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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">10679</article-id><article-id pub-id-type="doi">10.32607/20758251-2011-3-2-79-89</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>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">Reconstruction of Purine Metabolism in Bacillus subtilis to Obtain the Strain Producer of AICAR: A New Drug with a Wide Range of Therapeutic Applications</article-title><trans-title-group xml:lang="ru"><trans-title>Reconstruction of Purine Metabolism in Bacillus subtilis to Obtain the Strain Producer of AICAR: A New Drug with a Wide Range of Therapeutic Applications</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>Lobanov</surname><given-names>K V</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Errais Lopes</surname><given-names>L</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Korol'kova</surname><given-names>N V</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Tyaglov</surname><given-names>B V</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Glazunov</surname><given-names>A V</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Shakulov</surname><given-names>R S</given-names></name><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Mironov</surname><given-names>A S</given-names></name><email>alexmir@genetika.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">State Research Institute for Genetics and Selection of Industrial Microorganisms</institution></aff><aff><institution xml:lang="ru"></institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2011-06-15" publication-format="electronic"><day>15</day><month>06</month><year>2011</year></pub-date><volume>3</volume><issue>2</issue><issue-title xml:lang="en">VOL 3, NO2 (2011)</issue-title><issue-title xml:lang="ru">ТОМ 3, №2 (2011)</issue-title><fpage>79</fpage><lpage>89</lpage><history><date date-type="received" iso-8601-date="2020-01-17"><day>17</day><month>01</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2011, Lobanov K.V., Errais Lopes L., Korol'kova N.V., Tyaglov B.V., Glazunov A.V., Shakulov R.S., Mironov A.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2011, Lobanov K.V., Errais Lopes L., Korol'kova N.V., Tyaglov B.V., Glazunov A.V., Shakulov R.S., Mironov A.S.</copyright-statement><copyright-year>2011</copyright-year><copyright-holder xml:lang="en">Lobanov K.V., Errais Lopes L., Korol'kova N.V., Tyaglov B.V., Glazunov A.V., Shakulov R.S., Mironov A.S.</copyright-holder><copyright-holder xml:lang="ru">Lobanov K.V., Errais Lopes L., Korol'kova N.V., Tyaglov B.V., Glazunov A.V., Shakulov R.S., Mironov A.S.</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/10679">https://actanaturae.ru/2075-8251/article/view/10679</self-uri><abstract xml:lang="en"><p/></abstract><trans-abstract xml:lang="ru"><p>AICAR is a natural compound, an analogue and precursor of adenosine. As activator of AMP-activated protein kinase (AMPK), AICAR has a broad therapeutic potential, since it normalizes the carbohydrate and lipid metabolism and inhibits the proliferation of tumor cells. The synthesis of AICAR in Bacillus subtilis cells is controlled by the enzymes of purine biosynthesis; their genes constituting purine operon (pur-operon). Reconstruction of purine metabolism in B. subtilis was performed to achieve overproduction of AICAR. For this purpose, the gene purH, which encodes formyltransferase/IMP-cyclohydrolase, an enzyme that controls the conversion of AICAR to IMP, was removed from the B. subtilis genome, ensuring the accumulation of AICAR. An insertion inactivating the gene purR that encodes the negative transcriptional regulator of the purine biosynthesis operon was introduced into the B.subtilis chromosome in order to boost the production of AICAR; the transcription attenuator located in the leader sequence of pur-operon was deleted. Furthermore, the expression integrative vector carrying a strong promoter of the rpsF gene encoding the ribosomal protein S6 was designed. The heterologous Escherichia coli gene purF encoding the first enzyme of the biosynthesis of purines with impaired allosteric regulation, as well as the modified E.coli gene prs responsible for the synthesis of the precursor of purines - phosphoribosyl pyrophosphate (PRPP) - was cloned into this vector under the control of the rpsF gene promoter. The modified purF and prs genes were inserted into the chromosome of the B. subtilis strain. B. subtilis strain obtained by these genetic manipulations accumulates 11-13 g/L of AICAR in the culture fluid.</p></trans-abstract><kwd-group xml:lang="en"><kwd>anticancer agent AICAR</kwd><kwd>purine metabolism</kwd><kwd>genome reconstruction</kwd><kwd>Bacillus subtilis strain - producer of AICAR</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Buchanan J.M., Hartman S.C. // Adv. Enzymol. Relat. Areas Mol. Biol. 1959. V. 21. P. 199-261.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Zalkin H., Nygaard P. // Escherichia coli and Salmonella. Washington, Dc.: ASM Press, 1996. P. 561-579.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Switzer R.L., Zalkin H., Saxild H.H. // Bacillus subtilis and its closest relatives: from genes to cells. Washington, Dc.: ASM Press, 2002. 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