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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Acta Naturae</journal-id><journal-title-group><journal-title xml:lang="en">Acta Naturae</journal-title><trans-title-group xml:lang="ru"><trans-title>Acta Naturae</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-8251</issn><publisher><publisher-name xml:lang="en">Acta Naturae Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">27315</article-id><article-id pub-id-type="doi">10.32607/actanaturae.27315</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Research Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Экспериментальные статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en"><italic>Streptomyces phaeochromogenes</italic> BV-204, K-1115А Anthraquinone-Producing Strain: A New Protein Biosynthesis Inhibitor</article-title><trans-title-group xml:lang="ru"><trans-title><italic>Streptomyces phaeochromogenes</italic> БВ-204 – штамм-продуцент антрахинона К-1115А, нового ингибитора биосинтеза белка</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Belik</surname><given-names>A. R.</given-names></name><name xml:lang="ru"><surname>Белик</surname><given-names>А. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>metrim@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zakalyukina</surname><given-names>Yu. V.</given-names></name><name xml:lang="ru"><surname>Закалюкина</surname><given-names>Ю. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>juline@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Alferova</surname><given-names>V. A.</given-names></name><name xml:lang="ru"><surname>Алферова</surname><given-names>В. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>metrim@gmail.com</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Buyuklyan</surname><given-names>Y. A.</given-names></name><name xml:lang="ru"><surname>Буюклян</surname><given-names>Ю. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>metrim@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Osterman</surname><given-names>I. A.</given-names></name><name xml:lang="ru"><surname>Остерман</surname><given-names>И. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>metrim@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Biryukov</surname><given-names>M. V.</given-names></name><name xml:lang="ru"><surname>Бирюков</surname><given-names>М. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>metrim@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Sirius University of Science and Technology</institution></aff><aff><institution xml:lang="ru">Научно-технологический университет «Сириус»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Lomonosov Moscow State University</institution></aff><aff><institution xml:lang="ru">Московский государственный университет имени М.В. Ломоносова</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry</institution></aff><aff><institution xml:lang="ru">Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова РАН</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Skolkovo Institute of Science and Technology</institution></aff><aff><institution xml:lang="ru">Сколковский институт науки и технологий</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2024-05-10" publication-format="electronic"><day>10</day><month>05</month><year>2024</year></pub-date><volume>16</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>30</fpage><lpage>39</lpage><history><date date-type="received" iso-8601-date="2023-11-02"><day>02</day><month>11</month><year>2023</year></date><date date-type="accepted" iso-8601-date="2024-01-24"><day>24</day><month>01</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Belik A.R., Zakalyukina Y.V., Alferova V.A., Buyuklyan Y.A., Osterman I.A., Biryukov M.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Белик А.Р., Закалюкина Ю.В., Алферова В.А., Буюклян Ю.А., Остерман И.А., Бирюков М.В.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Belik A.R., Zakalyukina Y.V., Alferova V.A., Buyuklyan Y.A., Osterman I.A., Biryukov M.V.</copyright-holder><copyright-holder xml:lang="ru">Белик А.Р., Закалюкина Ю.В., Алферова В.А., Буюклян Ю.А., Остерман И.А., Бирюков М.В.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://actanaturae.ru/2075-8251/article/view/27315">https://actanaturae.ru/2075-8251/article/view/27315</self-uri><abstract xml:lang="en"><p>In the search for new antibiotics, it is a common occurrence that already known molecules are “rediscovered” while new promising ones remain unnoticed. A possible solution to this problem may be the so-called “target-oriented” search, using special reporter microorganisms that combine increased antibiotic sensitivity with the ability to identify a molecule’s damaging effect. The use of such test organisms makes it possible to discover new promising properties even in known metabolites. In this study, we used a high-throughput screening method based on the pDualrep2 dual reporter system, which combines high sensitivity through the use of modified strains of test organisms and makes it possible to easily and accurately identify the interaction mechanisms of a substance and a bacterial cell at the initial stages of screening. This reporter system is unknown in Russia and is significantly superior to its global analogues. In the system, translation inhibition induces the expression of the fluorescent protein Katushka2s, while DNA damage is induced by TurboRFP. Using pDualrep2, we have isolated and described BV-204, an <italic>S. phaeochromogenes</italic> strain producing K-1115A, the biologically active substance that we have previously described. In our study, K-1115A for the first time has demonstrated antibiotic activity and an ability to inhibit bacterial translation, which was confirmed in vitro in a cell-free translation system for FLuc mRNA. K-1115A’s antibacterial activity was tested and confirmed for S. aureus (MRSA) and B. subtilis, its cytotoxicity measured against that for the HEK293 cell line. Its therapeutic index amounted to 2 and 8, respectively. The obtained results open up prospects for further study of K-1115A; so, this can be regarded as the basis for the production of semi-synthetic derivatives with improved therapeutic properties to be manufactured in dosage forms.</p></abstract><trans-abstract xml:lang="ru"><p>Важной проблемой при поиске новых антибиотиков является «переоткрытие», то есть обнаружение уже известных молекул и тот факт, что на их фоне могут теряться новые молекулы с перспективными механизмами действия. Возможным решением этой проблемы может быть так называемый мишень-ориентированный поиск с использованием специальных репортерных микроорганизмов, сочетающих повышенную антибиотикочувствительность со способностью демонстрировать характер повреждающего действия изучаемых молекул. Использование подобных тест-организмов позволяет обнаружить новые интересные свойства даже у известных метаболитов. В данном исследовании использован метод высокопроизводительного скрининга на основе двойной репортерной системы pDualrep2, высокая чувствительность которой, обусловленная использованием модифицированных штаммов тест-организмов, сочетается с возможностью легко и точно выявлять механизмы взаимодействия вещества с бактериальной клеткой на первичных этапах скрининга. Эта репортерная система не имеет аналогов в России и существенно превосходит мировые аналоги. Ингибирование трансляции индуцирует экспрессию флуоресцентного белка Katushka2s, а повреждение ДНК – TurboRFP. При помощи pDualrep2 нами выделен и описан штамм <italic>Streptomyces phaeochromogenes</italic> БВ-204, продуцент описанного ранее биологически активного вещества К-1115А, антибиотическая активность которого и способность ингибировать бактериальную трансляцию впервые были продемонстрированы в нашей работе. Этот эффект подтвержден нами в in vitro системе бесклеточной трансляции мРНК FLuc. Антибактериальная активность вещества К-1115А проверена и подтверждена на клетках S. aureus (MRSA) и B. subtilis, а также сопоставлена с цитотоксичностью на клеточной линии HEK293. Определен терапевтический индекс данного соединения, составивший 2 и 8 соответственно. Полученные результаты и описанные нами новые свойства К-1115А открывают перспективы его дальнейшего изучения и позволяют рассматривать данное соединение как основу для получения полусинтетических производных с улучшенными терапевтическими свойствами и разработки в дальнейшем лекарственных форм.</p></trans-abstract><kwd-group xml:lang="en"><kwd>actinomycetes</kwd><kwd>K-1115A</kwd><kwd>antibiotics</kwd><kwd>reporter system pDualrep2</kwd><kwd>inhibition of protein biosynthesis</kwd><kwd>in vitro translation</kwd><kwd>citizen science</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>актиномицеты</kwd><kwd>К-1115А</kwd><kwd>антибиотики</kwd><kwd>репортерная система pDualrep2</kwd><kwd>ингибирование биосинтеза белка</kwd><kwd>in vitro трансляция</kwd><kwd>«гражданская наука»</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">Министерство науки и высшего образования Российской Федерации</institution></institution-wrap><institution-wrap><institution xml:lang="en">Ministry of Science and Higher Education of the Russian Federation</institution></institution-wrap></funding-source><award-id>075-10-2021-093</award-id></award-group></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Abdel-Razek A.S., El-Naggar M.E., Allam A., Morsy O.M., Othman S.I. // Processes. 2020. 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