<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">antibiotics</journal-id><journal-title-group><journal-title xml:lang="ru">Антибиотики и Химиотерапия</journal-title><trans-title-group xml:lang="en"><trans-title>Antibiot Khimioter = Antibiotics and Chemotherapy</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0235-2990</issn><publisher><publisher-name>ООО «Издательство ОКИ»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">antibiotics-687</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>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Вторичные метаболиты морских микроорганизмов. II. Морские грибы и места их обитания</article-title><trans-title-group xml:lang="en"><trans-title>Secondary Metabolites from Marine Microorganisms. II. Marine Fungi and Their Habitats</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>Орлова</surname><given-names>Т. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Orlova</surname><given-names>T. I.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Булгакова</surname><given-names>В. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Bulgakova</surname><given-names>V. G.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Полин</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Polin</surname><given-names>A. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Московский государственный университет им. М. В. Ломоносова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>M. V. Lomonosov Moscow State University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>13</day><month>05</month><year>2020</year></pub-date><volume>61</volume><issue>9-10</issue><fpage>52</fpage><lpage>63</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; ООО «Издательство ОКИ», 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">ООО «Издательство ОКИ»</copyright-holder><copyright-holder xml:lang="en">ООО «Издательство ОКИ»</copyright-holder><license xlink:href="https://www.antibiotics-chemotherapy.ru/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.antibiotics-chemotherapy.ru/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.antibiotics-chemotherapy.ru/jour/article/view/687">https://www.antibiotics-chemotherapy.ru/jour/article/view/687</self-uri><abstract><p>Морские грибы представляют большой интерес, как новый многообещающий источник биологически активных веществ - противоопухолевых соединений, антибиотиков, ингибиторов биохимических процессов. Поскольку морские организмы обитают в биологически конкурентной среде с уникальными условиями, вторичные метаболиты морских грибов отличаются значительным многообразием. Последние исследования в области генома показали, что грибы могут быть носителями генных кластеров, кодирующих образование ранее неизвестных вторичных метаболитов. Активизация таких ослабленных или спящих генов может быть использована как для повышения активности известных соединений, так и для выделения новых веществ.</p></abstract><trans-abstract xml:lang="en"><p>Marine-derived fungi are of great interest as a new promising source of biologically active products such as anticancer compounds, antibiotics, inhibitors of biochemical processes. Since marine organisms inhabit biologically competitive environment with unique conditions, the chemical diversity of the secondary metabolites from marine fungi is considerably high. Recent genomic studies demonstrated that fungi can carry gene clasters encoding production of previously unknown secondary metabolites. Activation of the attenuated or silent genes would be useful either for improving activities of the known compounds or for discovery of new products.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>морские грибы</kwd><kwd>биоактивные вторичные метаболиты</kwd><kwd>активизация спящих генов биосинтеза</kwd><kwd>глубоководные гидротермальные выбросы (чёрные курильщики)</kwd><kwd>солеустойчивые грибы</kwd><kwd>экстримофильные грибы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>marine fungi</kwd><kwd>bioactive secondary metabolites</kwd><kwd>activation of silent biosynthetic genes</kwd><kwd>deep-sea hydrothermal vents</kwd><kwd>halotolerant fungi</kwd><kwd>extremophilic fungi</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">Dyshlovoy S.A., Honecker F. Marine compounds and cancer: Where do we stand? Mar Drugs 2015; 13: 5657-5665.</mixed-citation><mixed-citation xml:lang="en">Dyshlovoy S.A., Honecker F. Marine compounds and cancer: Where do we stand? Mar Drugs 2015; 13: 5657-5665.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng L-N, Wang Y-J, Sheng J. et al. Antitumor peptides from marine organisms. Mar Drugs 2011; 9: 1840-1859.</mixed-citation><mixed-citation xml:lang="en">Zheng L-N, Wang Y-J, Sheng J. et al. Antitumor peptides from marine organisms. Mar Drugs 2011; 9: 1840-1859.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Stonic V.A., Fedorow S. Marine low molecular weight natural products as potential cancer preventive compounds.Mar Drugs 2014; 12: 2: 636-671.</mixed-citation><mixed-citation xml:lang="en">Stonic V.A., Fedorow S. Marine low molecular weight natural products as potential cancer preventive compounds.Mar Drugs 2014; 12: 2: 636-671.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Fouilaud M., Venkatachlam M., Girand-Valenciennes E. et al. Antraquinone and derivatives from marine-derived fungi: structural diversity and selected biological activities. Mar Drugs 2016; 14: 4: pii E64</mixed-citation><mixed-citation xml:lang="en">Fouilaud M., Venkatachlam M., Girand-Valenciennes E. et al. Antraquinone and derivatives from marine-derived fungi: structural diversity and selected biological activities. Mar Drugs 2016; 14: 4: pii E64</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Blunt J.W., Copp B.R., Keyzers R.A. et al. Marine natural products. Nat Prod Rep 2016; 33: 3: 382-431.</mixed-citation><mixed-citation xml:lang="en">Blunt J.W., Copp B.R., Keyzers R.A. et al. Marine natural products. Nat Prod Rep 2016; 33: 3: 382-431.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Imhoff J. Natural products from marine fungi - still an underrepresented resourse. Mar Drugs 2016; 14: 1: 19.</mixed-citation><mixed-citation xml:lang="en">Imhoff J. Natural products from marine fungi - still an underrepresented resourse. Mar Drugs 2016; 14: 1: 19.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Kjer J., Debbab A., Aly A.N., Proksch P. Methods for isolation of marine-derived endophytic fungi and their bioactive secondary products. Nat Protoc 2010; 5: 3: 479-490.</mixed-citation><mixed-citation xml:lang="en">Kjer J., Debbab A., Aly A.N., Proksch P. Methods for isolation of marine-derived endophytic fungi and their bioactive secondary products. Nat Protoc 2010; 5: 3: 479-490.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Xiong Z-Q., Wang J-F., Hao Y-Y., Wang Y. Recent advances in the discovery and development of marine microbial products. Mar Drugs 2013; 11: 3: 700-717.</mixed-citation><mixed-citation xml:lang="en">Xiong Z-Q., Wang J-F., Hao Y-Y., Wang Y. Recent advances in the discovery and development of marine microbial products. Mar Drugs 2013; 11: 3: 700-717.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Reen F.J., Romano S., Dobson A.D., O'Gara. The sound of silence: activating silent biosynthetic gene clasters in marine microorganisms. Mar Drugs 2015; 13: 8: 4754-4783.</mixed-citation><mixed-citation xml:lang="en">Reen F.J., Romano S., Dobson A.D., O'Gara. The sound of silence: activating silent biosynthetic gene clasters in marine microorganisms. Mar Drugs 2015; 13: 8: 4754-4783.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Xia M-W., Cui C-B., Li C-W., Wu C-J. Three new and eleven known unusual C25 steroids: activated production of silent metabolites in a marine-derived fungus by chemical mutagenesis strategy using diethyl sulphate. Mar Drugs 2014; 12: 3: 1545-1568.</mixed-citation><mixed-citation xml:lang="en">Xia M-W., Cui C-B., Li C-W., Wu C-J. Three new and eleven known unusual C25 steroids: activated production of silent metabolites in a marine-derived fungus by chemical mutagenesis strategy using diethyl sulphate. Mar Drugs 2014; 12: 3: 1545-1568.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Dong Y., Cui C-B, Li C-W et al. Activation of dormant secondary metabolite production by introducing neomycin resistance into the deep-sea fungus, Aspergillus versicolor ZBY-3. Mar Drugs 2014; 12: 8: 4326-4352.</mixed-citation><mixed-citation xml:lang="en">Dong Y., Cui C-B, Li C-W et al. Activation of dormant secondary metabolite production by introducing neomycin resistance into the deep-sea fungus, Aspergillus versicolor ZBY-3. Mar Drugs 2014; 12: 8: 4326-4352.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Bean J., Mahid N., Burda W.N. et al. Epigenetic tailoring for the production of anti-infective cytosporones from the marine fungus Leucostoma persoonii. Mar Drugs 2012; 10: 4: 762-774.</mixed-citation><mixed-citation xml:lang="en">Bean J., Mahid N., Burda W.N. et al. Epigenetic tailoring for the production of anti-infective cytosporones from the marine fungus Leucostoma persoonii. Mar Drugs 2012; 10: 4: 762-774.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang W., Ye P., Chen C.T. et al. Two novel hepatocellular carcinoma cycle inhibitory cyclodepsipeptides from a hydrothermal vent crab-associated fungus Aspergillus clavatus C2WU. Mar Drugs 2013; 11: 12: 4761-4772.</mixed-citation><mixed-citation xml:lang="en">Jiang W., Ye P., Chen C.T. et al. Two novel hepatocellular carcinoma cycle inhibitory cyclodepsipeptides from a hydrothermal vent crab-associated fungus Aspergillus clavatus C2WU. Mar Drugs 2013; 11: 12: 4761-4772.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Ye P., Shen L., Jiang W. et al. Zn-driven discovery of a hydrothermal vent fungal metabolite clavatustide C, and an experimental study of the anticancer mechanism of clavatustide B. Mar Drugs 2014; 12: 6: 3203-3217.</mixed-citation><mixed-citation xml:lang="en">Ye P., Shen L., Jiang W. et al. Zn-driven discovery of a hydrothermal vent fungal metabolite clavatustide C, and an experimental study of the anticancer mechanism of clavatustide B. Mar Drugs 2014; 12: 6: 3203-3217.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Wu B., Wu X., Sun M. et al. Two novel tyrosinase inhibitory sesquiterpenes induced by CuCl2 from a marine-derived fungus Pestalotiopsis sp.Z233. Mar Drugs 2013; 11: 8: 2713-2721.</mixed-citation><mixed-citation xml:lang="en">Wu B., Wu X., Sun M. et al. Two novel tyrosinase inhibitory sesquiterpenes induced by CuCl2 from a marine-derived fungus Pestalotiopsis sp.Z233. Mar Drugs 2013; 11: 8: 2713-2721.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Marmann A., Aly A.N., Lin W. et al. Co-cultivation - a powerful emerging tool for enhancing the chemical diversity of microorganisms. Mar Drugs 2014; 12: 2: 1043-1065.</mixed-citation><mixed-citation xml:lang="en">Marmann A., Aly A.N., Lin W. et al. Co-cultivation - a powerful emerging tool for enhancing the chemical diversity of microorganisms. Mar Drugs 2014; 12: 2: 1043-1065.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ola A.R.B., Thomy D., Lai D. et al. Inducing secondary metabolite production by endophytic fungus Fusarium tricinctum coculture with Bacillus subtilis. J Nat Prod 2013; 76: 11: 2094-2099.</mixed-citation><mixed-citation xml:lang="en">Ola A.R.B., Thomy D., Lai D. et al. Inducing secondary metabolite production by endophytic fungus Fusarium tricinctum coculture with Bacillus subtilis. J Nat Prod 2013; 76: 11: 2094-2099.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Oh D-C., Kaufman C.A., Jensen P.R., Fenical W. Induced production of emericellamides A and B from the marine-derived fungus Emericella sp. In competing co-culture. J Nat Prod 2007; 70: 4: 515-520.</mixed-citation><mixed-citation xml:lang="en">Oh D-C., Kaufman C.A., Jensen P.R., Fenical W. Induced production of emericellamides A and B from the marine-derived fungus Emericella sp. In competing co-culture. J Nat Prod 2007; 70: 4: 515-520.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Wang W-J., Li D-Y., Li Y-C. et al. Caryophyllene sesquiterpenes from the marine-derived fungus Ascotricha sp. ZJ-M-5 by the one strain - many compounds strategy. J Nat Prod 2014; 77: 6: 1367-1371.</mixed-citation><mixed-citation xml:lang="en">Wang W-J., Li D-Y., Li Y-C. et al. Caryophyllene sesquiterpenes from the marine-derived fungus Ascotricha sp. ZJ-M-5 by the one strain - many compounds strategy. J Nat Prod 2014; 77: 6: 1367-1371.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Y., Li X-M., Meng L-H. et al. Bisthiodiketopiperazines and acorane sesquiterpenes produced by from the marine-derived fungus Penicillium adametzioides AS-53 on different culture media. J Nat Prod 2015; 78: 6: 1294-1299.</mixed-citation><mixed-citation xml:lang="en">Liu Y., Li X-M., Meng L-H. et al. Bisthiodiketopiperazines and acorane sesquiterpenes produced by from the marine-derived fungus Penicillium adametzioides AS-53 on different culture media. J Nat Prod 2015; 78: 6: 1294-1299.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Liang W-L., Le X., Li H-J. et al. Exploring the chemodiversity and biological activities of secondary metabolites from the marine fungus Neosartorya pseudofischeri. Mar Drugs 2014; 12: 11: 5657-5676.</mixed-citation><mixed-citation xml:lang="en">Liang W-L., Le X., Li H-J. et al. Exploring the chemodiversity and biological activities of secondary metabolites from the marine fungus Neosartorya pseudofischeri. Mar Drugs 2014; 12: 11: 5657-5676.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Y-N., Shao C-L., Zheng C-J. et al. Diversity and antibacterial activities of fungi derived from the Gorgonian Echinogorgia rebekka from the South China Sea. Mar Drugs 2011; 9: 8: 1379-1390.</mixed-citation><mixed-citation xml:lang="en">Wang Y-N., Shao C-L., Zheng C-J. et al. Diversity and antibacterial activities of fungi derived from the Gorgonian Echinogorgia rebekka from the South China Sea. Mar Drugs 2011; 9: 8: 1379-1390.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">ao J., Sun U-L., Zhang X-Yet. al. Antifouling and antibacterial polyketides from marine gorgonian coral-associated fungus Penicillium sp. SCSGAF 0023. J Antibiot 2013; 66: 4: 219-223.</mixed-citation><mixed-citation xml:lang="en">ao J., Sun U-L., Zhang X-Yet. al. Antifouling and antibacterial polyketides from marine gorgonian coral-associated fungus Penicillium sp. SCSGAF 0023. J Antibiot 2013; 66: 4: 219-223.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Cao F., Yang Q., Shao C-L et al. Bioactive 7-oxabicyclic{6.3.0]lactam and 12-membered macrolides from a gorgonian-derived Cladosporium sp. fungus. Mar Drugs 2015; 13: 7: 4171-4178.</mixed-citation><mixed-citation xml:lang="en">Cao F., Yang Q., Shao C-L et al. Bioactive 7-oxabicyclic{6.3.0]lactam and 12-membered macrolides from a gorgonian-derived Cladosporium sp. fungus. Mar Drugs 2015; 13: 7: 4171-4178.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao D-L., Shao C-L., Zhang Q. et al. Asaphilone and diphenyl ether derivatives from a gorgonian-derived strain of the fungus Penicillium pinophilum. J Nat Prod 2015; 78: 9: 2310-2314.</mixed-citation><mixed-citation xml:lang="en">Zhao D-L., Shao C-L., Zhang Q. et al. Asaphilone and diphenyl ether derivatives from a gorgonian-derived strain of the fungus Penicillium pinophilum. J Nat Prod 2015; 78: 9: 2310-2314.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Chen M., Shao C-L., Meng H. et al. Anti-respiratory syncytial virus prenylated dihygroquinolone derivatives from the gorgonian-derived fungus Aspergillus sp. XS-20090B15. J Nat Prod 2014; 77: 12: 2720-2724.</mixed-citation><mixed-citation xml:lang="en">Chen M., Shao C-L., Meng H. et al. Anti-respiratory syncytial virus prenylated dihygroquinolone derivatives from the gorgonian-derived fungus Aspergillus sp. XS-20090B15. J Nat Prod 2014; 77: 12: 2720-2724.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Chen M., Wang K-L., Liu M. et al. Bioactive steroid derivatives and buty-rolactone derivatives from a gorgonian-derived Aspergillus sp. fungus. Chem Biodivers 2015; 12: 9: 1398-1406.</mixed-citation><mixed-citation xml:lang="en">Chen M., Wang K-L., Liu M. et al. Bioactive steroid derivatives and buty-rolactone derivatives from a gorgonian-derived Aspergillus sp. fungus. Chem Biodivers 2015; 12: 9: 1398-1406.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Nong X-H., Zheng Z-H., Zhang X-Y. et al. Polyketides from a marine-derived fungus Xylariaceaesp. Mar Drugs 2013; 11: 5: 1718-1727.</mixed-citation><mixed-citation xml:lang="en">Nong X-H., Zheng Z-H., Zhang X-Y. et al. Polyketides from a marine-derived fungus Xylariaceaesp. Mar Drugs 2013; 11: 5: 1718-1727.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Chen M., Shao C-L., Fu X-M. et al. Lumazine peptides penilumamides BD and the cyclic pentapeptide asperpeptide A from a gorgonian-derived Aspergillus sp. fungus. J Nat Prod 2014; 77: 7: 1601-1606.</mixed-citation><mixed-citation xml:lang="en">Chen M., Shao C-L., Fu X-M. et al. Lumazine peptides penilumamides BD and the cyclic pentapeptide asperpeptide A from a gorgonian-derived Aspergillus sp. fungus. J Nat Prod 2014; 77: 7: 1601-1606.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Li H-J., Xie Y-L., Xie Z-L. et al. Chondrosterins A-E, triquinane-type sesquiterpenoids from soft coral-associated fungus Chondrostereum sp. Mar Drugs 2012; 10: 3: 627-638.</mixed-citation><mixed-citation xml:lang="en">Li H-J., Xie Y-L., Xie Z-L. et al. Chondrosterins A-E, triquinane-type sesquiterpenoids from soft coral-associated fungus Chondrostereum sp. Mar Drugs 2012; 10: 3: 627-638.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Li H-J., Chen T., Xie Y-L. et al. Isolation and structural elucidation of chondrosterins F-H from the marine fungus Chondrostereum sp. Mar Drugs 2013; 11: 2: 551-558.</mixed-citation><mixed-citation xml:lang="en">Li H-J., Chen T., Xie Y-L. et al. Isolation and structural elucidation of chondrosterins F-H from the marine fungus Chondrostereum sp. Mar Drugs 2013; 11: 2: 551-558.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng C-J., Shao C-L., Chen M. et al. Merosesquiterpenoids and tenmembered macrolides from a soft coral-derived Lophiostoma sp. fungus. Chem Biodivers 2015; 12: 9: 1407-1414.</mixed-citation><mixed-citation xml:lang="en">Zheng C-J., Shao C-L., Chen M. et al. Merosesquiterpenoids and tenmembered macrolides from a soft coral-derived Lophiostoma sp. fungus. Chem Biodivers 2015; 12: 9: 1407-1414.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu M., Gao H., Wu C. et al. Lipid-lowering polyketides from a soft coral-derived fungus Cladosporium sp. TZP29. Bioorg Med Chem Lett 2015; 25: 17: 3606-3609.</mixed-citation><mixed-citation xml:lang="en">Zhu M., Gao H., Wu C. et al. Lipid-lowering polyketides from a soft coral-derived fungus Cladosporium sp. TZP29. Bioorg Med Chem Lett 2015; 25: 17: 3606-3609.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng C-J., Shao C-L., Guo Z-Y. et al. Bioactive hydroanthraquinones and anthraquinone dimers from a soft coral-derived Alternaria sp. fungus. J Nat Prod 2012; 75: 2: 189-197.</mixed-citation><mixed-citation xml:lang="en">Zheng C-J., Shao C-L., Guo Z-Y. et al. Bioactive hydroanthraquinones and anthraquinone dimers from a soft coral-derived Alternaria sp. fungus. J Nat Prod 2012; 75: 2: 189-197.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Liu J., Li F., Kim E.L. et al. Antibacterial polyketides from the jellyfish-derived fungus Paecilomyces variotii. J Nat Prod 2011; 74: 8: 1826-1829.</mixed-citation><mixed-citation xml:lang="en">Liu J., Li F., Kim E.L. et al. Antibacterial polyketides from the jellyfish-derived fungus Paecilomyces variotii. J Nat Prod 2011; 74: 8: 1826-1829.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Wang H., Hong J., Yin J. et al. Dimeric octaketide spiroketals from the jellyfish-derived fungus Paecilomyces variotii J08NF-1. J Nat Prod 2015; 78: 11: 2832-2836.</mixed-citation><mixed-citation xml:lang="en">Wang H., Hong J., Yin J. et al. Dimeric octaketide spiroketals from the jellyfish-derived fungus Paecilomyces variotii J08NF-1. J Nat Prod 2015; 78: 11: 2832-2836.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Teske A., Reysenbach A-L. Editorial: Hydrothermal microbial ecosystems. Front Microbiol 2015; 6: 884.</mixed-citation><mixed-citation xml:lang="en">Teske A., Reysenbach A-L. Editorial: Hydrothermal microbial ecosystems. Front Microbiol 2015; 6: 884.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Thornburg C.C., Zabriskie T.M., McPhail K.L. Deep-sea hydrothermal vents:potential hot spots for natural products discovery. J Nat Prod 2010; 73: 3: 489-499.</mixed-citation><mixed-citation xml:lang="en">Thornburg C.C., Zabriskie T.M., McPhail K.L. Deep-sea hydrothermal vents:potential hot spots for natural products discovery. J Nat Prod 2010; 73: 3: 489-499.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Chen X-W., Li C-W., Cui C-B. et al. Nine new and five known polyketides derived from a deep sea-sourced Aspergillus sp.16-02-1. Mar Drugs 2014; 12: 6: 3116-3137.</mixed-citation><mixed-citation xml:lang="en">Chen X-W., Li C-W., Cui C-B. et al. Nine new and five known polyketides derived from a deep sea-sourced Aspergillus sp.16-02-1. Mar Drugs 2014; 12: 6: 3116-3137.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Liaw C-C., Yang Y-L., Lin C-K. et al. New meroterpenoids from Aspergillus terreus with inhibition of cyclooxygenase-2 expression. Org Lett 2015; 17: 10: 2330-2333.</mixed-citation><mixed-citation xml:lang="en">Liaw C-C., Yang Y-L., Lin C-K. et al. New meroterpenoids from Aspergillus terreus with inhibition of cyclooxygenase-2 expression. Org Lett 2015; 17: 10: 2330-2333.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y., Ye D., Shao Z. et al. A sterol and spiroditerpenoids from a Penicillium sp. isolated from a deep sea sediment sample. Mar Drugs 2012; 10: 2: 497-506.</mixed-citation><mixed-citation xml:lang="en">Li Y., Ye D., Shao Z. et al. A sterol and spiroditerpenoids from a Penicillium sp. isolated from a deep sea sediment sample. Mar Drugs 2012; 10: 2: 497-506.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Wu B., Oesker V., Wiese J. et al. Two new antibiotic pyridones produced by a marine fungus, Trichoderma sp. strain MF106. Mar Drugs 2014; 12: 3: 1208-1219.</mixed-citation><mixed-citation xml:lang="en">Wu B., Oesker V., Wiese J. et al. Two new antibiotic pyridones produced by a marine fungus, Trichoderma sp. strain MF106. Mar Drugs 2014; 12: 3: 1208-1219.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Figueroa L., Jime 'nez C., Rodriques J. et al. 3-Nitroasterric acid derivatives from an antarctic sponge-derived Pseudogymnoascus sp. fungus. J Nat Prod 2015; 78: 4: 919-923.</mixed-citation><mixed-citation xml:lang="en">Figueroa L., Jime 'nez C., Rodriques J. et al. 3-Nitroasterric acid derivatives from an antarctic sponge-derived Pseudogymnoascus sp. fungus. J Nat Prod 2015; 78: 4: 919-923.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Wu G., Lin A., Gu Q. et al. Four new chloro-eremophilane sesquiterpenes from an antarctic deep-sea derived fungus, Penicillium sp. PR19N-1. Mar Drugs 2013; 11: 4: 1399-1408.</mixed-citation><mixed-citation xml:lang="en">Wu G., Lin A., Gu Q. et al. Four new chloro-eremophilane sesquiterpenes from an antarctic deep-sea derived fungus, Penicillium sp. PR19N-1. Mar Drugs 2013; 11: 4: 1399-1408.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Schulz D., Ohlendorf B., Zinecker H. et al. Eutypoids B-E produced by a Penicillium sp. strain from the North sea. J Nat Prod 2011; 74: 1: 99-101.</mixed-citation><mixed-citation xml:lang="en">Schulz D., Ohlendorf B., Zinecker H. et al. Eutypoids B-E produced by a Penicillium sp. strain from the North sea. J Nat Prod 2011; 74: 1: 99-101.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J., Wei X., Qin X. et al. Antiviral merosesquiterpenoids produced by the antarctic fungus Aspergillus ochraceopetaliformis SCSIO 05702. J Nat Prod 2016; 79: 1: 59-65.</mixed-citation><mixed-citation xml:lang="en">Wang J., Wei X., Qin X. et al. Antiviral merosesquiterpenoids produced by the antarctic fungus Aspergillus ochraceopetaliformis SCSIO 05702. J Nat Prod 2016; 79: 1: 59-65.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Lu X-L., Liu J-T., Liu X-Y. et al. Pimarane diterpenes from the arctic fungus Eutypella sp. D-1. J Antibiot 2014; 67: 2: 171-174.</mixed-citation><mixed-citation xml:lang="en">Lu X-L., Liu J-T., Liu X-Y. et al. Pimarane diterpenes from the arctic fungus Eutypella sp. D-1. J Antibiot 2014; 67: 2: 171-174.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Stierle D.B., Stierle A.A., Patacini B. The berkeleyacetals, three meroterpenes from a deep water acid mine waste Penicillium. J Nat Prod 2007; 70: 11: 1820-1823.</mixed-citation><mixed-citation xml:lang="en">Stierle D.B., Stierle A.A., Patacini B. The berkeleyacetals, three meroterpenes from a deep water acid mine waste Penicillium. J Nat Prod 2007; 70: 11: 1820-1823.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Stierle A.A., Stierle D.B., Patacini B. The berkeleyamides, amides from the acid lake fungus Penicillium rubrum. J Nat Prod 2008; 71: 5: 856-860.</mixed-citation><mixed-citation xml:lang="en">Stierle A.A., Stierle D.B., Patacini B. The berkeleyamides, amides from the acid lake fungus Penicillium rubrum. J Nat Prod 2008; 71: 5: 856-860.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Stierle D.B., Stierle A.A., Girtsman T. et al. Caspase-1 and -3 inhibiting drimane sesquiterpenoids from the extremophilic fungus Penicillium solitum. J Nat Prod 2012; 75: 2: 262-266.</mixed-citation><mixed-citation xml:lang="en">Stierle D.B., Stierle A.A., Girtsman T. et al. Caspase-1 and -3 inhibiting drimane sesquiterpenoids from the extremophilic fungus Penicillium solitum. J Nat Prod 2012; 75: 2: 262-266.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Stierle D.B, Stierle A.A., Girtsman T. Caspase-1 inhibitors from an extremophilic fungus that target specific leukemia cell lines. J Nat Prod 2012; 75: 3: 344-350.</mixed-citation><mixed-citation xml:lang="en">Stierle D.B, Stierle A.A., Girtsman T. Caspase-1 inhibitors from an extremophilic fungus that target specific leukemia cell lines. J Nat Prod 2012; 75: 3: 344-350.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Stierle A.A., Stierle D.B., Girtsman T. et al. Azaphilones from an acid mine extremophile strain of a Pleurostomophora sp. J Nat Prod 2015; 78: 12: 2917-2923.</mixed-citation><mixed-citation xml:lang="en">Stierle A.A., Stierle D.B., Girtsman T. et al. Azaphilones from an acid mine extremophile strain of a Pleurostomophora sp. J Nat Prod 2015; 78: 12: 2917-2923.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Tang Q., Guo K., Li X-Y et al. Three new asperentin derivatives from the algicolous fungus Aspergillus sp. F00785. Mar Drugs 2014; 12: 12: 5993-6002.</mixed-citation><mixed-citation xml:lang="en">Tang Q., Guo K., Li X-Y et al. Three new asperentin derivatives from the algicolous fungus Aspergillus sp. F00785. Mar Drugs 2014; 12: 12: 5993-6002.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Wang W., Wang Y., Tao H. et al. Cerebrosides of the halotolerant fungus Alternaria raphani isolated from a sea salt field. J Nat Prod 2009; 72: 9: 1695-1698.</mixed-citation><mixed-citation xml:lang="en">Wang W., Wang Y., Tao H. et al. Cerebrosides of the halotolerant fungus Alternaria raphani isolated from a sea salt field. J Nat Prod 2009; 72: 9: 1695-1698.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Wang W., Zhu T., Tao H. et al. Two new cytotoxic quinine type compounds from the halotolerant fungus Aspergillus variecolor. J Antibiot 2007; 60: 10: 603-607.</mixed-citation><mixed-citation xml:lang="en">Wang W., Zhu T., Tao H. et al. Two new cytotoxic quinine type compounds from the halotolerant fungus Aspergillus variecolor. J Antibiot 2007; 60: 10: 603-607.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Xin Z-H., Wang W-L., Zhang Y-P. et al. Pennicitrinone D, a new citrinin dimmer from the halotolerant fungus Penicillium notatum B-52. J Antibiot 2009; 62: 4: 225-227.</mixed-citation><mixed-citation xml:lang="en">Xin Z-H., Wang W-L., Zhang Y-P. et al. Pennicitrinone D, a new citrinin dimmer from the halotolerant fungus Penicillium notatum B-52. J Antibiot 2009; 62: 4: 225-227.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Y., Lu Z., Sun K., Zhu W. Effect of high salt stress on secondary metabolite production in the marine-derived fungus Spicaria elegans. Mar Drugs 2011; 9: 4: 535-542.</mixed-citation><mixed-citation xml:lang="en">Wang Y., Lu Z., Sun K., Zhu W. Effect of high salt stress on secondary metabolite production in the marine-derived fungus Spicaria elegans. Mar Drugs 2011; 9: 4: 535-542.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y., Ye D., Chen X. et al. Breviane spiroditerpenoids from an extremetolerant Penicillium sp. isolated from a deep sea sediment sample. J Nat Prod 2009; 72: 5: 912-916.</mixed-citation><mixed-citation xml:lang="en">Li Y., Ye D., Chen X. et al. Breviane spiroditerpenoids from an extremetolerant Penicillium sp. isolated from a deep sea sediment sample. J Nat Prod 2009; 72: 5: 912-916.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Y., Zheng J., Liu Pm et al. Three new compounds from Aspergillus terreus PT06-2 grown in a high salt medium. Mar Drugs 2011; 9: 8: 1368-1378.</mixed-citation><mixed-citation xml:lang="en">Wang Y., Zheng J., Liu Pm et al. Three new compounds from Aspergillus terreus PT06-2 grown in a high salt medium. Mar Drugs 2011; 9: 8: 1368-1378.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Yamazaki H., Rotinsulu H., Narita R. et al. Induced production of halogenated epidithiodiketopiperazines by a marine-derived Trichoderma cf. brevicompactum with sodium halides. J Nat Prod 2015; 78: 10: 2319-2321.</mixed-citation><mixed-citation xml:lang="en">Yamazaki H., Rotinsulu H., Narita R. et al. Induced production of halogenated epidithiodiketopiperazines by a marine-derived Trichoderma cf. brevicompactum with sodium halides. J Nat Prod 2015; 78: 10: 2319-2321.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Nenkep V., Yun K., Zhang D. et al. Induced production of bro-momethylchlamydosporols A and B from the marine-derived fungus Fusarium tricinctum. J Nat Prod 2010; 73: 12: 2061-2063.</mixed-citation><mixed-citation xml:lang="en">Nenkep V., Yun K., Zhang D. et al. Induced production of bro-momethylchlamydosporols A and B from the marine-derived fungus Fusarium tricinctum. J Nat Prod 2010; 73: 12: 2061-2063.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Wagner C., El Omari M., König G.M. Biohalogenation: nature's way to synthesize halogenated metabolites. J Nat Prod 2009; 72: 3: 540-553.</mixed-citation><mixed-citation xml:lang="en">Wagner C., El Omari M., König G.M. Biohalogenation: nature's way to synthesize halogenated metabolites. J Nat Prod 2009; 72: 3: 540-553.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Chen Z., Song Y., Chen Y. et al. Cyclic heptapeptides, cordyheptapeptides C-E, from the marine-derived fungus Acremonium persicinum SCSIO 115 and their cytotoxic activities. J Nat Prod 2012; 75: 6: 1215-1219.</mixed-citation><mixed-citation xml:lang="en">Chen Z., Song Y., Chen Y. et al. Cyclic heptapeptides, cordyheptapeptides C-E, from the marine-derived fungus Acremonium persicinum SCSIO 115 and their cytotoxic activities. J Nat Prod 2012; 75: 6: 1215-1219.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Patnayake R., Fremlin L.J., Lacey E. et al. Acremolides A-D, lipodepsipeptides from an australian marine-derived fungus, Acremonium sp. J Nat Prod 2008; 71: 3: 403-408.</mixed-citation><mixed-citation xml:lang="en">Patnayake R., Fremlin L.J., Lacey E. et al. Acremolides A-D, lipodepsipeptides from an australian marine-derived fungus, Acremonium sp. J Nat Prod 2008; 71: 3: 403-408.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Julianti E., Oh H., Jang K.H. et al. Acremostrictin, a highly oxygenated metabolite from the marine fungus Acremonium strictum. J Nat Prod 2011; 74: 12: 2592-2594.</mixed-citation><mixed-citation xml:lang="en">Julianti E., Oh H., Jang K.H. et al. Acremostrictin, a highly oxygenated metabolite from the marine fungus Acremonium strictum. J Nat Prod 2011; 74: 12: 2592-2594.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Kim H., Yang I., Ryu S.-Y. et al. Acredinones A and B, voltage-dependent potassium channel inhibitors from the sponge-derived fungus Acremonium sp. J Nat Prod 2015; 78: 3: 363-367.</mixed-citation><mixed-citation xml:lang="en">Kim H., Yang I., Ryu S.-Y. et al. Acredinones A and B, voltage-dependent potassium channel inhibitors from the sponge-derived fungus Acremonium sp. J Nat Prod 2015; 78: 3: 363-367.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang P., Bao B., Dang H.T. et al. Anti-inflammatory sesquiterpenoids from a sponge-derived fungus Acremonium sp. J Nat Prod 2009; 72: 2: 270-275.</mixed-citation><mixed-citation xml:lang="en">Zhang P., Bao B., Dang H.T. et al. Anti-inflammatory sesquiterpenoids from a sponge-derived fungus Acremonium sp. J Nat Prod 2009; 72: 2: 270-275.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Trisuwan K., Khamthong N., Rukachaisirikul V. et al. Anthraquinone, cyclopentanone and naphthoquinone derivatives from the sea fan-derived fungi Fusarium spp. PSU-F14 and PSU-F135. J Nat Prod 2010; 73: 9: 1507-1511.</mixed-citation><mixed-citation xml:lang="en">Trisuwan K., Khamthong N., Rukachaisirikul V. et al. Anthraquinone, cyclopentanone and naphthoquinone derivatives from the sea fan-derived fungi Fusarium spp. PSU-F14 and PSU-F135. J Nat Prod 2010; 73: 9: 1507-1511.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Wu G., Sun X., Yu G. et al. Cladosins A-E, hybrid polyketides from a deep-sea -derived fungus, Cladosporium sphaerospermum. J Nat Prod 2014; 77: 2: 270-275.</mixed-citation><mixed-citation xml:lang="en">Wu G., Sun X., Yu G. et al. Cladosins A-E, hybrid polyketides from a deep-sea -derived fungus, Cladosporium sphaerospermum. J Nat Prod 2014; 77: 2: 270-275.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Fredimoses M., Zhou X., Lin X. et al. New prenylxanthones from the deep-sea derived fungus Emericella sp. SCSIO 05240. Mar Drugs 2014; 12: 6: 3190-3202.</mixed-citation><mixed-citation xml:lang="en">Fredimoses M., Zhou X., Lin X. et al. New prenylxanthones from the deep-sea derived fungus Emericella sp. SCSIO 05240. Mar Drugs 2014; 12: 6: 3190-3202.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Wu Q., Wu C., Long R. et al. Varioxiranols A-G and 19-O-methyl-22-methoxypre-shamixanthone, PKS and hybrid PKS-derived metabolites from a sponge-associated Emericella variecolor fungus. J Nat Prod 2015; 78: 10: 2461-2470.</mixed-citation><mixed-citation xml:lang="en">Wu Q., Wu C., Long R. et al. Varioxiranols A-G and 19-O-methyl-22-methoxypre-shamixanthone, PKS and hybrid PKS-derived metabolites from a sponge-associated Emericella variecolor fungus. J Nat Prod 2015; 78: 10: 2461-2470.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Yamazaki H., Saito R., Takahashi O. et al. Trichoketides A and B, two new protein tyrosine phosphatase 1B inhibitors from the marine-derived fungus Trichoderma sp. J Antibiot 2015; 68: 10: 628-632.</mixed-citation><mixed-citation xml:lang="en">Yamazaki H., Saito R., Takahashi O. et al. Trichoketides A and B, two new protein tyrosine phosphatase 1B inhibitors from the marine-derived fungus Trichoderma sp. J Antibiot 2015; 68: 10: 628-632.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Song F., Dai H., Tong Y. et al. Trichodermaketones A-D and 7-0-methylkoninginin D from the fungus Trichoderma koningii. J Nat Prod 2010; 73: 5: 806-810.</mixed-citation><mixed-citation xml:lang="en">Song F., Dai H., Tong Y. et al. Trichodermaketones A-D and 7-0-methylkoninginin D from the fungus Trichoderma koningii. J Nat Prod 2010; 73: 5: 806-810.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Yamazaki H., Rotinsulu H., Kaneko T. et al. A new dibenz[b,e]oxepine derivative, 1-hydroxy-10-methoxy- dibenz[b,e]oxepine-6,11-dione, from a marine-derived fungus Beauveria bassiana TPU942. Mar Drugs 2012; 10: 12: 2691-2697.</mixed-citation><mixed-citation xml:lang="en">Yamazaki H., Rotinsulu H., Kaneko T. et al. A new dibenz[b,e]oxepine derivative, 1-hydroxy-10-methoxy- dibenz[b,e]oxepine-6,11-dione, from a marine-derived fungus Beauveria bassiana TPU942. Mar Drugs 2012; 10: 12: 2691-2697.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Du F-Y., Li X-M., Zhang P. et al. Cyclodepsipeptides and other O-containing heterocyclic metabolites from Beauveria felina EN-135, a marine-derived entomopathogenic fungus. Mar Drugs 2014; 12: 5: 2816-2826.</mixed-citation><mixed-citation xml:lang="en">Du F-Y., Li X-M., Zhang P. et al. Cyclodepsipeptides and other O-containing heterocyclic metabolites from Beauveria felina EN-135, a marine-derived entomopathogenic fungus. Mar Drugs 2014; 12: 5: 2816-2826.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Oin C., Lin X., Lu X. et al. Sesquiterpenoids and xanthones derivatives produced by sponge-derived fungus Stachybotrys sp.HH1 ZSDS1F1-2. J Antibiot 2015; 68: 2: 121-125.</mixed-citation><mixed-citation xml:lang="en">Oin C., Lin X., Lu X. et al. Sesquiterpenoids and xanthones derivatives produced by sponge-derived fungus Stachybotrys sp.HH1 ZSDS1F1-2. J Antibiot 2015; 68: 2: 121-125.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Wu B., Oesker V., Wiese J. Spirocyclic drimanes from the marine fungus Stachybotrys sp. strain MF347. Mar Drugs 2014; 12: 4: 1924-1938.</mixed-citation><mixed-citation xml:lang="en">Wu B., Oesker V., Wiese J. Spirocyclic drimanes from the marine fungus Stachybotrys sp. strain MF347. Mar Drugs 2014; 12: 4: 1924-1938.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Mattern D.J., Valiante V., Unkles S.E., Brakhage A.A. Synthetic biology of fungal natural products. Front Microbiol 2015; 6: 775.</mixed-citation><mixed-citation xml:lang="en">Mattern D.J., Valiante V., Unkles S.E., Brakhage A.A. Synthetic biology of fungal natural products. Front Microbiol 2015; 6: 775.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
