIS MAY INFLUENCE PLATELET AGGREGATION IN WHOLE BLOOD AGGREGOMETER." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644552.

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The electronic whole blood aggregometer (WBA) has the advantage that it enables the study of platelet aggregation in whole blood shortly after blood collection. Using the WBA varying results have been obtained with respect to the anti-aggregating activity of dipyridamole. As dipyridamole is an efficient inhibitor of adenosine uptake, we tested whether the degree of red blood cell lysis (and thus availability of adenine nucleotides) affected its efficacy. Citrate (10.7 mM) blood was stored in sealed tubes and used between 20 and 100 min after venipuncture. One ml was placed in a Chronolog Model
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Miyashita, Y., and M. Iwasaka. "Luciferin-luciferase bioluminescent emitting in the suspension of dia-magnetically aligned guanine microcrystals." In 2015 IEEE International Magnetics Conference (INTERMAG). IEEE, 2015. http://dx.doi.org/10.1109/intmag.2015.7157577.

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ITO, KATSUTOSHI, KAZUTO NAKAGAWA, SEIJI MURAKAMI, HIDETOSHI ARAKAWA, and MASAKO MAEDA. "DEVELOPMENT OF SIMULTANEOUS BIOLUMINESCENT ASSAY OF ACETATE KINASE AND PYRUVATE PHOSPHATE DIKINASE USING FIREFLY LUCIFERASE-LUCIFERIN REACTION." In Bioluminescence and Chemiluminescence - Progress and Current Applications - 12th International Symposium on Bioluminescence (BL) and Chemiluminescence (CL). WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776624_0102.

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Fukushima, M., T. Kataoka, N. Sugiyama, and K. Mohri. "Firefly luciferin-luciferase luminescence by milligauss ultra-low frequency pulsed magnetic field applied pure water without ATP." In INTERMAG Asia 2005: Digest of the IEEE International Magnetics Conference. IEEE, 2005. http://dx.doi.org/10.1109/intmag.2005.1464005.

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ARAKAWA, H., M. SHIOKAWA, O. IMAMURA, A. KOKADO, and M. MAEDA. "NEW BIOLUMINESCENT ASSAY OF ALKALINE PHOSPHATASE USING ADENOSINE-3'-PHOSPHATE-5'-PHOSPHOSULFATE AS SUBSTRATE AND LUCIFERIN LUCIFERASE REACTION." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0064.

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Lewis, J. C., M. J. Greene, R. G. Taylor, and R. R. Hantgan. "THROMBASTHENIC-LIKE DEFECT IN PLATELETS OF THE AFRICAN GREEN MONKEY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644557.

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African green monkeys, an animal model widely used in cardiovascular research, have platelets which ultrastructurally and functionally are similar to man. Through clinical screening of animals in a controlled breeding colony a congenital defect has been identified in platelets from an adolescent AG monkey, AJ403. The defect was characterized as abortive primary aggregation with ADP in the range 1.25-20.0 μM and PAF at concentrations to 5 × 10-6 M. Ultrastructurally, platelets within the aggregates had pseudopods, centralized granules and evidence of degranulation. Granule content release was v
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Nur, S. A., M. D. Larionova, L. P. Burakova, and E. V. Eremeeva. "THE THERMOSTABILITY ENHANCEMENT OF RENILLA MUELLERI RECOMBINANT LUCIFERASE." In X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-198.

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The use of luciferase as bioluminescent markers is often complicated by a significant decrease in enzymatic activity at physiological temperatures. To increase the thermal stability of RmY luciferase, a number of amino acid substitutions were introduced into the corresponding genetic construct by site-directed mutagenesis. The thermal stability of RmY luciferase was shown to increase in response to the introduction of selected amino acid substitutions.
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Reports on the topic "Luciferine"

1

McElroy, W. D. Firefly Luciferase-Structure and Function. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada198292.

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Wu, Anna M. F-18 Labeled Diabody-Luciferase Fusion Proteins for Optical-ImmunoPET. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1060194.

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พงษ์เลาหพันธุ์, ศุภวิวัธน์, та ธีรพงศ์ ยะทา. การพัฒนาพาหะนำส่งยีนเหนี่ยวนำการตายของเซลล์แบบอะพอพโทซิสระดับนาโน เพื่อการคุมกำเนิดสัตว์เพศผู้แบบไม่ผ่าตัดทำหมัน : ต้นแบบเพื่อการคุมจำนวนประชากรสุนัขและแมวจรจัด. คณะสัตวแพทยศาสตร์ จุฬาลงกรณ์มหาวิทยาลัย, 2019. https://doi.org/10.58837/chula.res.2019.42.

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การศึกษาวิจัยนี้มีวัตถุประสงค์ เพื่อตรวจสอบการนำไปใช้ของอนุภาคไคโตซานระดับนาโนที่ถูกดัดแปลงให้มีคุณสมบัติเป็นตัวนำส่งยีนเหนี่ยวนำการตายแบบอะพอพโทซิสเข้าสู่เซลล์อัณฑะที่มีตัวรับฮอร์โมนโกนาโดโทรปินรีลิสซิ่ง โดยการออกแบบตัวนำส่งยีนนี้สามารถนำไปใช้ประโยชน์ในการทำหมันสัตว์เพศผู้แบบไม่ผ่าตัด การศึกษานี้ได้มีการรายงานผลของอนุภาคไคโตซานระดับนาโนเชื่อมติดกับฮอร์โมนโกนาโดโทรปินรีลิสซิ่ง (Gonadotropin Releasing Hormone-modified Chitosan; GnRH-CS) เพื่อนำส่งยีนอย่างมีเป้าหมาย และการใช้เปปไทด์โกนาโดโทรปินรีลิสซิ่งในการระบุเป้าหมายการนำส่งยีนไปสู่เซลล์ที่มีตัวรับฮอร์โมนโกนาโดโทรปินรีลิสซิ่ง (GnRH receptor;
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Iglesia-Rodriguez, M. D., Oscar M. Schofield, Scott M. Glenn, and Mark Moline. Development of a Suite of Luciferase Gene Probes for the Screening and Detection of Marine Bioluminescent Systems and Organisms. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada523730.

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Iglesia-Rodriguez, M. D., Oscar M. Schofield, Scott M. Glenn, and Mark Moline. Development of a Suite of Luciferase Gene Probes for the Screening and Detection of Marine Bioluminescent Systems and Organisms. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada550656.

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Locy, Robert D., Hillel Fromm, Joe H. Cherry, and Narendra K. Singh. Regulation of Arabidopsis Glutamate Decarboxylase in Response to Heat Stress: Modulation of Enzyme Activity and Gene Expression. United States Department of Agriculture, 2001. http://dx.doi.org/10.32747/2001.7575288.bard.

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Most plants accumulate the nonprotein amino acid, g-aminobutyric acid (GABA), in response to heat stress. GABA is made from glutamate in a reaction catalyzed by glutamate decarboxylase (GAD), an enzyme that has been shown by the Israeli PI to be a calmodulin (CaM) binding protein whose activity is regulated in vitro by calcium and CaM. In Arabidopsis there are at least 5 GAD genes, two isoforms of GAD, GAD1 and GAD2, are known to be expressed, both of which appear to be calmodulin-binding proteins. The role of GABA accumulation in stress tolerance remains unclear, and thus the objectives of th
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Sessa, Guido, та Gregory Martin. MAP kinase cascades activated by SlMAPKKKε and their involvement in tomato resistance to bacterial pathogens. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7699834.bard.

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The research problem: Pseudomonas syringae pv. tomato (Pst) and Xanthomonas campestrispv. vesicatoria (Xcv) are the causal agents of tomato bacterial speck and spot diseases, respectively. These pathogens colonize the aerial parts of the plant and cause economically important losses to tomato yield worldwide. Control of speck and spot diseases by cultural practices or chemicals is not effective and genetic sources of resistance are very limited. In previous research supported by BARD, by gene expression profiling we identified signaling components involved in resistance to Xcvstrains. Follow u
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Schwartz, Bertha, Vaclav Vetvicka, Ofer Danai, and Yitzhak Hadar. Increasing the value of mushrooms as functional foods: induction of alpha and beta glucan content via novel cultivation methods. United States Department of Agriculture, 2015. http://dx.doi.org/10.32747/2015.7600033.bard.

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During the granting period, we performed the following projects: Firstly, we differentially measured glucan content in several pleurotus mushroom strains. Mushroom polysaccharides are edible polymers that have numerous reported biological functions; the most common effects are attributed to β-glucans. In recent years, it became apparent that the less abundant α-glucans also possess potent effects in various health conditions. In our first study, we explored several Pleurotus species for their total, β and α-glucan content. Pleurotuseryngii was found to have the highest total glucan concentrati
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Replenishing the malaria drug discovery pipeline: Screening and hit evaluation of the MMV Hit Generation Library 1 (HGL1) against asexual blood stage Plasmodium falciparum using a nano luciferase reporter read-out. EMBL-EBI, 2022. http://dx.doi.org/10.6019/chembl4888484.

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