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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">foodsyst</journal-id><journal-title-group><journal-title xml:lang="en">Food systems</journal-title><trans-title-group xml:lang="ru"><trans-title>Пищевые системы</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2618-9771</issn><issn pub-type="epub">2618-7272</issn><publisher><publisher-name>Федеральный научный центр пищевых систем им. В.М. Горбатова РАН</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21323/2618-9771-2019-2-1-20-22</article-id><article-id custom-type="elpub" pub-id-type="custom">foodsyst-28</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Статьи</subject></subj-group></article-categories><title-group><article-title>Features of low-temperature storage of streptomyces strains - producers of glycosidaz inhibitors</article-title><trans-title-group xml:lang="ru"><trans-title>Features of low-temperature storage of streptomyces strains - producers of glycosidaz inhibitors</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Printseva</surname><given-names>A. A.</given-names></name><name name-style="western" xml:lang="en"><surname>Printseva</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="en"><p>Anastasia A. Printseva – junior research scientist</p><p>191014, St. Petersburg, Liteyny prospect, 55</p></bio><email xlink:type="simple">djkr_yfcnz@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Sharova</surname><given-names>N. Yu/</given-names></name><name name-style="western" xml:lang="en"><surname>Sharova</surname><given-names>N. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>natalya_sharova1@mail.ru</p></bio><bio xml:lang="en"><p>Natalya Yu. Sharova – doctor of technical sciences, professor of the Russian Academy of Sciences </p><p>191014, St. Petersburg, Liteyny prospect, 55</p><p> </p></bio><email xlink:type="simple">natalya_sharova1@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Vybornova</surname><given-names>T. V.</given-names></name><name name-style="western" xml:lang="en"><surname>Vybornova</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="en"><p>Tatyana V. Vybornova – research scientist</p><p> </p><p>191014, St. Petersburg, Liteyny prospect, 55</p></bio><email xlink:type="simple">vniipakk@mail.ru</email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Manzhieva</surname><given-names>B. S.</given-names></name><name name-style="western" xml:lang="en"><surname>Manzhieva</surname><given-names>B. S.</given-names></name></name-alternatives><bio xml:lang="en"><p>Bairta S. Manzhieva – junior research scientist</p><p>191014, St. Petersburg, Liteyny prospect, 55</p></bio><email xlink:type="simple">bmanzhieva@gmail.com</email><xref ref-type="aff" rid="aff-4"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS</institution><country>Россия</country></aff><aff xml:lang="en"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS;&#13;
St. Petersburg National Research University of Information Technologies, Mechanics and Optics</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS; &#13;
St. Petersburg National Research University of Information Technologies, Mechanics and Optics</institution><country>Россия</country></aff><aff xml:lang="en"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS; &#13;
St. Petersburg National Research University of Information Technologies, Mechanics and Optics</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS; &#13;
St. Petersburg National Research University of Information Technologies, Mechanics and Optics</institution><country>Россия</country></aff><aff xml:lang="en"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS</institution><country>Россия</country></aff><aff xml:lang="en"><institution>All-Russian Research Institute for Food Additives – Branch of V.M. Gorbatov Federal Research Center for Food Systems of RAS</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>17</day><month>04</month><year>2019</year></pub-date><volume>2</volume><issue>1</issue><fpage>20</fpage><lpage>22</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Printseva A.A., Sharova N.Y., Vybornova T.V., Manzhieva B.S., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Printseva A.A., Sharova N.Y., Vybornova T.V., Manzhieva B.S.</copyright-holder><copyright-holder xml:lang="en">Printseva A.A., Sharova N.Y., Vybornova T.V., Manzhieva B.S.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.fsjour.com/jour/article/view/28">https://www.fsjour.com/jour/article/view/28</self-uri><abstract><p>The aim of the work is to study the inhibitory activity of the Streptomyces lucensis VKPM Ac-1743 and Streptomyces violaceus VKPM Ac-1734 strains stored at –18 °C in a 15 % glycerol solution and in a 0.9 % sodium chloride solution.</p><p>The object of the study was the actinomycete strains of S. lucensis VKPM Ac-1743 and S. violaceus VKPM Ac-1734 producers of glycosidase inhibitor, which is a micro-ingredient for creating products with a low glycemic index. The storage time was nine months. Bookmark storage was performed by flushing with a taped agar starchcontaining environment of Capek. For comparison, we studied the properties of cultures stored at +4 °C without cryoprotectant.</p><p>Deep cultivation of Streptomyces strains was carried out in a periodic manner on a medium containing corn starch hydrolyzate under the Multitron incubator shaker (INFORS,Switzerland).</p><p>Inhibitory activity was determined in inactivated native solutions by a colorimetric method with respect to pancreatic α-amylase, a test glycosidase involved in carbohydrate metabolism, and whose activity was chosen as a criterion for assessing the hypoglycemic action of the inhibitor. The proteinase activity of the inactivated native solution was determined by a modified method using a casein substrate.</p><p>The experimental data were processed using the methods of mathematical statistics and Excel XP programs.</p><p>As a result of the research, it was established that the actinomycete strains of S. lucensis and S. violaceus, the producers of glycosidase inhibitors, can maintain inhibitory activity during low-temperature storage for nine months.</p><p>For the S. lucensis actinomycete strain, stored in a 15 % glycerol solution at – 18 °C, the maximum inhibitory activity is 48 hours in the biotechnological process and is (3686 ± 300) IU/cm3 native solution, and for the violaceus strain – (3150 ± 200) IU/cm³ of the native solution, respectively.</p><p>For the strain of actinomycete S. lucensis, stored in 0.9 % sodium chloride solution at a temperature of – 18 °C, the maximum inhibitory activity accounts for 72 h of the biotechnological process and is (2600 ± 200) IU/cm³ of the native solution, and for the strain S. violaceus the maximum inhibitory activity accounts for 24 hours of the biotechnological process and is (3530 ± 200) IU/cm³ of the native solution.</p><p>At a storage temperature of +4 °C, the inhibitory activity for the strain of actinomycete S. lucensis is (560 ± 20) IU/cm³ of native solution, and for the strain of S. violaceus – (1747 ± 100) IU/cm³ of native solution, respectively. On the basis of the data obtained, it can be concluded that a temperature of –18 °C is preferred for long-term storage.</p><p>During the cultivation of Streptomyces strains, proteinase activity ranged from (0,012 ± 0,001) U/cm³ to (0,072 ± 0,002) U/cm³.</p><p>The obtained data can be applied in further studies to develop conditions for long-term storage of collection crops.</p></abstract><trans-abstract xml:lang="ru"><p>The aim of the work is to study the inhibitory activity of the Streptomyces lucensis VKPM Ac-1743 and Streptomyces violaceus VKPM Ac-1734 strains stored at –18 °C in a 15 % glycerol solution and in a 0.9 % sodium chloride solution.</p><p>The object of the study was the actinomycete strains of S. lucensis VKPM Ac-1743 and S. violaceus VKPM Ac-1734 producers of glycosidase inhibitor, which is a micro-ingredient for creating products with a low glycemic index. The storage time was nine months. Bookmark storage was performed by flushing with a taped agar starchcontaining environment of Capek. For comparison, we studied the properties of cultures stored at +4 °C without cryoprotectant.</p><p>Deep cultivation of Streptomyces strains was carried out in a periodic manner on a medium containing corn starch hydrolyzate under the Multitron incubator shaker (INFORS,Switzerland).</p><p>Inhibitory activity was determined in inactivated native solutions by a colorimetric method with respect to pancreatic α-amylase, a test glycosidase involved in carbohydrate metabolism, and whose activity was chosen as a criterion for assessing the hypoglycemic action of the inhibitor. The proteinase activity of the inactivated native solution was determined by a modified method using a casein substrate.</p><p>The experimental data were processed using the methods of mathematical statistics and Excel XP programs.</p><p>As a result of the research, it was established that the actinomycete strains of S. lucensis and S. violaceus, the producers of glycosidase inhibitors, can maintain inhibitory activity during low-temperature storage for nine months.</p><p>For the S. lucensis actinomycete strain, stored in a 15 % glycerol solution at – 18 °C, the maximum inhibitory activity is 48 hours in the biotechnological process and is (3686 ± 300) IU/cm3 native solution, and for the violaceus strain – (3150 ± 200) IU/cm³ of the native solution, respectively.</p><p>For the strain of actinomycete S. lucensis, stored in 0.9 % sodium chloride solution at a temperature of – 18 °C, the maximum inhibitory activity accounts for 72 h of the biotechnological process and is (2600 ± 200) IU/cm³ of the native solution, and for the strain S. violaceus the maximum inhibitory activity accounts for 24 hours of the biotechnological process and is (3530 ± 200) IU/cm³ of the native solution.</p><p>At a storage temperature of +4 °C, the inhibitory activity for the strain of actinomycete S. lucensis is (560 ± 20) IU/cm³ of native solution, and for the strain of S. violaceus – (1747 ± 100) IU/cm³ of native solution, respectively. On the basis of the data obtained, it can be concluded that a temperature of –18 °C is preferred for long-term storage.</p><p>During the cultivation of Streptomyces strains, proteinase activity ranged from (0,012 ± 0,001) U/cm³ to (0,072 ± 0,002) U/cm³.</p><p>The obtained data can be applied in further studies to develop conditions for long-term storage of collection crops.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>strain of Streptomyces lucensis VKPM Ас-1743</kwd><kwd>strain of Streptomyces violaceus VKPM Ас-1734</kwd><kwd>low-temperature storage</kwd><kwd>inhibitory activity</kwd><kwd>proteinase activity</kwd></kwd-group><kwd-group xml:lang="en"><kwd>strain of Streptomyces lucensis VKPM Ас-1743</kwd><kwd>strain of Streptomyces violaceus VKPM Ас-1734</kwd><kwd>low-temperature storage</kwd><kwd>inhibitory activity</kwd><kwd>proteinase activity</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Pokhilenko, V.D., Baranov, A.M., Detushev, K.V. 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