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Multifunctional alkalophilic α-amylase with diverse raw seaweed degrading activities
Uncultured microbes are an important resource for the discovery of novel enzymes. In this study, an amylase gene ( amy2587 ) that codes a protein with 587 amino acids (Amy2587) was obtained from the metagenomic library of macroalgae-associated bacteria. Recombinant Amy2587 was expressed in Escherich...
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Published in: | AMB Express 2021-10, Vol.11 (1), p.139-139, Article 139 |
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description | Uncultured microbes are an important resource for the discovery of novel enzymes. In this study, an amylase gene (
amy2587
) that codes a protein with 587 amino acids (Amy2587) was obtained from the metagenomic library of macroalgae-associated bacteria. Recombinant Amy2587 was expressed in
Escherichia coli
BL21 (DE3) and was found to simultaneously possess α-amylase, agarase, carrageenase, cellulase, and alginate lyase activities. Moreover, recombinant Amy2587 showed high thermostability and alkali resistance which are important characteristics for industrial application. To investigate the multifunctional mechanism of Amy2587, three motifs (functional domains) in the Amy2587 sequence were deleted to generate three truncated Amy2587 variants. The results showed that, even though these functional domains affected the multiple substrates degrading activity of Amy2587, they did not wholly explain its multifunctional characteristics. To apply the multifunctional activity of Amy2587, three seaweed substrates (
Grateloupia filicina, Chondrus ocellatus
, and
Scagassum
) were digested using Amy2587. After 2 h, 6 h, and 24 h of digestion, 121.2 ± 4 µg/ml, 134.8 ± 6 µg/ml, and 70.3 ± 3.5 µg/ml of reducing sugars were released, respectively. These results show that Amy2587 directly and effectively degraded three kinds of raw seaweeds. This finding provides a theoretical basis for one-step enzymatic digestion of raw seaweeds to obtain seaweed oligosaccharides. |
doi_str_mv | 10.1186/s13568-021-01300-x |
format | article |
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amy2587
) that codes a protein with 587 amino acids (Amy2587) was obtained from the metagenomic library of macroalgae-associated bacteria. Recombinant Amy2587 was expressed in
Escherichia coli
BL21 (DE3) and was found to simultaneously possess α-amylase, agarase, carrageenase, cellulase, and alginate lyase activities. Moreover, recombinant Amy2587 showed high thermostability and alkali resistance which are important characteristics for industrial application. To investigate the multifunctional mechanism of Amy2587, three motifs (functional domains) in the Amy2587 sequence were deleted to generate three truncated Amy2587 variants. The results showed that, even though these functional domains affected the multiple substrates degrading activity of Amy2587, they did not wholly explain its multifunctional characteristics. To apply the multifunctional activity of Amy2587, three seaweed substrates (
Grateloupia filicina, Chondrus ocellatus
, and
Scagassum
) were digested using Amy2587. After 2 h, 6 h, and 24 h of digestion, 121.2 ± 4 µg/ml, 134.8 ± 6 µg/ml, and 70.3 ± 3.5 µg/ml of reducing sugars were released, respectively. These results show that Amy2587 directly and effectively degraded three kinds of raw seaweeds. This finding provides a theoretical basis for one-step enzymatic digestion of raw seaweeds to obtain seaweed oligosaccharides.</description><identifier>ISSN: 2191-0855</identifier><identifier>EISSN: 2191-0855</identifier><identifier>DOI: 10.1186/s13568-021-01300-x</identifier><identifier>PMID: 34669086</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Agarase ; Algae ; Alginate lyase ; Alginates ; Alginic acid ; Amino acids ; Amylases ; Biomedical and Life Sciences ; Biotechnology ; Cellulase ; Coliforms ; Degradation ; Digestion ; Domains ; E coli ; Enzymatic digestion ; Industrial applications ; Life Sciences ; Metagenomic ; Metagenomics ; Microbial Genetics and Genomics ; Microbiology ; Multifunctional enzyme ; Oligosaccharides ; Original ; Original Article ; Seaweeds ; Substrates ; Sugar ; Thermal stability ; α-Amylase</subject><ispartof>AMB Express, 2021-10, Vol.11 (1), p.139-139, Article 139</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-d0df3f4aa890b390c16593f0634a21fb30934335ce3334b95add50f698495d133</citedby><cites>FETCH-LOGICAL-c517t-d0df3f4aa890b390c16593f0634a21fb30934335ce3334b95add50f698495d133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2583708745/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2583708745?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids></links><search><creatorcontrib>Gu, Xiaoqian</creatorcontrib><creatorcontrib>Fu, Liping</creatorcontrib><creatorcontrib>Pan, Aihong</creatorcontrib><creatorcontrib>Gui, Yuanyuan</creatorcontrib><creatorcontrib>Zhang, Qian</creatorcontrib><creatorcontrib>Li, Jiang</creatorcontrib><title>Multifunctional alkalophilic α-amylase with diverse raw seaweed degrading activities</title><title>AMB Express</title><addtitle>AMB Expr</addtitle><description>Uncultured microbes are an important resource for the discovery of novel enzymes. In this study, an amylase gene (
amy2587
) that codes a protein with 587 amino acids (Amy2587) was obtained from the metagenomic library of macroalgae-associated bacteria. Recombinant Amy2587 was expressed in
Escherichia coli
BL21 (DE3) and was found to simultaneously possess α-amylase, agarase, carrageenase, cellulase, and alginate lyase activities. Moreover, recombinant Amy2587 showed high thermostability and alkali resistance which are important characteristics for industrial application. To investigate the multifunctional mechanism of Amy2587, three motifs (functional domains) in the Amy2587 sequence were deleted to generate three truncated Amy2587 variants. The results showed that, even though these functional domains affected the multiple substrates degrading activity of Amy2587, they did not wholly explain its multifunctional characteristics. To apply the multifunctional activity of Amy2587, three seaweed substrates (
Grateloupia filicina, Chondrus ocellatus
, and
Scagassum
) were digested using Amy2587. After 2 h, 6 h, and 24 h of digestion, 121.2 ± 4 µg/ml, 134.8 ± 6 µg/ml, and 70.3 ± 3.5 µg/ml of reducing sugars were released, respectively. These results show that Amy2587 directly and effectively degraded three kinds of raw seaweeds. This finding provides a theoretical basis for one-step enzymatic digestion of raw seaweeds to obtain seaweed oligosaccharides.</description><subject>Agarase</subject><subject>Algae</subject><subject>Alginate lyase</subject><subject>Alginates</subject><subject>Alginic acid</subject><subject>Amino acids</subject><subject>Amylases</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Cellulase</subject><subject>Coliforms</subject><subject>Degradation</subject><subject>Digestion</subject><subject>Domains</subject><subject>E coli</subject><subject>Enzymatic digestion</subject><subject>Industrial applications</subject><subject>Life Sciences</subject><subject>Metagenomic</subject><subject>Metagenomics</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>Multifunctional enzyme</subject><subject>Oligosaccharides</subject><subject>Original</subject><subject>Original Article</subject><subject>Seaweeds</subject><subject>Substrates</subject><subject>Sugar</subject><subject>Thermal stability</subject><subject>α-Amylase</subject><issn>2191-0855</issn><issn>2191-0855</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9ks1uEzEUhS0EolXoC7AaiQ2bAXv8E3uDhCoKlYrY0LV145-JgzMO9kzSPhYvwjPhZCqgLPDGvvY5372yDkIvCX5DiBRvC6FcyBZ3pMWEYtzePUHnHVG1lJw__et8hi5K2eC6OMZK8OfojDIhFJbiHN1-nuIY_DSYMaQBYgPxG8S0W4cYTPPzRwvb-wjFNYcwrhsb9i7XIsOhKQ4OztnGuj6DDUPfQGXswxhceYGeeYjFXTzsC3R79eHr5af25svH68v3N63hZDm2FltPPQOQCq-owoYIrqjHgjLoiF9RrCijlBtHKWUrxcFajr1QkiluCaULdD1zbYKN3uWwhXyvEwR9uki515DHYKLTnfNeLblaKjCMKyaVMNw503W4EmvbBXo3s3bTauusccOYIT6CPn4Zwlr3aa8l7-r8R8DrB0BO3ydXRr0NxbgYYXBpKrrjkmHCCD7O_eof6SZNuX7_SUWXWC4Zr6puVpmcSsnO_x6GYH0MgZ5DoGsI9CkE-q6a6GwqVTz0Lv9B_8f1C5ettEU</recordid><startdate>20211020</startdate><enddate>20211020</enddate><creator>Gu, Xiaoqian</creator><creator>Fu, Liping</creator><creator>Pan, Aihong</creator><creator>Gui, Yuanyuan</creator><creator>Zhang, Qian</creator><creator>Li, Jiang</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><general>SpringerOpen</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>LK8</scope><scope>M7P</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20211020</creationdate><title>Multifunctional alkalophilic α-amylase with diverse raw seaweed degrading activities</title><author>Gu, Xiaoqian ; Fu, Liping ; Pan, Aihong ; Gui, Yuanyuan ; Zhang, Qian ; Li, Jiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-d0df3f4aa890b390c16593f0634a21fb30934335ce3334b95add50f698495d133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Agarase</topic><topic>Algae</topic><topic>Alginate lyase</topic><topic>Alginates</topic><topic>Alginic acid</topic><topic>Amino acids</topic><topic>Amylases</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Cellulase</topic><topic>Coliforms</topic><topic>Degradation</topic><topic>Digestion</topic><topic>Domains</topic><topic>E coli</topic><topic>Enzymatic digestion</topic><topic>Industrial applications</topic><topic>Life Sciences</topic><topic>Metagenomic</topic><topic>Metagenomics</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiology</topic><topic>Multifunctional enzyme</topic><topic>Oligosaccharides</topic><topic>Original</topic><topic>Original Article</topic><topic>Seaweeds</topic><topic>Substrates</topic><topic>Sugar</topic><topic>Thermal stability</topic><topic>α-Amylase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gu, Xiaoqian</creatorcontrib><creatorcontrib>Fu, Liping</creatorcontrib><creatorcontrib>Pan, Aihong</creatorcontrib><creatorcontrib>Gui, Yuanyuan</creatorcontrib><creatorcontrib>Zhang, Qian</creatorcontrib><creatorcontrib>Li, Jiang</creatorcontrib><collection>SpringerOpen</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>AMB Express</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gu, Xiaoqian</au><au>Fu, Liping</au><au>Pan, Aihong</au><au>Gui, Yuanyuan</au><au>Zhang, Qian</au><au>Li, Jiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multifunctional alkalophilic α-amylase with diverse raw seaweed degrading activities</atitle><jtitle>AMB Express</jtitle><stitle>AMB Expr</stitle><date>2021-10-20</date><risdate>2021</risdate><volume>11</volume><issue>1</issue><spage>139</spage><epage>139</epage><pages>139-139</pages><artnum>139</artnum><issn>2191-0855</issn><eissn>2191-0855</eissn><abstract>Uncultured microbes are an important resource for the discovery of novel enzymes. In this study, an amylase gene (
amy2587
) that codes a protein with 587 amino acids (Amy2587) was obtained from the metagenomic library of macroalgae-associated bacteria. Recombinant Amy2587 was expressed in
Escherichia coli
BL21 (DE3) and was found to simultaneously possess α-amylase, agarase, carrageenase, cellulase, and alginate lyase activities. Moreover, recombinant Amy2587 showed high thermostability and alkali resistance which are important characteristics for industrial application. To investigate the multifunctional mechanism of Amy2587, three motifs (functional domains) in the Amy2587 sequence were deleted to generate three truncated Amy2587 variants. The results showed that, even though these functional domains affected the multiple substrates degrading activity of Amy2587, they did not wholly explain its multifunctional characteristics. To apply the multifunctional activity of Amy2587, three seaweed substrates (
Grateloupia filicina, Chondrus ocellatus
, and
Scagassum
) were digested using Amy2587. After 2 h, 6 h, and 24 h of digestion, 121.2 ± 4 µg/ml, 134.8 ± 6 µg/ml, and 70.3 ± 3.5 µg/ml of reducing sugars were released, respectively. These results show that Amy2587 directly and effectively degraded three kinds of raw seaweeds. This finding provides a theoretical basis for one-step enzymatic digestion of raw seaweeds to obtain seaweed oligosaccharides.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>34669086</pmid><doi>10.1186/s13568-021-01300-x</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Agarase Algae Alginate lyase Alginates Alginic acid Amino acids Amylases Biomedical and Life Sciences Biotechnology Cellulase Coliforms Degradation Digestion Domains E coli Enzymatic digestion Industrial applications Life Sciences Metagenomic Metagenomics Microbial Genetics and Genomics Microbiology Multifunctional enzyme Oligosaccharides Original Original Article Seaweeds Substrates Sugar Thermal stability α-Amylase |
title | Multifunctional alkalophilic α-amylase with diverse raw seaweed degrading activities |
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