A highly branched glucomannan from the fruiting body of Schizophyllum commune: Structural characteristics and antitumor properties analysis

In this study, a highly branched glucomannan (SCP-1) from Schizophyllum commune fruiting body with good solubility was isolated, and its structural characteristics and antitumor properties were analyzed. The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mann...

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Veröffentlicht in:International journal of biological macromolecules 2024-12, Vol.282 (Pt 6), p.137460, Article 137460
Hauptverfasser: Gao, Hong, Shi, Defang, Yin, Chaomin, Fan, Xiuzhi, Cheng, Xianbo, Qiao, Xin, Liu, Chunyou, Hu, Guoyuan, Yao, Fen, Qiu, Jianhui, Yu, Wei
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container_issue Pt 6
container_start_page 137460
container_title International journal of biological macromolecules
container_volume 282
creator Gao, Hong
Shi, Defang
Yin, Chaomin
Fan, Xiuzhi
Cheng, Xianbo
Qiao, Xin
Liu, Chunyou
Hu, Guoyuan
Yao, Fen
Qiu, Jianhui
Yu, Wei
description In this study, a highly branched glucomannan (SCP-1) from Schizophyllum commune fruiting body with good solubility was isolated, and its structural characteristics and antitumor properties were analyzed. The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mannose with a relative molar ratio of 14:6:210:593:177, and the molecular weight (Mw) of SCP-1 was 15.1 kDa. SCP-1 showed a rough and dense surface, and it was aggregated to particles in distilled water, though it might have triple-helix conformation. The main backbone chain of SCP-1 was →[3)-β-D-Glcp-(1]3→3)-β-D-Glcp-(1→2)-α-D-Manp-(1→2)-α-D-Manp-(1→3)-α-D-Glcp-(1→ and three sides chains including α-D-Glcp-(1→[6)-β-D-Glcp-(1]2→, α-D-Glcp-(1→3)-α-D-Manp-(1→ and α-D-Glcp-(1→[6)-α-D-Galp-(1]3→ were linked with 1,6-glycosidic bond, which was significantly different with the schizophyllan isolated from the mycelia of S. commune. SCP-1 could significantly inhibit the growth of A549 cells, the inhibition rate reached 41.62 % and the percentage of cells in S phase increased from 27.17 % to 56.40 % (400 μg/mL, 48 h). Moreover, SCP-1 could induce cell apoptosis and the total apoptosis rate reached 28.13 %. SCP-1 exerted apoptosis inducing effect probably by reducing the expression ratio of Bcl-2/Bax and the p-PI3K, p-Akt and p-mTOR expression level. The results showed that SCP-1 might have the potential to act as an antitumor agent for lung cancer therapy. •A highly branched glucomannan from the artificially cultivated S. commune were purified.•The structure of SCP-1 contained a main backbone and three sides chains.•SCP-1 structure was significantly different with schizophyllan that previously reported.•SCP-1 significantly inhibited the growth of A549 cells and arrested the cell cycle in S phase.•The cell apoptosis induced by SCP-1 might via inhibition of PI3K/Akt/mTOR signaling pathway.
doi_str_mv 10.1016/j.ijbiomac.2024.137460
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The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mannose with a relative molar ratio of 14:6:210:593:177, and the molecular weight (Mw) of SCP-1 was 15.1 kDa. SCP-1 showed a rough and dense surface, and it was aggregated to particles in distilled water, though it might have triple-helix conformation. The main backbone chain of SCP-1 was →[3)-β-D-Glcp-(1]3→3)-β-D-Glcp-(1→2)-α-D-Manp-(1→2)-α-D-Manp-(1→3)-α-D-Glcp-(1→ and three sides chains including α-D-Glcp-(1→[6)-β-D-Glcp-(1]2→, α-D-Glcp-(1→3)-α-D-Manp-(1→ and α-D-Glcp-(1→[6)-α-D-Galp-(1]3→ were linked with 1,6-glycosidic bond, which was significantly different with the schizophyllan isolated from the mycelia of S. commune. SCP-1 could significantly inhibit the growth of A549 cells, the inhibition rate reached 41.62 % and the percentage of cells in S phase increased from 27.17 % to 56.40 % (400 μg/mL, 48 h). Moreover, SCP-1 could induce cell apoptosis and the total apoptosis rate reached 28.13 %. SCP-1 exerted apoptosis inducing effect probably by reducing the expression ratio of Bcl-2/Bax and the p-PI3K, p-Akt and p-mTOR expression level. The results showed that SCP-1 might have the potential to act as an antitumor agent for lung cancer therapy. •A highly branched glucomannan from the artificially cultivated S. commune were purified.•The structure of SCP-1 contained a main backbone and three sides chains.•SCP-1 structure was significantly different with schizophyllan that previously reported.•SCP-1 significantly inhibited the growth of A549 cells and arrested the cell cycle in S phase.•The cell apoptosis induced by SCP-1 might via inhibition of PI3K/Akt/mTOR signaling pathway.</description><identifier>ISSN: 0141-8130</identifier><identifier>ISSN: 1879-0003</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2024.137460</identifier><identifier>PMID: 39528189</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>A549 Cells ; antineoplastic agents ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - isolation &amp; purification ; Antineoplastic Agents - pharmacology ; Antitumor activity ; apoptosis ; Apoptosis - drug effects ; Apoptosis induction ; cancer therapy ; Cell Line, Tumor ; Fruiting Bodies, Fungal - chemistry ; fucose ; galactose ; Glucomannan ; glucomannans ; glucosamine ; glucose ; Humans ; interphase ; lung neoplasms ; Mannans - chemistry ; Mannans - isolation &amp; purification ; Mannans - pharmacology ; mannose ; Molecular Weight ; Monosaccharides - analysis ; Monosaccharides - chemistry ; mycelium ; schizophyllan ; Schizophyllum - chemistry ; Schizophyllum commune ; solubility ; Structural characterization</subject><ispartof>International journal of biological macromolecules, 2024-12, Vol.282 (Pt 6), p.137460, Article 137460</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. 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The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mannose with a relative molar ratio of 14:6:210:593:177, and the molecular weight (Mw) of SCP-1 was 15.1 kDa. SCP-1 showed a rough and dense surface, and it was aggregated to particles in distilled water, though it might have triple-helix conformation. The main backbone chain of SCP-1 was →[3)-β-D-Glcp-(1]3→3)-β-D-Glcp-(1→2)-α-D-Manp-(1→2)-α-D-Manp-(1→3)-α-D-Glcp-(1→ and three sides chains including α-D-Glcp-(1→[6)-β-D-Glcp-(1]2→, α-D-Glcp-(1→3)-α-D-Manp-(1→ and α-D-Glcp-(1→[6)-α-D-Galp-(1]3→ were linked with 1,6-glycosidic bond, which was significantly different with the schizophyllan isolated from the mycelia of S. commune. SCP-1 could significantly inhibit the growth of A549 cells, the inhibition rate reached 41.62 % and the percentage of cells in S phase increased from 27.17 % to 56.40 % (400 μg/mL, 48 h). Moreover, SCP-1 could induce cell apoptosis and the total apoptosis rate reached 28.13 %. SCP-1 exerted apoptosis inducing effect probably by reducing the expression ratio of Bcl-2/Bax and the p-PI3K, p-Akt and p-mTOR expression level. The results showed that SCP-1 might have the potential to act as an antitumor agent for lung cancer therapy. •A highly branched glucomannan from the artificially cultivated S. commune were purified.•The structure of SCP-1 contained a main backbone and three sides chains.•SCP-1 structure was significantly different with schizophyllan that previously reported.•SCP-1 significantly inhibited the growth of A549 cells and arrested the cell cycle in S phase.•The cell apoptosis induced by SCP-1 might via inhibition of PI3K/Akt/mTOR signaling pathway.</description><subject>A549 Cells</subject><subject>antineoplastic agents</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - isolation &amp; purification</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antitumor activity</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis induction</subject><subject>cancer therapy</subject><subject>Cell Line, Tumor</subject><subject>Fruiting Bodies, Fungal - chemistry</subject><subject>fucose</subject><subject>galactose</subject><subject>Glucomannan</subject><subject>glucomannans</subject><subject>glucosamine</subject><subject>glucose</subject><subject>Humans</subject><subject>interphase</subject><subject>lung neoplasms</subject><subject>Mannans - chemistry</subject><subject>Mannans - isolation &amp; purification</subject><subject>Mannans - pharmacology</subject><subject>mannose</subject><subject>Molecular Weight</subject><subject>Monosaccharides - analysis</subject><subject>Monosaccharides - chemistry</subject><subject>mycelium</subject><subject>schizophyllan</subject><subject>Schizophyllum - chemistry</subject><subject>Schizophyllum commune</subject><subject>solubility</subject><subject>Structural characterization</subject><issn>0141-8130</issn><issn>1879-0003</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u3CAUhVHVqJkmfYWIZTeegG0M7qpRlP5IkbpIskYYLmNGtpnyU8l5hb50GU3Sbbu44urynXsQB6ErSraU0O56v3X7wflZ6W1N6nZLG9525A3aUMH7ihDSvEUbQltaCdqQc_Q-xn2ZdoyKd-i86VktqOg36PcNHt1unFY8BLXoEQzeTVmXxcuiFmyDn3EaoTTZJbfs8ODNir3FD3p0z_4wrtOUZ1wEc17gE35IIeuUg5qwHlVQOkFwMTkdsVpMqeRSnn3Ah-APEJKD44Wa1ujiJTqzaorw4eW8QE9f7h5vv1X3P75-v725r3TNRaqUZcTUBDoxGK5401utDGWUDsa2ZjBsEC230FKjOe8NU7UxxvZUCKENUU1zgT6e9pY3_MwQk5xd1DBNagGfo2woa-uuZaL-D7QWnBUbVtDuhOrgYwxg5SG4WYVVUiKPmcm9fM1MHjOTp8yK8OrFIw8zmL-y15AK8PkEQPmUXw6CjNrBosG4ADpJ492_PP4AEzCv8Q</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Gao, Hong</creator><creator>Shi, Defang</creator><creator>Yin, Chaomin</creator><creator>Fan, Xiuzhi</creator><creator>Cheng, Xianbo</creator><creator>Qiao, Xin</creator><creator>Liu, Chunyou</creator><creator>Hu, Guoyuan</creator><creator>Yao, Fen</creator><creator>Qiu, Jianhui</creator><creator>Yu, Wei</creator><general>Elsevier B.V</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>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202412</creationdate><title>A highly branched glucomannan from the fruiting body of Schizophyllum commune: Structural characteristics and antitumor properties analysis</title><author>Gao, Hong ; 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purification</topic><topic>Mannans - pharmacology</topic><topic>mannose</topic><topic>Molecular Weight</topic><topic>Monosaccharides - analysis</topic><topic>Monosaccharides - chemistry</topic><topic>mycelium</topic><topic>schizophyllan</topic><topic>Schizophyllum - chemistry</topic><topic>Schizophyllum commune</topic><topic>solubility</topic><topic>Structural characterization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Hong</creatorcontrib><creatorcontrib>Shi, Defang</creatorcontrib><creatorcontrib>Yin, Chaomin</creatorcontrib><creatorcontrib>Fan, Xiuzhi</creatorcontrib><creatorcontrib>Cheng, Xianbo</creatorcontrib><creatorcontrib>Qiao, Xin</creatorcontrib><creatorcontrib>Liu, Chunyou</creatorcontrib><creatorcontrib>Hu, Guoyuan</creatorcontrib><creatorcontrib>Yao, Fen</creatorcontrib><creatorcontrib>Qiu, Jianhui</creatorcontrib><creatorcontrib>Yu, Wei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Hong</au><au>Shi, Defang</au><au>Yin, Chaomin</au><au>Fan, Xiuzhi</au><au>Cheng, Xianbo</au><au>Qiao, Xin</au><au>Liu, Chunyou</au><au>Hu, Guoyuan</au><au>Yao, Fen</au><au>Qiu, Jianhui</au><au>Yu, Wei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A highly branched glucomannan from the fruiting body of Schizophyllum commune: Structural characteristics and antitumor properties analysis</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-12</date><risdate>2024</risdate><volume>282</volume><issue>Pt 6</issue><spage>137460</spage><pages>137460-</pages><artnum>137460</artnum><issn>0141-8130</issn><issn>1879-0003</issn><eissn>1879-0003</eissn><abstract>In this study, a highly branched glucomannan (SCP-1) from Schizophyllum commune fruiting body with good solubility was isolated, and its structural characteristics and antitumor properties were analyzed. The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mannose with a relative molar ratio of 14:6:210:593:177, and the molecular weight (Mw) of SCP-1 was 15.1 kDa. SCP-1 showed a rough and dense surface, and it was aggregated to particles in distilled water, though it might have triple-helix conformation. The main backbone chain of SCP-1 was →[3)-β-D-Glcp-(1]3→3)-β-D-Glcp-(1→2)-α-D-Manp-(1→2)-α-D-Manp-(1→3)-α-D-Glcp-(1→ and three sides chains including α-D-Glcp-(1→[6)-β-D-Glcp-(1]2→, α-D-Glcp-(1→3)-α-D-Manp-(1→ and α-D-Glcp-(1→[6)-α-D-Galp-(1]3→ were linked with 1,6-glycosidic bond, which was significantly different with the schizophyllan isolated from the mycelia of S. commune. SCP-1 could significantly inhibit the growth of A549 cells, the inhibition rate reached 41.62 % and the percentage of cells in S phase increased from 27.17 % to 56.40 % (400 μg/mL, 48 h). Moreover, SCP-1 could induce cell apoptosis and the total apoptosis rate reached 28.13 %. SCP-1 exerted apoptosis inducing effect probably by reducing the expression ratio of Bcl-2/Bax and the p-PI3K, p-Akt and p-mTOR expression level. The results showed that SCP-1 might have the potential to act as an antitumor agent for lung cancer therapy. •A highly branched glucomannan from the artificially cultivated S. commune were purified.•The structure of SCP-1 contained a main backbone and three sides chains.•SCP-1 structure was significantly different with schizophyllan that previously reported.•SCP-1 significantly inhibited the growth of A549 cells and arrested the cell cycle in S phase.•The cell apoptosis induced by SCP-1 might via inhibition of PI3K/Akt/mTOR signaling pathway.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39528189</pmid><doi>10.1016/j.ijbiomac.2024.137460</doi></addata></record>
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subjects A549 Cells
antineoplastic agents
Antineoplastic Agents - chemistry
Antineoplastic Agents - isolation & purification
Antineoplastic Agents - pharmacology
Antitumor activity
apoptosis
Apoptosis - drug effects
Apoptosis induction
cancer therapy
Cell Line, Tumor
Fruiting Bodies, Fungal - chemistry
fucose
galactose
Glucomannan
glucomannans
glucosamine
glucose
Humans
interphase
lung neoplasms
Mannans - chemistry
Mannans - isolation & purification
Mannans - pharmacology
mannose
Molecular Weight
Monosaccharides - analysis
Monosaccharides - chemistry
mycelium
schizophyllan
Schizophyllum - chemistry
Schizophyllum commune
solubility
Structural characterization
title A highly branched glucomannan from the fruiting body of Schizophyllum commune: Structural characteristics and antitumor properties analysis
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