Laboratory‐scale preparation of prostaglandins using acetone powder of the red alga Gracilaria vermiculophylla
Summary The red alga Gracilaria vermiculophylla is a prostaglandin (PG)‐producing macroalga. The alga is rich in polyunsaturated fatty acids with 20 carbon atoms, mainly arachidonic acid (AA), which is a precursor of PGs. The purpose of the present study was to analyze the ability of the red alga to...
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creator | Illijas, Muhammad Ikbal Suzuki, Nobuya Honda, Masaki Arma, Nur Rahmawaty Nasir, Andriani Saleh, Luqman Dahlia, Dahlia Mulyani, Rahmi Itabashi, Yutaka |
description | Summary
The red alga Gracilaria vermiculophylla is a prostaglandin (PG)‐producing macroalga. The alga is rich in polyunsaturated fatty acids with 20 carbon atoms, mainly arachidonic acid (AA), which is a precursor of PGs. The purpose of the present study was to analyze the ability of the red alga to produce PGs using acetone powder as the crude enzyme prepared from the alga. The acetone powder (250 mg) was incubated with different amounts of exogenous AA (0.1–4 mg). For the determination of PG contents, 5 μL of a sample solution (5 mL in water) consisting of acetone powder and AA was injected into the HPLC column. For PG analysis, an HPLC system connected with a mass spectrometer was used. Results of the study showed that the released PGs from incubation of acetone powder and AA consisted of PGE2, 15‐keto‐PGE2, 15‐hydroperoxy‐PGE2, PGA2, and PGF2α. The capability of the crude enzyme prepared from the red alga to produce PGs was affected by available oxygen and AA concentrations. The crude enzyme (250 mg) was capable of producing 164 and 141 μg of PGE2 and 15‐keto‐PGE2, respectively, from incubation with 250 μg of AA. This in vitro method could be a simple way to provide PGs in the laboratory. |
doi_str_mv | 10.1111/pre.12548 |
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The red alga Gracilaria vermiculophylla is a prostaglandin (PG)‐producing macroalga. The alga is rich in polyunsaturated fatty acids with 20 carbon atoms, mainly arachidonic acid (AA), which is a precursor of PGs. The purpose of the present study was to analyze the ability of the red alga to produce PGs using acetone powder as the crude enzyme prepared from the alga. The acetone powder (250 mg) was incubated with different amounts of exogenous AA (0.1–4 mg). For the determination of PG contents, 5 μL of a sample solution (5 mL in water) consisting of acetone powder and AA was injected into the HPLC column. For PG analysis, an HPLC system connected with a mass spectrometer was used. Results of the study showed that the released PGs from incubation of acetone powder and AA consisted of PGE2, 15‐keto‐PGE2, 15‐hydroperoxy‐PGE2, PGA2, and PGF2α. The capability of the crude enzyme prepared from the red alga to produce PGs was affected by available oxygen and AA concentrations. The crude enzyme (250 mg) was capable of producing 164 and 141 μg of PGE2 and 15‐keto‐PGE2, respectively, from incubation with 250 μg of AA. This in vitro method could be a simple way to provide PGs in the laboratory.</description><identifier>ISSN: 1322-0829</identifier><identifier>EISSN: 1440-1835</identifier><identifier>DOI: 10.1111/pre.12548</identifier><language>eng</language><publisher>Kyoto, Japan: John Wiley & Sons Australia, Ltd</publisher><subject>15‐hydroperoxy‐PGE2 ; 15‐keto‐PGE2 ; Acetone ; Algae ; Arachidonic acid ; crude enzyme ; Enzymes ; Fatty acids ; Gracilaria vermiculophylla ; High-performance liquid chromatography ; HPLC ; In vitro methods and tests ; Incubation ; Liquid chromatography ; LS‐MS ; PGA2 ; PGE2 ; PGF2α ; Polyunsaturated fatty acids ; Powder ; Prostaglandin E2 ; Prostaglandins</subject><ispartof>Phycological research, 2024-07, Vol.72 (3), p.159-166</ispartof><rights>2024 Japanese Society of Phycology.</rights><rights>2024 Japanese Society of Phycology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2578-4d312c884aee59a87d97f2319d99752e6d8c029de8b3cddd2e39307526581a943</cites><orcidid>0000-0002-6216-7784</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpre.12548$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpre.12548$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids></links><search><creatorcontrib>Illijas, Muhammad Ikbal</creatorcontrib><creatorcontrib>Suzuki, Nobuya</creatorcontrib><creatorcontrib>Honda, Masaki</creatorcontrib><creatorcontrib>Arma, Nur Rahmawaty</creatorcontrib><creatorcontrib>Nasir, Andriani</creatorcontrib><creatorcontrib>Saleh, Luqman</creatorcontrib><creatorcontrib>Dahlia, Dahlia</creatorcontrib><creatorcontrib>Mulyani, Rahmi</creatorcontrib><creatorcontrib>Itabashi, Yutaka</creatorcontrib><title>Laboratory‐scale preparation of prostaglandins using acetone powder of the red alga Gracilaria vermiculophylla</title><title>Phycological research</title><description>Summary
The red alga Gracilaria vermiculophylla is a prostaglandin (PG)‐producing macroalga. The alga is rich in polyunsaturated fatty acids with 20 carbon atoms, mainly arachidonic acid (AA), which is a precursor of PGs. The purpose of the present study was to analyze the ability of the red alga to produce PGs using acetone powder as the crude enzyme prepared from the alga. The acetone powder (250 mg) was incubated with different amounts of exogenous AA (0.1–4 mg). For the determination of PG contents, 5 μL of a sample solution (5 mL in water) consisting of acetone powder and AA was injected into the HPLC column. For PG analysis, an HPLC system connected with a mass spectrometer was used. Results of the study showed that the released PGs from incubation of acetone powder and AA consisted of PGE2, 15‐keto‐PGE2, 15‐hydroperoxy‐PGE2, PGA2, and PGF2α. The capability of the crude enzyme prepared from the red alga to produce PGs was affected by available oxygen and AA concentrations. The crude enzyme (250 mg) was capable of producing 164 and 141 μg of PGE2 and 15‐keto‐PGE2, respectively, from incubation with 250 μg of AA. This in vitro method could be a simple way to provide PGs in the laboratory.</description><subject>15‐hydroperoxy‐PGE2</subject><subject>15‐keto‐PGE2</subject><subject>Acetone</subject><subject>Algae</subject><subject>Arachidonic acid</subject><subject>crude enzyme</subject><subject>Enzymes</subject><subject>Fatty acids</subject><subject>Gracilaria vermiculophylla</subject><subject>High-performance liquid chromatography</subject><subject>HPLC</subject><subject>In vitro methods and tests</subject><subject>Incubation</subject><subject>Liquid chromatography</subject><subject>LS‐MS</subject><subject>PGA2</subject><subject>PGE2</subject><subject>PGF2α</subject><subject>Polyunsaturated fatty acids</subject><subject>Powder</subject><subject>Prostaglandin E2</subject><subject>Prostaglandins</subject><issn>1322-0829</issn><issn>1440-1835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kL1OwzAQgC0EEqUw8AaRmBjS2k7S2COqSkGqBEIwR1f70qZy42AnVNl4BJ6RJ8ElrNxyf9_9EnLN6IQFmTYOJ4xnqTghI5amNGYiyU6DnXAeU8HlObnwfkcp5ZmQI9KsYG0dtNb1359fXoHBKPRoIMQqW0e2DK71LWwM1LqqfdT5qt5EoLC1dWDtQaM7Yu0WI4c6ArOBaOlAVQZcBdEHun2lOmObbW8MXJKzEozHqz89Jm_3i9f5Q7x6Wj7O71ax4lku4lQnjCshUkDMJIhcy7zkCZNayjzjONNCUS41inWitNYcE5nQkJllgoFMkzG5GfqG9d879G2xs52rw8gicIKllNM8ULcDpcKR3mFZNK7ag-sLRovjQ4OPxe9DAzsd2ENlsP8fLJ5fFkPFD2u8eew</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Illijas, Muhammad Ikbal</creator><creator>Suzuki, Nobuya</creator><creator>Honda, Masaki</creator><creator>Arma, Nur Rahmawaty</creator><creator>Nasir, Andriani</creator><creator>Saleh, Luqman</creator><creator>Dahlia, Dahlia</creator><creator>Mulyani, Rahmi</creator><creator>Itabashi, Yutaka</creator><general>John Wiley & Sons Australia, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TN</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0002-6216-7784</orcidid></search><sort><creationdate>202407</creationdate><title>Laboratory‐scale preparation of prostaglandins using acetone powder of the red alga Gracilaria vermiculophylla</title><author>Illijas, Muhammad Ikbal ; Suzuki, Nobuya ; Honda, Masaki ; Arma, Nur Rahmawaty ; Nasir, Andriani ; Saleh, Luqman ; Dahlia, Dahlia ; Mulyani, Rahmi ; Itabashi, Yutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2578-4d312c884aee59a87d97f2319d99752e6d8c029de8b3cddd2e39307526581a943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>15‐hydroperoxy‐PGE2</topic><topic>15‐keto‐PGE2</topic><topic>Acetone</topic><topic>Algae</topic><topic>Arachidonic acid</topic><topic>crude enzyme</topic><topic>Enzymes</topic><topic>Fatty acids</topic><topic>Gracilaria vermiculophylla</topic><topic>High-performance liquid chromatography</topic><topic>HPLC</topic><topic>In vitro methods and tests</topic><topic>Incubation</topic><topic>Liquid chromatography</topic><topic>LS‐MS</topic><topic>PGA2</topic><topic>PGE2</topic><topic>PGF2α</topic><topic>Polyunsaturated fatty acids</topic><topic>Powder</topic><topic>Prostaglandin E2</topic><topic>Prostaglandins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Illijas, Muhammad Ikbal</creatorcontrib><creatorcontrib>Suzuki, Nobuya</creatorcontrib><creatorcontrib>Honda, Masaki</creatorcontrib><creatorcontrib>Arma, Nur Rahmawaty</creatorcontrib><creatorcontrib>Nasir, Andriani</creatorcontrib><creatorcontrib>Saleh, Luqman</creatorcontrib><creatorcontrib>Dahlia, Dahlia</creatorcontrib><creatorcontrib>Mulyani, Rahmi</creatorcontrib><creatorcontrib>Itabashi, Yutaka</creatorcontrib><collection>CrossRef</collection><collection>Oceanic Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Phycological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Illijas, Muhammad Ikbal</au><au>Suzuki, Nobuya</au><au>Honda, Masaki</au><au>Arma, Nur Rahmawaty</au><au>Nasir, Andriani</au><au>Saleh, Luqman</au><au>Dahlia, Dahlia</au><au>Mulyani, Rahmi</au><au>Itabashi, Yutaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Laboratory‐scale preparation of prostaglandins using acetone powder of the red alga Gracilaria vermiculophylla</atitle><jtitle>Phycological research</jtitle><date>2024-07</date><risdate>2024</risdate><volume>72</volume><issue>3</issue><spage>159</spage><epage>166</epage><pages>159-166</pages><issn>1322-0829</issn><eissn>1440-1835</eissn><abstract>Summary
The red alga Gracilaria vermiculophylla is a prostaglandin (PG)‐producing macroalga. The alga is rich in polyunsaturated fatty acids with 20 carbon atoms, mainly arachidonic acid (AA), which is a precursor of PGs. The purpose of the present study was to analyze the ability of the red alga to produce PGs using acetone powder as the crude enzyme prepared from the alga. The acetone powder (250 mg) was incubated with different amounts of exogenous AA (0.1–4 mg). For the determination of PG contents, 5 μL of a sample solution (5 mL in water) consisting of acetone powder and AA was injected into the HPLC column. For PG analysis, an HPLC system connected with a mass spectrometer was used. Results of the study showed that the released PGs from incubation of acetone powder and AA consisted of PGE2, 15‐keto‐PGE2, 15‐hydroperoxy‐PGE2, PGA2, and PGF2α. The capability of the crude enzyme prepared from the red alga to produce PGs was affected by available oxygen and AA concentrations. The crude enzyme (250 mg) was capable of producing 164 and 141 μg of PGE2 and 15‐keto‐PGE2, respectively, from incubation with 250 μg of AA. This in vitro method could be a simple way to provide PGs in the laboratory.</abstract><cop>Kyoto, Japan</cop><pub>John Wiley & Sons Australia, Ltd</pub><doi>10.1111/pre.12548</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6216-7784</orcidid></addata></record> |
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subjects | 15‐hydroperoxy‐PGE2 15‐keto‐PGE2 Acetone Algae Arachidonic acid crude enzyme Enzymes Fatty acids Gracilaria vermiculophylla High-performance liquid chromatography HPLC In vitro methods and tests Incubation Liquid chromatography LS‐MS PGA2 PGE2 PGF2α Polyunsaturated fatty acids Powder Prostaglandin E2 Prostaglandins |
title | Laboratory‐scale preparation of prostaglandins using acetone powder of the red alga Gracilaria vermiculophylla |
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