CO2-enriched air in a temporary immersion system induces photomixotrophism during in vitro multiplication in vanilla
The term in vitro photomixotrophism refers to the ability of explants to obtain metabolic energy from the culture medium and as a product of photosynthesis. The objective of this research was to study the physiological and biochemical mechanisms of V. planifolia during in vitro multiplication using...
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description | The term in vitro photomixotrophism refers to the ability of explants to obtain metabolic energy from the culture medium and as a product of photosynthesis. The objective of this research was to study the physiological and biochemical mechanisms of
V. planifolia
during in vitro multiplication using a photomixotrophic system with different sucrose contents (0, 15 and 30 g L
–1
) and CO
2
supply levels (500, 800 and 1200 ppm) using a Temporary Immersion Modular System (SMIT
®
). After 45 days of multiplication, response percentage, number of shoots per explant, shoot length, number of leaves per shoot, stomatal index (%), percentage of closed stomata, and chlorophyll, β-carotene, Phosphoenolpyruvate (PEP) and Rubisco contents were evaluated. In addition, the survival rate during acclimatization at 60 days was evaluated. For the multiplication stage, the highest response percentage was obtained in the treatments with 15 g L
–1
sucrose with 500 and 800 ppm CO
2
, and 30 g L
–1
sucrose with 500 ppm CO
2
. In the latter treatment, the best development parameters were obtained, with 14.75 shoots per explant, a shoot length of 2.38 cm and 2.5 leaves per shoot. In general, the highest chlorophyll, β-carotene, PEP and Rubisco contents were observed with 30 g L
–1
sucrose + CO
2
. No effects of the treatments on stomatal index (%) were observed, while the percentage of closed stomata showed differences among treatments. At the acclimatization stage, the highest survival percentages were obtained from the treatments of 30 g L
–1
sucrose with 500 and 800 ppm CO
2
. In conclusion, this study demonstrates physiological and biochemical mechanisms for a better understanding of photomixotrophism during in vitro multiplication in vanilla and may be applied to other species.
Key message
In vitro photomixotrophism can be induced by injecting carbon dioxide to promote photosynthesis. |
doi_str_mv | 10.1007/s11240-023-02546-y |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2871981039</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2871981039</sourcerecordid><originalsourceid>FETCH-LOGICAL-c319t-a9f98ba6b008d408f9a2f2e31338a2bbe30d7a63c4bb385996d7d9f368e49faf3</originalsourceid><addsrcrecordid>eNp9UE1LxDAUDKLguvoHPAU8R_PVNjnK4hcs7EXPIW0TN0vb1CQV--9NXcGbh8eDeTPzmAHgmuBbgnF1FwmhHCNMWZ6Cl2g-AStSVAwVmPNTsMKkrFApiuocXMR4wBiXjJMVSJsdRWYIrtmbFmoXoBughsn0ow86zND1vQnR-QHGOWY439upMRGOe5987758Cn7cu9jDdgpueF8MPl0GYT91yY2da3Ra9AuuB9d1-hKcWd1Fc_W71-Dt8eF184y2u6eXzf0WNYzIhLS0UtS6rDEWLcfCSk0tNYwwJjSta8NwW-mSNbyumSikLNuqlZaVwnBptWVrcHP0HYP_mExM6uCnMOSXioqKSEEwk5lFj6wm-BiDsWoMrs_ZFcFqaVcd21W5XfXTrpqziB1FcVxCm_Bn_Y_qG8w9gIc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2871981039</pqid></control><display><type>article</type><title>CO2-enriched air in a temporary immersion system induces photomixotrophism during in vitro multiplication in vanilla</title><source>SpringerLink Journals - AutoHoldings</source><creator>Luis, Spinoso‑Castillo José ; Jabín, Bello‑Bello Jericó</creator><creatorcontrib>Luis, Spinoso‑Castillo José ; Jabín, Bello‑Bello Jericó</creatorcontrib><description>The term in vitro photomixotrophism refers to the ability of explants to obtain metabolic energy from the culture medium and as a product of photosynthesis. The objective of this research was to study the physiological and biochemical mechanisms of
V. planifolia
during in vitro multiplication using a photomixotrophic system with different sucrose contents (0, 15 and 30 g L
–1
) and CO
2
supply levels (500, 800 and 1200 ppm) using a Temporary Immersion Modular System (SMIT
®
). After 45 days of multiplication, response percentage, number of shoots per explant, shoot length, number of leaves per shoot, stomatal index (%), percentage of closed stomata, and chlorophyll, β-carotene, Phosphoenolpyruvate (PEP) and Rubisco contents were evaluated. In addition, the survival rate during acclimatization at 60 days was evaluated. For the multiplication stage, the highest response percentage was obtained in the treatments with 15 g L
–1
sucrose with 500 and 800 ppm CO
2
, and 30 g L
–1
sucrose with 500 ppm CO
2
. In the latter treatment, the best development parameters were obtained, with 14.75 shoots per explant, a shoot length of 2.38 cm and 2.5 leaves per shoot. In general, the highest chlorophyll, β-carotene, PEP and Rubisco contents were observed with 30 g L
–1
sucrose + CO
2
. No effects of the treatments on stomatal index (%) were observed, while the percentage of closed stomata showed differences among treatments. At the acclimatization stage, the highest survival percentages were obtained from the treatments of 30 g L
–1
sucrose with 500 and 800 ppm CO
2
. In conclusion, this study demonstrates physiological and biochemical mechanisms for a better understanding of photomixotrophism during in vitro multiplication in vanilla and may be applied to other species.
Key message
In vitro photomixotrophism can be induced by injecting carbon dioxide to promote photosynthesis.</description><identifier>ISSN: 0167-6857</identifier><identifier>EISSN: 1573-5044</identifier><identifier>DOI: 10.1007/s11240-023-02546-y</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Acclimatization ; Biomedical and Life Sciences ; Carbon dioxide ; Carotene ; Chlorophyll ; Energy metabolism ; Explants ; Immersion ; Leaves ; Life Sciences ; Modular systems ; Multiplication ; Original Article ; Photosynthesis ; Physiology ; Plant Genetics and Genomics ; Plant Pathology ; Plant Physiology ; Plant Sciences ; Ribulose-bisphosphate carboxylase ; Shoots ; Stomata ; Submerging ; Sucrose ; Survival ; β-Carotene</subject><ispartof>Plant cell, tissue and organ culture, 2023-10, Vol.155 (1), p.29-39</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-a9f98ba6b008d408f9a2f2e31338a2bbe30d7a63c4bb385996d7d9f368e49faf3</citedby><cites>FETCH-LOGICAL-c319t-a9f98ba6b008d408f9a2f2e31338a2bbe30d7a63c4bb385996d7d9f368e49faf3</cites><orcidid>0000-0002-2617-3079</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11240-023-02546-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11240-023-02546-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Luis, Spinoso‑Castillo José</creatorcontrib><creatorcontrib>Jabín, Bello‑Bello Jericó</creatorcontrib><title>CO2-enriched air in a temporary immersion system induces photomixotrophism during in vitro multiplication in vanilla</title><title>Plant cell, tissue and organ culture</title><addtitle>Plant Cell Tiss Organ Cult</addtitle><description>The term in vitro photomixotrophism refers to the ability of explants to obtain metabolic energy from the culture medium and as a product of photosynthesis. The objective of this research was to study the physiological and biochemical mechanisms of
V. planifolia
during in vitro multiplication using a photomixotrophic system with different sucrose contents (0, 15 and 30 g L
–1
) and CO
2
supply levels (500, 800 and 1200 ppm) using a Temporary Immersion Modular System (SMIT
®
). After 45 days of multiplication, response percentage, number of shoots per explant, shoot length, number of leaves per shoot, stomatal index (%), percentage of closed stomata, and chlorophyll, β-carotene, Phosphoenolpyruvate (PEP) and Rubisco contents were evaluated. In addition, the survival rate during acclimatization at 60 days was evaluated. For the multiplication stage, the highest response percentage was obtained in the treatments with 15 g L
–1
sucrose with 500 and 800 ppm CO
2
, and 30 g L
–1
sucrose with 500 ppm CO
2
. In the latter treatment, the best development parameters were obtained, with 14.75 shoots per explant, a shoot length of 2.38 cm and 2.5 leaves per shoot. In general, the highest chlorophyll, β-carotene, PEP and Rubisco contents were observed with 30 g L
–1
sucrose + CO
2
. No effects of the treatments on stomatal index (%) were observed, while the percentage of closed stomata showed differences among treatments. At the acclimatization stage, the highest survival percentages were obtained from the treatments of 30 g L
–1
sucrose with 500 and 800 ppm CO
2
. In conclusion, this study demonstrates physiological and biochemical mechanisms for a better understanding of photomixotrophism during in vitro multiplication in vanilla and may be applied to other species.
Key message
In vitro photomixotrophism can be induced by injecting carbon dioxide to promote photosynthesis.</description><subject>Acclimatization</subject><subject>Biomedical and Life Sciences</subject><subject>Carbon dioxide</subject><subject>Carotene</subject><subject>Chlorophyll</subject><subject>Energy metabolism</subject><subject>Explants</subject><subject>Immersion</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Modular systems</subject><subject>Multiplication</subject><subject>Original Article</subject><subject>Photosynthesis</subject><subject>Physiology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Pathology</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Ribulose-bisphosphate carboxylase</subject><subject>Shoots</subject><subject>Stomata</subject><subject>Submerging</subject><subject>Sucrose</subject><subject>Survival</subject><subject>β-Carotene</subject><issn>0167-6857</issn><issn>1573-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UE1LxDAUDKLguvoHPAU8R_PVNjnK4hcs7EXPIW0TN0vb1CQV--9NXcGbh8eDeTPzmAHgmuBbgnF1FwmhHCNMWZ6Cl2g-AStSVAwVmPNTsMKkrFApiuocXMR4wBiXjJMVSJsdRWYIrtmbFmoXoBughsn0ow86zND1vQnR-QHGOWY439upMRGOe5987758Cn7cu9jDdgpueF8MPl0GYT91yY2da3Ra9AuuB9d1-hKcWd1Fc_W71-Dt8eF184y2u6eXzf0WNYzIhLS0UtS6rDEWLcfCSk0tNYwwJjSta8NwW-mSNbyumSikLNuqlZaVwnBptWVrcHP0HYP_mExM6uCnMOSXioqKSEEwk5lFj6wm-BiDsWoMrs_ZFcFqaVcd21W5XfXTrpqziB1FcVxCm_Bn_Y_qG8w9gIc</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Luis, Spinoso‑Castillo José</creator><creator>Jabín, Bello‑Bello Jericó</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M0K</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><orcidid>https://orcid.org/0000-0002-2617-3079</orcidid></search><sort><creationdate>20231001</creationdate><title>CO2-enriched air in a temporary immersion system induces photomixotrophism during in vitro multiplication in vanilla</title><author>Luis, Spinoso‑Castillo José ; Jabín, Bello‑Bello Jericó</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-a9f98ba6b008d408f9a2f2e31338a2bbe30d7a63c4bb385996d7d9f368e49faf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acclimatization</topic><topic>Biomedical and Life Sciences</topic><topic>Carbon dioxide</topic><topic>Carotene</topic><topic>Chlorophyll</topic><topic>Energy metabolism</topic><topic>Explants</topic><topic>Immersion</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Modular systems</topic><topic>Multiplication</topic><topic>Original Article</topic><topic>Photosynthesis</topic><topic>Physiology</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Pathology</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Ribulose-bisphosphate carboxylase</topic><topic>Shoots</topic><topic>Stomata</topic><topic>Submerging</topic><topic>Sucrose</topic><topic>Survival</topic><topic>β-Carotene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luis, Spinoso‑Castillo José</creatorcontrib><creatorcontrib>Jabín, Bello‑Bello Jericó</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</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 Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Plant cell, tissue and organ culture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luis, Spinoso‑Castillo José</au><au>Jabín, Bello‑Bello Jericó</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CO2-enriched air in a temporary immersion system induces photomixotrophism during in vitro multiplication in vanilla</atitle><jtitle>Plant cell, tissue and organ culture</jtitle><stitle>Plant Cell Tiss Organ Cult</stitle><date>2023-10-01</date><risdate>2023</risdate><volume>155</volume><issue>1</issue><spage>29</spage><epage>39</epage><pages>29-39</pages><issn>0167-6857</issn><eissn>1573-5044</eissn><abstract>The term in vitro photomixotrophism refers to the ability of explants to obtain metabolic energy from the culture medium and as a product of photosynthesis. The objective of this research was to study the physiological and biochemical mechanisms of
V. planifolia
during in vitro multiplication using a photomixotrophic system with different sucrose contents (0, 15 and 30 g L
–1
) and CO
2
supply levels (500, 800 and 1200 ppm) using a Temporary Immersion Modular System (SMIT
®
). After 45 days of multiplication, response percentage, number of shoots per explant, shoot length, number of leaves per shoot, stomatal index (%), percentage of closed stomata, and chlorophyll, β-carotene, Phosphoenolpyruvate (PEP) and Rubisco contents were evaluated. In addition, the survival rate during acclimatization at 60 days was evaluated. For the multiplication stage, the highest response percentage was obtained in the treatments with 15 g L
–1
sucrose with 500 and 800 ppm CO
2
, and 30 g L
–1
sucrose with 500 ppm CO
2
. In the latter treatment, the best development parameters were obtained, with 14.75 shoots per explant, a shoot length of 2.38 cm and 2.5 leaves per shoot. In general, the highest chlorophyll, β-carotene, PEP and Rubisco contents were observed with 30 g L
–1
sucrose + CO
2
. No effects of the treatments on stomatal index (%) were observed, while the percentage of closed stomata showed differences among treatments. At the acclimatization stage, the highest survival percentages were obtained from the treatments of 30 g L
–1
sucrose with 500 and 800 ppm CO
2
. In conclusion, this study demonstrates physiological and biochemical mechanisms for a better understanding of photomixotrophism during in vitro multiplication in vanilla and may be applied to other species.
Key message
In vitro photomixotrophism can be induced by injecting carbon dioxide to promote photosynthesis.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11240-023-02546-y</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2617-3079</orcidid></addata></record> |
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source | SpringerLink Journals - AutoHoldings |
subjects | Acclimatization Biomedical and Life Sciences Carbon dioxide Carotene Chlorophyll Energy metabolism Explants Immersion Leaves Life Sciences Modular systems Multiplication Original Article Photosynthesis Physiology Plant Genetics and Genomics Plant Pathology Plant Physiology Plant Sciences Ribulose-bisphosphate carboxylase Shoots Stomata Submerging Sucrose Survival β-Carotene |
title | CO2-enriched air in a temporary immersion system induces photomixotrophism during in vitro multiplication in vanilla |
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