Biotransformation of (–)-Isopulegol by Rhodococcus rhodochrous
The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (–)-isopulegol has been established for the first time. R. rhodochrous strain IEGM 1362 was selected as a bacterium capable of metabolizing (–)-isopulegol to form new, previously unknown, 10-hydroxy (2) and 10-c...
Saved in:
Published in | Pharmaceuticals (Basel, Switzerland) Vol. 15; no. 8; p. 964 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Basel
MDPI AG
03.08.2022
MDPI |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (–)-isopulegol has been established for the first time. R. rhodochrous strain IEGM 1362 was selected as a bacterium capable of metabolizing (–)-isopulegol to form new, previously unknown, 10-hydroxy (2) and 10-carboxy (3) derivatives, which may presumably have antitumor activity and act as respiratory stimulants and cancer prevention agents. In the experiments, optimal conditions were selected to provide the maximum target catalytic activity of rhodococci. Using up-to-date (TEM, AFM-CLSM, and EDX) and traditional (cell size, roughness, and zeta potential measurements) biophysical and microbiological methods, it was shown that (–)-isopulegol and halloysite nanotubes did not negatively affect the bacterial cells. The data obtained expand our knowledge of the biocatalytic potential of rhodococci and their possible involvement in the synthesis of pharmacologically active compounds from plant derivatives. |
---|---|
AbstractList | The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (–)-isopulegol has been established for the first time. R. rhodochrous strain IEGM 1362 was selected as a bacterium capable of metabolizing (–)-isopulegol to form new, previously unknown, 10-hydroxy (2) and 10-carboxy (3) derivatives, which may presumably have antitumor activity and act as respiratory stimulants and cancer prevention agents. In the experiments, optimal conditions were selected to provide the maximum target catalytic activity of rhodococci. Using up-to-date (TEM, AFM-CLSM, and EDX) and traditional (cell size, roughness, and zeta potential measurements) biophysical and microbiological methods, it was shown that (–)-isopulegol and halloysite nanotubes did not negatively affect the bacterial cells. The data obtained expand our knowledge of the biocatalytic potential of rhodococci and their possible involvement in the synthesis of pharmacologically active compounds from plant derivatives. The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (–)-isopulegol has been established for the first time. R . rhodochrous strain IEGM 1362 was selected as a bacterium capable of metabolizing (–)-isopulegol to form new, previously unknown, 10-hydroxy ( 2 ) and 10-carboxy ( 3 ) derivatives, which may presumably have antitumor activity and act as respiratory stimulants and cancer prevention agents. In the experiments, optimal conditions were selected to provide the maximum target catalytic activity of rhodococci. Using up-to-date (TEM, AFM-CLSM, and EDX) and traditional (cell size, roughness, and zeta potential measurements) biophysical and microbiological methods, it was shown that (–)-isopulegol and halloysite nanotubes did not negatively affect the bacterial cells. The data obtained expand our knowledge of the biocatalytic potential of rhodococci and their possible involvement in the synthesis of pharmacologically active compounds from plant derivatives. The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (-)-isopulegol has been established for the first time. R. rhodochrous strain IEGM 1362 was selected as a bacterium capable of metabolizing (-)-isopulegol to form new, previously unknown, 10-hydroxy (2) and 10-carboxy (3) derivatives, which may presumably have antitumor activity and act as respiratory stimulants and cancer prevention agents. In the experiments, optimal conditions were selected to provide the maximum target catalytic activity of rhodococci. Using up-to-date (TEM, AFM-CLSM, and EDX) and traditional (cell size, roughness, and zeta potential measurements) biophysical and microbiological methods, it was shown that (-)-isopulegol and halloysite nanotubes did not negatively affect the bacterial cells. The data obtained expand our knowledge of the biocatalytic potential of rhodococci and their possible involvement in the synthesis of pharmacologically active compounds from plant derivatives.The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (-)-isopulegol has been established for the first time. R. rhodochrous strain IEGM 1362 was selected as a bacterium capable of metabolizing (-)-isopulegol to form new, previously unknown, 10-hydroxy (2) and 10-carboxy (3) derivatives, which may presumably have antitumor activity and act as respiratory stimulants and cancer prevention agents. In the experiments, optimal conditions were selected to provide the maximum target catalytic activity of rhodococci. Using up-to-date (TEM, AFM-CLSM, and EDX) and traditional (cell size, roughness, and zeta potential measurements) biophysical and microbiological methods, it was shown that (-)-isopulegol and halloysite nanotubes did not negatively affect the bacterial cells. The data obtained expand our knowledge of the biocatalytic potential of rhodococci and their possible involvement in the synthesis of pharmacologically active compounds from plant derivatives. |
Author | Korchagina, Dina V. Luchnikova, Natalia A. Ivshina, Irina B. Gatilov, Yurii V. Sorokin, Vladimir V. Ilyina, Irina V. Volcho, Konstantin P. Maltseva, Polina Yu Kostrikina, Nadezhda A. Salakhutdinov, Nariman F. Mulyukin, Andrey L. |
AuthorAffiliation | 3 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of the Siberian Branch of the Russian Academy of Sciences, 9 Lavrentiev Avenue, 630090 Novosibirsk, Russia; ilyina@nioch.nsc.ru (I.V.I.); volcho@nioch.nsc.ru (K.P.V.); gatilov@nioch.nsc.ru (Y.V.G.); verbenon@mail.ru (D.V.K.); anvar@nioch.nsc.ru (N.F.S.) 1 Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Perm Federal Research Center of the Ural Branch of the Russian Academy of Sciences, 13 Golev Str., 614081 Perm, Russia; luchnikova.n@mail.ru 2 Department of Microbiology and Immunology, Perm State National Research University, 15 Bukirev Str., 614990 Perm, Russia; inbox.98@bk.ru 4 Winogradsky Institute of Microbiology, Research Center of Biotechnology, Russian Academy of Sciences, 60 let Oktyabrya, 7, bld. 2, 117312 Moscow, Russia; nadin-kost@yandex.ru (N.A.K.); vlvlsorokin@gmail.com (V.V.S.); andlm@mail.ru (A.L.M.) |
AuthorAffiliation_xml | – name: 3 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of the Siberian Branch of the Russian Academy of Sciences, 9 Lavrentiev Avenue, 630090 Novosibirsk, Russia; ilyina@nioch.nsc.ru (I.V.I.); volcho@nioch.nsc.ru (K.P.V.); gatilov@nioch.nsc.ru (Y.V.G.); verbenon@mail.ru (D.V.K.); anvar@nioch.nsc.ru (N.F.S.) – name: 4 Winogradsky Institute of Microbiology, Research Center of Biotechnology, Russian Academy of Sciences, 60 let Oktyabrya, 7, bld. 2, 117312 Moscow, Russia; nadin-kost@yandex.ru (N.A.K.); vlvlsorokin@gmail.com (V.V.S.); andlm@mail.ru (A.L.M.) – name: 1 Institute of Ecology and Genetics of Microorganisms of the Ural Branch of the Russian Academy of Sciences, Perm Federal Research Center of the Ural Branch of the Russian Academy of Sciences, 13 Golev Str., 614081 Perm, Russia; luchnikova.n@mail.ru – name: 2 Department of Microbiology and Immunology, Perm State National Research University, 15 Bukirev Str., 614990 Perm, Russia; inbox.98@bk.ru |
Author_xml | – sequence: 1 givenname: Irina B. orcidid: 0000-0003-2558-4789 surname: Ivshina fullname: Ivshina, Irina B. – sequence: 2 givenname: Natalia A. orcidid: 0000-0002-9292-5726 surname: Luchnikova fullname: Luchnikova, Natalia A. – sequence: 3 givenname: Polina Yu surname: Maltseva fullname: Maltseva, Polina Yu – sequence: 4 givenname: Irina V. surname: Ilyina fullname: Ilyina, Irina V. – sequence: 5 givenname: Konstantin P. orcidid: 0000-0002-4083-9324 surname: Volcho fullname: Volcho, Konstantin P. – sequence: 6 givenname: Yurii V. surname: Gatilov fullname: Gatilov, Yurii V. – sequence: 7 givenname: Dina V. surname: Korchagina fullname: Korchagina, Dina V. – sequence: 8 givenname: Nadezhda A. surname: Kostrikina fullname: Kostrikina, Nadezhda A. – sequence: 9 givenname: Vladimir V. surname: Sorokin fullname: Sorokin, Vladimir V. – sequence: 10 givenname: Andrey L. orcidid: 0000-0002-3524-1328 surname: Mulyukin fullname: Mulyukin, Andrey L. – sequence: 11 givenname: Nariman F. surname: Salakhutdinov fullname: Salakhutdinov, Nariman F. |
BookMark | eNptkd9qFDEUh4NU7B-98QkGvKnC6DlJJpncSLVUXSgIotchk2R2s8xO1mRG6J3v4Bv6JE13K7alVzkk3_lO-J1jcjDG0RPyEuEtYwrebVfYQAtK8CfkCDnldUu5PLhTH5LjnNcAjUSOz8ghE4ANIj0iZx9DnJIZcx_TxkwhjlXsq9O_v_-8rhc5bufBL-NQdVfVt1V00UZr51ylXb1Kcc7PydPeDNm_uD1PyI9PF9_Pv9SXXz8vzj9c1pZzNdWeARrWcQ6-VWBd02InTEuZtBJ9p4SArnWm7ZBK7xQ41rTQW-MoeuUZZSdksfe6aNZ6m8LGpCsdTdC7i5iW2qQp2MHrTsgelEfqymxLUVl0UoEw1gCnpiuu93vXdu423lk_lgiGe9L7L2NY6WX8pRVHyoEVwemtIMWfs8-T3oRs_TCY0ZdMNJUgBYBEVdBXD9B1nNNYorqhBJWUUVEo2FM2xZyT77UN024dZX4YNIK-WbX-v-rS8uZBy7__PwJfA7fDqiQ |
CitedBy_id | crossref_primary_10_3390_genes15080992 crossref_primary_10_7242_2658_705X_2024_3_2 crossref_primary_10_3390_molecules29143378 crossref_primary_10_3390_ph16091294 crossref_primary_10_3390_ph16060872 crossref_primary_10_3390_microorganisms12122605 |
Cites_doi | 10.1016/j.bmcl.2018.04.057 10.1007/s10593-020-02753-x 10.1016/0031-9422(91)83449-U 10.3109/14756366.2012.727411 10.1016/j.jare.2014.11.009 10.1080/10242420600667684 10.3390/ijms19113522 10.1016/j.watres.2020.116380 10.17485/ijst/2017/v10i21/111382 10.1007/978-3-642-05199-9 10.1002/jsfa.2740101206 10.1139/m87-082 10.3390/polym10020202 10.1007/s13205-021-03108-9 10.3390/nano12060951 10.1016/S1872-2067(19)63305-X 10.4155/fmc-2020-0204 10.1586/ecp.11.6 10.1590/0001-3765201920190105 10.1039/D0RA07739A 10.3390/ijms20194787 10.1016/j.carbpol.2018.06.026 10.1016/j.procbio.2011.06.010 10.3389/fmicb.2019.00077 10.1016/j.fct.2008.06.053 10.1016/j.jhazmat.2017.12.025 10.3144/expresspolymlett.2019.40 10.1016/j.chemosphere.2020.129095 10.1016/j.procbio.2016.10.003 10.1021/acsabm.0c01332 10.1002/tcr.202100194 10.1016/j.scp.2015.07.001 10.1271/bbb.67.475 10.1023/A:1017942114930 10.1016/j.enzmictec.2019.109467 10.3390/molecules23061265 10.1177/0021998318763246 |
ContentType | Journal Article |
Copyright | 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2022 by the authors. 2022 |
Copyright_xml | – notice: 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2022 by the authors. 2022 |
DBID | AAYXX CITATION 3V. 7XB 8FK 8G5 ABUWG AFKRA AZQEC BENPR CCPQU DWQXO GNUQQ GUQSH M2O MBDVC PHGZM PHGZT PIMPY PKEHL PQEST PQQKQ PQUKI PRINS Q9U 7X8 5PM DOA |
DOI | 10.3390/ph15080964 |
DatabaseName | CrossRef ProQuest Central (Corporate) ProQuest Central (purchase pre-March 2016) ProQuest Central (Alumni) (purchase pre-March 2016) Research Library (Alumni) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central ProQuest One Community College ProQuest Central ProQuest Central Student ProQuest Research Library Research Library Research Library (Corporate) ProQuest Central Premium ProQuest One Academic (New) Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest Central Basic MEDLINE - Academic PubMed Central (Full Participant titles) Acceso a contenido Full Text - Doaj |
DatabaseTitle | CrossRef Publicly Available Content Database Research Library Prep ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Basic ProQuest Central Essentials ProQuest One Academic Eastern Edition ProQuest Central (Alumni Edition) ProQuest One Community College Research Library (Alumni Edition) ProQuest Central China ProQuest Central ProQuest One Academic UKI Edition ProQuest Central Korea ProQuest Research Library ProQuest Central (New) ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | Publicly Available Content Database MEDLINE - Academic CrossRef |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Pharmacy, Therapeutics, & Pharmacology |
EISSN | 1424-8247 |
ExternalDocumentID | oai_doaj_org_article_b67f09e12dc44c219c1d7906aca042ab PMC9412403 10_3390_ph15080964 |
GrantInformation_xml | – fundername: Ministry of Science and Higher Education of the Russian Federation grantid: 075-15-2021-1051 |
GroupedDBID | --- 2WC 53G 5VS 8G5 AADQD AAFWJ AAYXX ABDBF ABUWG ACGFO ACIHN ACUHS ADBBV AEAQA AFKRA AFPKN AFZYC ALMA_UNASSIGNED_HOLDINGS AOIJS AZQEC BAWUL BCNDV BENPR BPHCQ CCPQU CITATION DIK DWQXO EBD ESX GNUQQ GROUPED_DOAJ GUQSH GX1 HH5 HYE IAO IHR ITC KQ8 M2O M48 MK0 MODMG M~E OK1 P2P PGMZT PHGZM PHGZT PIMPY PQQKQ PROAC RPM TUS 3V. 7XB 8FK MBDVC PKEHL PQEST PQUKI PRINS Q9U 7X8 5PM PUEGO |
ID | FETCH-LOGICAL-c449t-e301a3b440e890cd581b6a8237c71eb9660b8da8b127ed90d3580fcad21e9e323 |
IEDL.DBID | M48 |
ISSN | 1424-8247 |
IngestDate | Wed Aug 27 01:20:26 EDT 2025 Thu Aug 21 18:13:57 EDT 2025 Fri Jul 11 00:00:37 EDT 2025 Mon Jun 30 14:54:07 EDT 2025 Tue Jul 01 04:13:28 EDT 2025 Thu Apr 24 23:09:08 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 8 |
Language | English |
License | https://creativecommons.org/licenses/by/4.0 Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c449t-e301a3b440e890cd581b6a8237c71eb9660b8da8b127ed90d3580fcad21e9e323 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0003-2558-4789 0000-0002-9292-5726 0000-0002-3524-1328 0000-0002-4083-9324 |
OpenAccessLink | https://www.proquest.com/docview/2706272326?pq-origsite=%requestingapplication% |
PMID | 36015112 |
PQID | 2706272326 |
PQPubID | 2032350 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_b67f09e12dc44c219c1d7906aca042ab pubmedcentral_primary_oai_pubmedcentral_nih_gov_9412403 proquest_miscellaneous_2707600719 proquest_journals_2706272326 crossref_citationtrail_10_3390_ph15080964 crossref_primary_10_3390_ph15080964 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 20220803 |
PublicationDateYYYYMMDD | 2022-08-03 |
PublicationDate_xml | – month: 8 year: 2022 text: 20220803 day: 3 |
PublicationDecade | 2020 |
PublicationPlace | Basel |
PublicationPlace_xml | – name: Basel |
PublicationTitle | Pharmaceuticals (Basel, Switzerland) |
PublicationYear | 2022 |
Publisher | MDPI AG MDPI |
Publisher_xml | – name: MDPI AG – name: MDPI |
References | Schewe (ref_32) 2011; 46 Bhatia (ref_5) 2008; 46 Hegazy (ref_14) 2015; 6 ref_12 ref_33 Sultana (ref_2) 2013; 28 Movsowitz (ref_29) 2021; 4 ref_31 Ahn (ref_25) 2020; 186 Sassa (ref_35) 2003; 67 Fernandes (ref_34) 2006; 24 Zaprutko (ref_3) 2020; 12 Shahcheraghi (ref_22) 2022; 12 Le (ref_8) 2020; 10 ref_18 ref_16 ref_38 Ilyina (ref_6) 2018; 28 Calixto (ref_1) 2019; 91 Pavlova (ref_7) 2020; 56 Partovinia (ref_26) 2019; 13 Su (ref_15) 2020; 133 Cheremnykh (ref_20) 2018; 346 Liu (ref_28) 2021; 265 Kholkina (ref_10) 2019; 40 Daughton (ref_11) 2011; 4 Hasan (ref_24) 2018; 52 Sawamura (ref_37) 1976; 40 Rawtani (ref_23) 2012; 30 Tian (ref_27) 2018; 198 Mulyukin (ref_30) 2002; 71 Asakawa (ref_36) 1991; 30 ref_41 Tarasova (ref_19) 2017; 52 Szakonyi (ref_4) 2022; 22 Mrunalini (ref_40) 2017; 10 ref_9 Anteneh (ref_17) 2019; 10 Leder (ref_13) 2015; 2 Shukla (ref_21) 1987; 33 Postgate (ref_39) 1959; 10 |
References_xml | – volume: 28 start-page: 2061 year: 2018 ident: ref_6 article-title: Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses publication-title: Bioorg. Med. Chem. Lett. doi: 10.1016/j.bmcl.2018.04.057 – volume: 56 start-page: 936 year: 2020 ident: ref_7 article-title: Synthesis of 1,3-oxazine derivatives based on (−)-isopulegol using the Ritter reaction and study of their analgesic activity publication-title: Chem. Heterocycl. Compd. doi: 10.1007/s10593-020-02753-x – volume: 30 start-page: 3981 year: 1991 ident: ref_36 article-title: Biotransformation of monoterpenoids, (−)- and (+)-Menthols, terpinolene and carvotanacetone by Aspergillus species publication-title: Phytochemistry doi: 10.1016/0031-9422(91)83449-U – volume: 28 start-page: 1113 year: 2013 ident: ref_2 article-title: Enzymatic biotransformation of terpenes as bioactive agents publication-title: J. Enzyme Inhib. Med. Chem. doi: 10.3109/14756366.2012.727411 – volume: 6 start-page: 17 year: 2015 ident: ref_14 article-title: Microbial biotransformation as a tool for drug development based on natural products from mevalonic acid pathway: A review publication-title: J. Adv. Res. doi: 10.1016/j.jare.2014.11.009 – volume: 24 start-page: 237 year: 2006 ident: ref_34 article-title: Microlitre/millilitre shaken bioreactors in fermentative and biotransformation processes—A review publication-title: Biocatal. Biotransformat. doi: 10.1080/10242420600667684 – ident: ref_9 doi: 10.3390/ijms19113522 – volume: 186 start-page: 116380 year: 2020 ident: ref_25 article-title: Fungal mycelia functionalization with halloysite nanotubes for hyphal spreading and sorption behavior regulation: A new bio-ceramic hybrid for enhanced water treatment publication-title: Water Res. doi: 10.1016/j.watres.2020.116380 – volume: 10 start-page: 1 year: 2017 ident: ref_40 article-title: Screening and characterization of lipid inclusions in bacteria by fluorescence microscopy and mass spectrometry as a source for biofuel production publication-title: Indian J. Sci. Technol. doi: 10.17485/ijst/2017/v10i21/111382 – ident: ref_12 doi: 10.1007/978-3-642-05199-9 – volume: 10 start-page: 669 year: 1959 ident: ref_39 article-title: Differential media for sulphur bacteria publication-title: J. Sci. Food Agric. doi: 10.1002/jsfa.2740101206 – volume: 33 start-page: 489 year: 1987 ident: ref_21 article-title: Microbial transformation of menthol and menthane-3,4-diol publication-title: Can. J. Microbiol. doi: 10.1139/m87-082 – ident: ref_33 doi: 10.3390/polym10020202 – volume: 12 start-page: 65 year: 2022 ident: ref_22 article-title: Nano-biotechnology, an applicable approach for sustainable future publication-title: 3 Biotech. doi: 10.1007/s13205-021-03108-9 – ident: ref_31 doi: 10.3390/nano12060951 – volume: 40 start-page: 1713 year: 2019 ident: ref_10 article-title: Prins cyclisation of (−)-isopulegol with benzaldehyde over ZSM-5 based micro-mesoporous catalysts for production of pharmaceuticals publication-title: Chin. J. Catal. doi: 10.1016/S1872-2067(19)63305-X – volume: 30 start-page: 282 year: 2012 ident: ref_23 article-title: Multifarious applications of halloysite nanotubes: A review publication-title: Rev. Adv. Mater. Sci. – volume: 12 start-page: 1743 year: 2020 ident: ref_3 article-title: Anti-COVID drugs: Repurposing existing drugs or search for new complex entities, strategies and perspectives publication-title: Future Med. Chem. doi: 10.4155/fmc-2020-0204 – volume: 4 start-page: 211 year: 2011 ident: ref_11 article-title: Green pharmacy and pharmEcovigilance: Prescribing and the planet publication-title: Expert Rev. Clin. Pharmacol. doi: 10.1586/ecp.11.6 – volume: 91 start-page: e20190105 year: 2019 ident: ref_1 article-title: The role of natural products in modern drug discovery publication-title: An. Acad. Bras. Cienc. doi: 10.1590/0001-3765201920190105 – volume: 10 start-page: 38468 year: 2020 ident: ref_8 article-title: Stereoselective synthesis and application of isopulegol-based bi- and trifunctional chiral compounds publication-title: RSC Adv. doi: 10.1039/D0RA07739A – ident: ref_18 doi: 10.3390/ijms20194787 – volume: 198 start-page: 191 year: 2018 ident: ref_27 article-title: Enhancing bacterial cellulose production via adding mesoporous halloysite nanotubes in the culture medium publication-title: Carbohydr. Polym. doi: 10.1016/j.carbpol.2018.06.026 – volume: 46 start-page: 1885 year: 2011 ident: ref_32 article-title: Biooxidation of monoterpenes with bacterial monooxygenases publication-title: Process. Biochem. doi: 10.1016/j.procbio.2011.06.010 – volume: 10 start-page: 77 year: 2019 ident: ref_17 article-title: Whole cell actinobacteria as biocatalysts publication-title: Front. Microbiol. doi: 10.3389/fmicb.2019.00077 – volume: 46 start-page: S185 year: 2008 ident: ref_5 article-title: Fragrance material review on isopulegol publication-title: Food Chem. Toxicol. doi: 10.1016/j.fct.2008.06.053 – ident: ref_41 – volume: 346 start-page: 103 year: 2018 ident: ref_20 article-title: Bioconversion of ecotoxic dehydroabietic acid using Rhodococcus actinobacteria publication-title: J. Hazard. Mater. doi: 10.1016/j.jhazmat.2017.12.025 – volume: 13 start-page: 484 year: 2019 ident: ref_26 article-title: Fabrication of novel nanocomposite nanofibrous matrices retaining high concentration of microbial cells for heavy crude oil biodegradation publication-title: Express Polym. Lett. doi: 10.3144/expresspolymlett.2019.40 – volume: 265 start-page: 129095 year: 2021 ident: ref_28 article-title: Differential regulation and the underlying mechanisms of clay minerals to Escherichia coli under the stress of polymyxin B: Comparing halloysite with kaolinite publication-title: Chemosphere doi: 10.1016/j.chemosphere.2020.129095 – ident: ref_38 – volume: 52 start-page: 1 year: 2017 ident: ref_19 article-title: Cell adaptations of Rhodococcus rhodochrous IEGM 66 to betulin biotransformation publication-title: Process. Biochem. doi: 10.1016/j.procbio.2016.10.003 – volume: 4 start-page: 4094 year: 2021 ident: ref_29 article-title: Antibody-functionalized halloysite nanotubes for targeting bacterial cells publication-title: ACS Appl. Bio Mater. doi: 10.1021/acsabm.0c01332 – volume: 22 start-page: e202100194 year: 2022 ident: ref_4 article-title: Enantiomeric isopulegol as the chiral pool in the total synthesis of bioactive agents publication-title: Chem. Rec. doi: 10.1002/tcr.202100194 – volume: 2 start-page: 31 year: 2015 ident: ref_13 article-title: Putting benign by design into practice-novel concepts for green and sustainable pharmacy: Designing green drug derivatives by non-targeted synthesis and screening for biodegradability publication-title: Sustain. Chem. Pharm. doi: 10.1016/j.scp.2015.07.001 – volume: 67 start-page: 475 year: 2003 ident: ref_35 article-title: (+)-Menthol and its hydroxy derivatives, novel fungal monoterpenols from the fusicoccin-producing fungi, Phomopsis amygdali F6a and Niigata 2 publication-title: Biosci. Biotechnol. Biochem. doi: 10.1271/bbb.67.475 – volume: 71 start-page: 31 year: 2002 ident: ref_30 article-title: Comparative study of the elemental composition of vegetative and dormant microbial cells publication-title: Microbiology doi: 10.1023/A:1017942114930 – volume: 40 start-page: 649 year: 1976 ident: ref_37 article-title: Conversion of (−)-menthone by Pseudomonas fluorescens M-2 publication-title: Agric. Biol. Chem. – volume: 133 start-page: 109467 year: 2020 ident: ref_15 article-title: Cutinases as stereoselective catalysts: Specific activity and enantioselectivity of cutinases and lipases for menthol and its analogs publication-title: Enzyme Microb. Technol. doi: 10.1016/j.enzmictec.2019.109467 – ident: ref_16 doi: 10.3390/molecules23061265 – volume: 52 start-page: 3199 year: 2018 ident: ref_24 article-title: A study of poly (3-hydroxybutyrate-co-3-hydroxyvalerate) biofilms’ thermal and biodegradable properties reinforced with halloysite nanotubes publication-title: J. Compos. Mater. doi: 10.1177/0021998318763246 |
SSID | ssj0057141 |
Score | 2.320534 |
Snippet | The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (–)-isopulegol has been established for the first time. R. rhodochrous... The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (-)-isopulegol has been established for the first time. R. rhodochrous... The ability of actinobacteria of the genus Rhodococcus to biotransform the monoterpenoid (–)-isopulegol has been established for the first time. R .... |
SourceID | doaj pubmedcentral proquest crossref |
SourceType | Open Website Open Access Repository Aggregation Database Enrichment Source Index Database |
StartPage | 964 |
SubjectTerms | (–)-isopulegol Biodegradation biotransformation Carbon Composite materials Cytotoxicity Enzymes halloysite nanotubes Microorganisms Microscopy monoterpenoid Morphology Nanoparticles Physiology Rhodococcus rhodochrous |
SummonAdditionalLinks | – databaseName: Acceso a contenido Full Text - Doaj dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Ni9swEBVlT72Ubrel7mYXlZbQhZhYtiJZt-2WLmmhJZQEcjP6chMIdoizh9z6H_Yf9pd0xnY-DIVeejP2HOSnmdEbJL0h5L11IytMzsPU6zzkxprQuDQKnYXUaGJt81q--Nt3MZ7xr_PR_KTVF54Ja-SBG-CGRsg8Up7FznJuIb4sc1JFQlsN_qYNZl9Y8_bFVJODR5Jx1oiRJlDUD9cLlD0Hts47y0-t0t-hlt2DkScrzf1z8qyliPRjM7Rz8sQXL0h_0mhM7wZ0erwyVQ1on06O6tO7C3J7tyy3J2y0LGiZ0w-_fz3ehF8qbNflf5Yranb0xwJKUsiH9qGim_oZe_ZUL8ns_vP00zhs2ySEgIjahh5iVCeG88inKgLwgYkKjSI0VjJvUH7TpE6nhsXSOxU53PnMrXYx88oncfKKnBVl4V8T6jU3wP-wymDcCquF0yIxXmqnnEhZQG726GW21RDHVharDGoJRDo7Ih2QdwfbdaOc8VerO5yEgwWqXdcvwAey1geyf_lAQHr7KczaEKyyWKICMxBGEZC3h88QPLgjogsPgKINbkxKpgIiO1PfGVD3S7Fc1DLcCht3R8mb__EHl-RpjPcq8CxK0iNn282DvwK2szXXtWP_Abv5Ams priority: 102 providerName: Directory of Open Access Journals – databaseName: ProQuest Central dbid: BENPR link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3NatwwEBZtcumltGlLnSZFpSU0EBHL1krWKc2WhLTQsIQEcjP6czYQ7O16c9hb3yFv2CfJjFe7G0PpzdgDtmc0n2Y00jeEfHF-4KStBCuCqZiwzjLri5R5B9BoM-Oqjr7417k8uxI_rwfXccGtjdsql5jYAbVvHK6RH2YKCXVh_pdHk98Mu0ZhdTW20HhONgGCC0i-Nocn56OLJRYPFBd8QUqaQ3J_OBkj_TlE7aI3DXVs_b0Qs79B8smMc_qKvIyhIj1e2PY1eRbqLbI3WnBNzw_o5froVHtA9-hozUI9f0O-DW-b2ZOotKlpU9Gvf_887LMfLbbtCjfNHbVzejGG1BRw0d23dNpdY--e9i25Oj25_H7GYrsE5oTQMxbAV01uhUhDoVMwAkSk0iAZjVM8WKThtIU3heWZCl6nHiuglTM-40GHPMvfkY26qcN7QoMRFuJAzDa4cNIZ6Y3MbVDGay8LnpD9pfZKF7nEsaXFXQk5BWq6XGs6IZ9XspMFg8Y_pYZohJUEsl53N5rpTRmdqLRSVakOPPPwxw6w1nGvdCqNM4A9xiZkZ2nCMrpiW64HTkI-rR6DE2FlxNQBFIoyWKBUXCdE9Uzf-6D-k_p23NFxa2zgnebb_3_5B_Iiw5MTuNsk3yEbs-l92IV4ZmY_xkH7CJPL-uM priority: 102 providerName: ProQuest |
Title | Biotransformation of (–)-Isopulegol by Rhodococcus rhodochrous |
URI | https://www.proquest.com/docview/2706272326 https://www.proquest.com/docview/2707600719 https://pubmed.ncbi.nlm.nih.gov/PMC9412403 https://doaj.org/article/b67f09e12dc44c219c1d7906aca042ab |
Volume | 15 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3da9RAEB9q--KL-InReqwoxUJX87G3mzyIetJShZaj9KBvYb_SKxxJvVzBe_N_8D_0L3Emyd010gffQnYCyczO7G8yu78BeGvd0EpTCJ56XXBhrOHGpSF3FkOjibUtGvrik1N5PBHfL4YXW7Dq39kpsL4ztaN-UpP57P3PH8tP6PAfKePElP3D9ZRIzRGLi3uwgyuSIgc9EetqwlC1HSzpUBdPY6FamtJ_nu0tTA1_fw909rdM3lqDjh7Cgw48si-ttR_Bli8fw964ZZ9eHrDzzWGq-oDtsfGGl3r5BD6PrqrFLZxalawq2Ls_v37v8281NfLyl9WMmSU7m2KyipHS3tRs3lxTN5_6KUyODs-_HvOugQK3QmQL7tF7dWKECH2ahWgWxKhSEz2NVZE3RMxpUqdTE8XKuyx0VBMtrHZx5DOfxMkz2C6r0j8H5rUwiAwp_4iElVZLp2VivNIuczKNAthfaS-3Hbs4NbmY5ZhlkKbzjaYDeLOWvW45Ne6UGpER1hLEg93cqOaXeedWuZGqCDMfxQ6_2GL0tZFTWSi11RiNtAlgd2XCfDW38lgRNzNCSRnA6_UwuhXVSnTpUaEkQyVLFWUBqJ7pey_UHymvpg1Bd0YtvcPkxX9950u4H9ORCtqGkuzC9mJ-418h0FmYAeyMDk_HZ4PmR8GgmdN_AQYXAbM |
linkProvider | Scholars Portal |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB5V6QEuiKcIFFgEVFSqVa-9WXsPCAi0SmgbRVUq9ebuy02lyg5xKpQb_4H_wY_il7DjR1JLiFtvlj2S1_P4dsa7-w3AW216mquUebGVqceUVp4yse8Z7aBRBVKnJX3x8YgPTtm3s97ZBvxuzsLgtsoGE0ugNrnGf-R7QYSEum7-5x9n3z3sGoWrq00LjcotDu3yhyvZig_Dr86-74LgYH_yZeDVXQU8zZhYeNa5tAwVY76Nhe_G6hI3LpGzRUfUKmSrVLGRsaJBZI3wDS4UplqagFphQyQ6cJC_yUJXynRgs78_Gp802N-LKKMVCWoYCn9vNkW6dVclsNa0V3YHaKW07Q2ZN2a4g_twr05NyefKlx7Ahs0ewva44rZe7pLJ-qhWsUu2yXjNer18BJ_6l_niRhacZyRPyfs_P3_teMMC24TZi_yKqCU5mbpS2OGwvi7IvLzGXkHFYzi9FUU-gU6WZ_YpECuZcnknVjeUaa4lN5KHykbSCMNj2oWdRnuJrrnLsYXGVeJqGNR0stZ0F96sZGcVY8c_pfpohJUEsmyXN_L5RVIHbaJ4lPrC0sC4L9YO2zU1kfC51NJhnVRd2GpMmNShXyRrR-3C69VjF7S4EiMz6xSKMrggGlHRhahl-taA2k-yy2lJ_y2wYbgfPvv_y1_BncHk-Cg5Go4On8PdAE9t4E6XcAs6i_m1feFyqYV6WTswgfPbjpm_E843hQ |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEF5VqYS4IJ4iUGARUFGpVrz2Zu09oEJoo4ZCFFWt1JvZl5tKlR3iVCg3_gP_hp_DL-mMH0ktIW69WfZIXs9rZzyz3xDy1ti-ETrlXuxU6nFttKdt7HvWgGvUgTJpCV_8bSwOT_mXs_7ZBvnTnIXBtsrGJ5aO2uYG_5H3gggBdWH_F720bouY7A_3Zj88nCCFldZmnEalIkdu-RPSt-LDaB9k_S4Ihgcnnw-9esKAZziXC8-BeqtQc-67WPqwbgjihEL8FhMxpxG5UsdWxZoFkbPSt1g0TI2yAXPShQh6AO5_M4KsyO-QzcHBeHLc7AP9iHFWAaKGofR7sylCr0PGwFtbYDkpoBXetpszb-x2w_vkXh2m0k-VXj0gGy57SLYnFc71cpeerI9tFbt0m07WCNjLR-Tj4CJf3IiI84zmKX3_99fvHW9U4Mgwd55fUr2kx1NIi8Enm6uCzstrnBtUPCant8LIJ6ST5Zl7SqhTXEMMipkO40YYJawSoXaRstKKmHXJTsO9xNQ45jhO4zKBfAY5naw53SVvVrSzCr3jn1QDFMKKAhG3yxv5_DypDTjRIkp96Vhg4YsN-HnDbCR9oYwCv6d0l2w1IkxqN1Aka6Xtkterx2DAWJVRmQOGIg0WRyMmuyRqib61oPaT7GJaQoFLHB7uh8_-__JX5A7YSvJ1ND56Tu4GeIADm17CLdJZzK_cCwirFvplrb-UfL9tk7kGOsk7ug |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Biotransformation+of+%28%E2%80%93%29-Isopulegol+by+Rhodococcus+rhodochrous&rft.jtitle=Pharmaceuticals+%28Basel%2C+Switzerland%29&rft.au=Ivshina%2C+Irina+B.&rft.au=Luchnikova%2C+Natalia+A.&rft.au=Maltseva%2C+Polina+Yu&rft.au=Ilyina%2C+Irina+V.&rft.date=2022-08-03&rft.issn=1424-8247&rft.eissn=1424-8247&rft.volume=15&rft.issue=8&rft.spage=964&rft_id=info:doi/10.3390%2Fph15080964&rft.externalDBID=n%2Fa&rft.externalDocID=10_3390_ph15080964 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1424-8247&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1424-8247&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1424-8247&client=summon |