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Comparative Analysis of Water-Soluble Polysaccharides from Dendrobium Second Love 'Tokimeki' and Dendrobium nobile in Structure, Antioxidant, and Anti-Tumor Activity In Vitro
With potential anti-tumor and antioxidant properties, the polysaccharide content of is relatively lower than that of the other medicinal To find high-content polysaccharide resources, the polysaccharide (DHPP-Ⅰs) was prepared from Second Love 'Tokimeki' (a hybrid) and compared with DNPP-Ⅰs...
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Published in: | International journal of molecular sciences 2023-06, Vol.24 (12), p.10361 |
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creator | Ye, Guangying Zhang, Jinhui Xu, Xiaoli Zeng, Canbiao Ye, Qingsheng Wang, Zaihua |
description | With potential anti-tumor and antioxidant properties, the polysaccharide content of
is relatively lower than that of the other medicinal
To find high-content polysaccharide resources, the polysaccharide (DHPP-Ⅰs) was prepared from
Second Love 'Tokimeki' (a
hybrid) and compared with DNPP-Ⅰs from
. DHPP-Is (Mn 31.09 kDa) and DNPP-Is (Mn 46.65 kDa) were found to be
-acetylated glucomannans (-Glc
-(1,4) and
-acetylated-D-Man
-(1,4) backbones), analogous to other
polysaccharides. DHPP-Ⅰs had higher glucose content (31.1%) and a lower degree (0.16) of acetylation than DNPP-Ⅰs (15.8%, 0.28). Meanwhile, DHPP-Ⅰs and DNPP-Ⅰs had the same ability in the radical scavenging assay, which was milder than the control of Vc. Both DHPP-Is and DNPP-Is inhibited
cell proliferation in vitro, with obvious differences in dose concentrations (0.5-2.0 mg/mL) and treatment times (24-72 h). Therefore, the antioxidant activity of DHPP-Ⅰs and DNPP-Ⅰs is not associated with distinction in anti-proliferative activity. As a glucomannan derived from non-medicinal
, DHPP-Ⅰs has similar bioactivity to other medicinal
and this could serve as a starting point for studying the conformational-bioactivity relationship of
polysaccharides. |
doi_str_mv | 10.3390/ijms241210361 |
format | article |
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is relatively lower than that of the other medicinal
To find high-content polysaccharide resources, the polysaccharide (DHPP-Ⅰs) was prepared from
Second Love 'Tokimeki' (a
hybrid) and compared with DNPP-Ⅰs from
. DHPP-Is (Mn 31.09 kDa) and DNPP-Is (Mn 46.65 kDa) were found to be
-acetylated glucomannans (-Glc
-(1,4) and
-acetylated-D-Man
-(1,4) backbones), analogous to other
polysaccharides. DHPP-Ⅰs had higher glucose content (31.1%) and a lower degree (0.16) of acetylation than DNPP-Ⅰs (15.8%, 0.28). Meanwhile, DHPP-Ⅰs and DNPP-Ⅰs had the same ability in the radical scavenging assay, which was milder than the control of Vc. Both DHPP-Is and DNPP-Is inhibited
cell proliferation in vitro, with obvious differences in dose concentrations (0.5-2.0 mg/mL) and treatment times (24-72 h). Therefore, the antioxidant activity of DHPP-Ⅰs and DNPP-Ⅰs is not associated with distinction in anti-proliferative activity. As a glucomannan derived from non-medicinal
, DHPP-Ⅰs has similar bioactivity to other medicinal
and this could serve as a starting point for studying the conformational-bioactivity relationship of
polysaccharides.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms241210361</identifier><identifier>PMID: 37373508</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Acetylation ; anti-tumor activity ; antioxidant activity ; Antioxidants ; Antioxidants - pharmacology ; Biological activity ; Cell cycle ; Cell proliferation ; Chromatography ; Comparative analysis ; Dendrobium ; Dendrobium - chemistry ; Dendrobium nobile ; Dendrobium Second Love ‘Tokimeki’ ; Diabetes ; Glucose ; Love ; Molecular weight ; Neoplasms ; polysaccharide ; Polysaccharides ; Polysaccharides - chemistry ; Polysaccharides - pharmacology ; Scavenging ; Spectrum analysis ; Tumors ; Water - chemistry</subject><ispartof>International journal of molecular sciences, 2023-06, Vol.24 (12), p.10361</ispartof><rights>2023 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.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-b7ff343893d554a26cc2cce1297138a459b1eb9e0b86d7538e5f87a72cfc5b543</citedby><cites>FETCH-LOGICAL-c482t-b7ff343893d554a26cc2cce1297138a459b1eb9e0b86d7538e5f87a72cfc5b543</cites><orcidid>0000-0003-1744-0996</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2829821357/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2829821357?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37373508$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ye, Guangying</creatorcontrib><creatorcontrib>Zhang, Jinhui</creatorcontrib><creatorcontrib>Xu, Xiaoli</creatorcontrib><creatorcontrib>Zeng, Canbiao</creatorcontrib><creatorcontrib>Ye, Qingsheng</creatorcontrib><creatorcontrib>Wang, Zaihua</creatorcontrib><title>Comparative Analysis of Water-Soluble Polysaccharides from Dendrobium Second Love 'Tokimeki' and Dendrobium nobile in Structure, Antioxidant, and Anti-Tumor Activity In Vitro</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>With potential anti-tumor and antioxidant properties, the polysaccharide content of
is relatively lower than that of the other medicinal
To find high-content polysaccharide resources, the polysaccharide (DHPP-Ⅰs) was prepared from
Second Love 'Tokimeki' (a
hybrid) and compared with DNPP-Ⅰs from
. DHPP-Is (Mn 31.09 kDa) and DNPP-Is (Mn 46.65 kDa) were found to be
-acetylated glucomannans (-Glc
-(1,4) and
-acetylated-D-Man
-(1,4) backbones), analogous to other
polysaccharides. DHPP-Ⅰs had higher glucose content (31.1%) and a lower degree (0.16) of acetylation than DNPP-Ⅰs (15.8%, 0.28). Meanwhile, DHPP-Ⅰs and DNPP-Ⅰs had the same ability in the radical scavenging assay, which was milder than the control of Vc. Both DHPP-Is and DNPP-Is inhibited
cell proliferation in vitro, with obvious differences in dose concentrations (0.5-2.0 mg/mL) and treatment times (24-72 h). Therefore, the antioxidant activity of DHPP-Ⅰs and DNPP-Ⅰs is not associated with distinction in anti-proliferative activity. As a glucomannan derived from non-medicinal
, DHPP-Ⅰs has similar bioactivity to other medicinal
and this could serve as a starting point for studying the conformational-bioactivity relationship of
polysaccharides.</description><subject>Acetylation</subject><subject>anti-tumor activity</subject><subject>antioxidant activity</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Biological activity</subject><subject>Cell cycle</subject><subject>Cell proliferation</subject><subject>Chromatography</subject><subject>Comparative analysis</subject><subject>Dendrobium</subject><subject>Dendrobium - chemistry</subject><subject>Dendrobium nobile</subject><subject>Dendrobium Second Love ‘Tokimeki’</subject><subject>Diabetes</subject><subject>Glucose</subject><subject>Love</subject><subject>Molecular weight</subject><subject>Neoplasms</subject><subject>polysaccharide</subject><subject>Polysaccharides</subject><subject>Polysaccharides - chemistry</subject><subject>Polysaccharides - pharmacology</subject><subject>Scavenging</subject><subject>Spectrum analysis</subject><subject>Tumors</subject><subject>Water - chemistry</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkltv0zAUgCMEYqPwyCuyxMP2sAxf4sR5QlXHpVKlIbXAo-XYJ5u7JC62M9E_xW_EXcfUIls61jmfP9vyybK3BF8yVuMPdt0HWhBKMCvJs-yUFJTmGJfV84P1SfYqhDXGlFFev8xOWJUGx-I0-zNz_UZ5Fe09oOmgum2wAbkW_VQRfL503dh0gL65VFBa3ypvDQTUetejKxiMd40de7QE7QaDFi5ZzlbuzvZwZ8-QSrkDakghyeyAltGPOo4eLtKh0brf1qghXjxs2CXy1dg7j6Y63cvGLZoP6IeN3r3OXrSqC_DmMU6y758_rWZf88X1l_lsush1IWjMm6ptWcFEzQznhaKl1lRrILSuCBOq4HVDoKkBN6I0FWcCeCsqVVHdat7wgk2y-d5rnFrLjbe98lvplJUPCedvpPLR6g6kIJxgw5UWhhdlUrdVWWNdaFyUnINKro9712ZsejAahuhVdyQ9rgz2Vt64e0kwrWuW5iQ7fzR492uEEGVvg4auUwO4MUgqGC7LdDpN6Pv_0LUbffrXHUVrQQnjVaLyPaW9C8FD-3QbguWureRRWyX-3eETnuh_fcT-Am3nyxA</recordid><startdate>20230620</startdate><enddate>20230620</enddate><creator>Ye, Guangying</creator><creator>Zhang, Jinhui</creator><creator>Xu, Xiaoli</creator><creator>Zeng, Canbiao</creator><creator>Ye, Qingsheng</creator><creator>Wang, Zaihua</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1744-0996</orcidid></search><sort><creationdate>20230620</creationdate><title>Comparative Analysis of Water-Soluble Polysaccharides from Dendrobium Second Love 'Tokimeki' and Dendrobium nobile in Structure, Antioxidant, and Anti-Tumor Activity In Vitro</title><author>Ye, Guangying ; 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is relatively lower than that of the other medicinal
To find high-content polysaccharide resources, the polysaccharide (DHPP-Ⅰs) was prepared from
Second Love 'Tokimeki' (a
hybrid) and compared with DNPP-Ⅰs from
. DHPP-Is (Mn 31.09 kDa) and DNPP-Is (Mn 46.65 kDa) were found to be
-acetylated glucomannans (-Glc
-(1,4) and
-acetylated-D-Man
-(1,4) backbones), analogous to other
polysaccharides. DHPP-Ⅰs had higher glucose content (31.1%) and a lower degree (0.16) of acetylation than DNPP-Ⅰs (15.8%, 0.28). Meanwhile, DHPP-Ⅰs and DNPP-Ⅰs had the same ability in the radical scavenging assay, which was milder than the control of Vc. Both DHPP-Is and DNPP-Is inhibited
cell proliferation in vitro, with obvious differences in dose concentrations (0.5-2.0 mg/mL) and treatment times (24-72 h). Therefore, the antioxidant activity of DHPP-Ⅰs and DNPP-Ⅰs is not associated with distinction in anti-proliferative activity. As a glucomannan derived from non-medicinal
, DHPP-Ⅰs has similar bioactivity to other medicinal
and this could serve as a starting point for studying the conformational-bioactivity relationship of
polysaccharides.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37373508</pmid><doi>10.3390/ijms241210361</doi><orcidid>https://orcid.org/0000-0003-1744-0996</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetylation anti-tumor activity antioxidant activity Antioxidants Antioxidants - pharmacology Biological activity Cell cycle Cell proliferation Chromatography Comparative analysis Dendrobium Dendrobium - chemistry Dendrobium nobile Dendrobium Second Love ‘Tokimeki’ Diabetes Glucose Love Molecular weight Neoplasms polysaccharide Polysaccharides Polysaccharides - chemistry Polysaccharides - pharmacology Scavenging Spectrum analysis Tumors Water - chemistry |
title | Comparative Analysis of Water-Soluble Polysaccharides from Dendrobium Second Love 'Tokimeki' and Dendrobium nobile in Structure, Antioxidant, and Anti-Tumor Activity In Vitro |
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