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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Food Processing: Techniques and Technology</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Food Processing: Techniques and Technology</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>Техника и технология пищевых производств</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">2074-9414</issn>
   <issn publication-format="online">2313-1748</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">6a84bb6894fbba14f785cf9d</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>НАУЧНАЯ СТАТЬЯ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>RESEARCH ARTICLE</subject>
    </subj-group>
    <subj-group>
     <subject>НАУЧНАЯ СТАТЬЯ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">EXPERIENCE OF THE DEPARTMENT OF «BIONANOTECHNOLOGY» OF THE KEMEROVO INSTITUTE OF FOOD SCIENCE AND TECHNOLOGY IN THE FIELD OF BIOTECHNOLOGY OF OBTAINING RECOMBINANT ENZYME PREPARATIONS</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>ОПЫТ КАФЕДРЫ «БИОНАНОТЕХНОЛОГИЯ» КЕМЕРОВСКОГО ТЕХНОЛОГИЧЕСКОГО ИНСТИТУТА ПИЩЕВОЙ ПРОМЫШЛЕННОСТИ В ОБЛАСТИ БИОТЕХНОЛОГИИ ПОЛУЧЕНИЯ РЕКОМБИНАНТНЫХ ФЕРМЕНТНЫХ ПРЕПАРАТОВ</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5630-3196</contrib-id>
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Просеков</surname>
       <given-names>Александр Юрьевич</given-names>
      </name>
      <name xml:lang="en">
       <surname>Prosekov</surname>
       <given-names>Alexander Yu.</given-names>
      </name>
     </name-alternatives>
     <bio xml:lang="ru">
      <p>доктор технических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of technical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
    <contrib contrib-type="author">
     <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4921-8997</contrib-id>
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Бабич</surname>
       <given-names>Ольга Олеговна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Babich</surname>
       <given-names>Olga O.</given-names>
      </name>
     </name-alternatives>
     <email>OOBabich@kantiana.ru</email>
     <bio xml:lang="ru">
      <p>доктор технических наук;</p>
     </bio>
     <bio xml:lang="en">
      <p>doctor of technical sciences;</p>
     </bio>
     <xref ref-type="aff" rid="aff-2"/>
    </contrib>
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Солдатова</surname>
       <given-names>Любовь Сергеевна</given-names>
      </name>
      <name xml:lang="en">
       <surname>Soldatova</surname>
       <given-names>L. S.</given-names>
      </name>
     </name-alternatives>
     <xref ref-type="aff" rid="aff-3"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Кемеровский государственный университет</institution>
     <city>Кемерово</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Kemerovo State University</institution>
     <city>Kemerovo</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-2">
    <aff>
     <institution xml:lang="ru">ФГАОУ ВО «Балтийский федеральный университет имени Иммануила Канта»</institution>
     <city>Калининград</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Immanuel Kant Baltic Federal University</institution>
     <city>Kaliningrad</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <aff-alternatives id="aff-3">
    <aff>
     <institution xml:lang="ru">ФГБОУ ВПО «Кемеровский технологический институт  пищевой промышленности»</institution>
     <city>Кемерово</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Kemerovo Institute of Food Science and Technology</institution>
     <city>Kemerovo</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <fpage>102</fpage>
   <lpage>111</lpage>
   <permissions>
    <copyright-statement xml:lang="ru">© Просеков А.Ю., Бабич О.О., Солдатова Л.С.</copyright-statement>
    <copyright-statement xml:lang="en">© Prosekov A.Y., Babich O.O., Soldatova L.S.</copyright-statement>
    <copyright-holder xml:lang="ru">Просеков Александр Юрьевич, Бабич Ольга Олеговна, Солдатова Любовь Сергеевна</copyright-holder>
    <copyright-holder xml:lang="en">Prosekov Alexander Yu., Babich Olga O., Soldatova L. S.</copyright-holder>
   </permissions>
   <self-uri xlink:href="https://jsocnet.ru/en/nauka/publications/6a84bb6894fbba14f785cf9d/view">https://jsocnet.ru/en/nauka/publications/6a84bb6894fbba14f785cf9d/view</self-uri>
   <abstract xml:lang="ru">
    <p>Проведен обзор современных методов получения рекомбинантных ферментов для пищевой промышлен-ности. Подобраны оптимальные условия получения рекомбинантной L-фенилаланин-аммоний-лиазы Rhodosporidium toruloides, выделенной из Escherichia coli. Доля целевого белка, полученного после индукции, составила 40 % суммарного белка клетки. Проведена очистка полученного белка на Ni-NTA агарозе. Степень очистки белка составила более 90 %.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>The review of modern methods of obtaining recombinant enzymes for food industry is given. Optimum condi-tions to obtain recombinant L-phenylalanine-ammonia-lyase Rhodosporidium toruloides allocated from Escherichia coli have been established. The share of the special-purpose protein obtained after the induction was 40 % of the total cell protein. The clearing of the obtained protein on Ni-NTA agarose has been done. The degree of protein clearing was more than 90 %.</p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>Рекомбинантный штамм</kwd>
    <kwd>фермент</kwd>
    <kwd>клонирование</kwd>
    <kwd>генетическая инженерия</kwd>
    <kwd>конструирование</kwd>
    <kwd>L-фенилаланин-аммоний-лиаза</kwd>
    <kwd>трансформация</kwd>
    <kwd>вектор экспрессии.</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>Recombinant strain</kwd>
    <kwd>enzyme</kwd>
    <kwd>cloning</kwd>
    <kwd>genetic engineering</kwd>
    <kwd>construction</kwd>
    <kwd>L-phenylalanine-ammonia-lyase</kwd>
    <kwd>trans-formation</kwd>
    <kwd>expression vector.</kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <p></p>
 </body>
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