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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="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">catal</journal-id><journal-title-group><journal-title xml:lang="ru">Катализ в промышленности</journal-title><trans-title-group xml:lang="en"><trans-title>Kataliz v promyshlennosti</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1816-0387</issn><issn pub-type="epub">2413-6476</issn><publisher><publisher-name>LLC "KALVIS"</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">catal-231</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>БИОКАТАЛИЗ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>BIOCATALYSIS</subject></subj-group></article-categories><title-group><article-title>БИОКАТАЛИТИЧЕСКИЕ ГЕТЕРОГЕННЫЕ ПРОЦЕССЫ ПЕРЕЭТЕРИФИКАЦИИ РАСТИТЕЛЬНЫХ МАСЕЛ В БИОДИЗЕЛЬ</article-title><trans-title-group xml:lang="en"><trans-title>BIOCATALYTIC HETEROGENEOUS PROCESSES OF INTERESTERIFICATION OF VEGETABLE OILS INTO BIODIESEL</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>Коваленко</surname><given-names>Г. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kovalenko</surname><given-names>G. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д-р хим. наук, проф., ведущий науч. сотрудник Института катализа СО РАН, руководитель группы биокатализа. Тел.: (383) 326-97-43</p></bio><email xlink:type="simple">galina@catalysis.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>Перминова</surname><given-names>Л. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Perminova</surname><given-names>L. V.</given-names></name></name-alternatives><bio xml:lang="ru"/><email xlink:type="simple">perminova@catalysis.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>Беклемишев</surname><given-names>А. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Beklemishev</surname><given-names>A. B.</given-names></name></name-alternatives><bio xml:lang="ru"/><email xlink:type="simple">beklem@soramn.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>Яковлева</surname><given-names>Е. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Yakovleva</surname><given-names>E. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. хим. наук, ст. науч. сотрудник Института катализа СО РАН. Тел.: (383) 326-97-69</p></bio><email xlink:type="simple">yakovl@catalysis.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>Пыхтина</surname><given-names>М. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Pykhtina</surname><given-names>M. B.</given-names></name></name-alternatives><bio xml:lang="ru"/><email xlink:type="simple">oganer87@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Институт катализа им. Г.К. Борескова СО РАН, г. Новосибирск</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>Институт биохимии СО РАМН, г. Новосибирск</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2014</year></pub-date><pub-date pub-type="epub"><day>21</day><month>07</month><year>2015</year></pub-date><volume>0</volume><issue>6</issue><fpage>71</fpage><lpage>79</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; LLC "KALVIS", 2015</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="ru">LLC "KALVIS"</copyright-holder><copyright-holder xml:lang="en">LLC "KALVIS"</copyright-holder><license xlink:href="https://www.catalysis-kalvis.ru/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.catalysis-kalvis.ru/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.catalysis-kalvis.ru/jour/article/view/231">https://www.catalysis-kalvis.ru/jour/article/view/231</self-uri><abstract><p>Проведены исследования гетерогенного биокаталитического процесса переэтерификации растительных масел в этиловые эфиры жирных кислот с участием этанола или этилацетата и биокатализаторов, приготовленных путем включения в ксерогель диоксида кремния клеточных лизатов рекомбинантного штамма rE.сoli/lip, продуцирующего термостабильную липазу из Thermo-myces lanuginosus. Процесс переэтерификации растительного масла проводили как в периодическом режиме в реакторе смешения, так и в непрерывном режиме в реакторе с неподвижным слоем приготовленного биокатализатора. Показано, что этил-ацетат является оптимальным ацилирующим реагентом в ре-акции переэтрификации триглицеридов растительного масла в этиловые эфиры жирных кислот. В отличие от этанола этот реагент не инактивирует биокатализатор необратимо. Время полуинактивации биокатализаторов в изученных условиях составило 720 ч при 40 °С. </p></abstract><trans-abstract xml:lang="en"><p>Heterogeneous biocatalytic transesterification of vegetable oils into ethyl esters of fatty acids was studied. The process was carried out with ethanol or ethyl acetate and biocatalysts prepared by entrapping in silica xerogel of cell lysate of the recombinant strain rE.сoli/lip, that produces thermostable lipase from Thermomyces la-nuginosus. The transesterification of vegetable oil was performed both in a periodic mode in a stirred tank reactor and in a continuous mode in a fixed bed reactor. It was shown that ethyl acetate is an optimal acylating reagent for the interesterification of vegetable oil triglycerides into fatty acid ethyl esters. Unlike ethanol, this reagent does not inactivates biocatalyst irreversibly. The period of semi-inactivation of the biocatalysts was 720 h at 40 °C. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>гетерогенные биокатализаторы</kwd><kwd>лизаты рекомбинантного штамма-продуцента термостабильной липазы</kwd><kwd>включение в ксерогель диоксида кремния</kwd><kwd>переэтерификация растительного масла этилацетатом</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Heterogeneous biocatalysts</kwd><kwd>Lysates of recombinant strain-producer of thermostable lipase</kwd><kwd>Entrapment inside silica xerogel</kwd><kwd>Interesterification of vegetable oils by ethyl acetate</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">Росс М.Ю., Стребков Д.С. Биодизельное топливо из водо-рослей. М., 2008. С. 88—162.</mixed-citation><mixed-citation xml:lang="en">Росс М.Ю., Стребков Д.С. Биодизельное топливо из водо-рослей. М., 2008. 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