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Histological assessment of regenerating plants at callus, shoot organogenesis and plantlet stages during the in vitro micropropagation of Asparagus cochinchinensis
In this study, we developed a repeatable in vitro micropropagation protocol for the medicinal plant Asparagus cochinchinensis, based on indirect organogenesis using leaf segments cut from seedlings of in vitro-germinated seeds. We obtained 85% callus induction from the leaf segments within 4–5 weeks...
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Published in: | Plant cell, tissue and organ culture tissue and organ culture, 2021-02, Vol.144 (2), p.421-433 |
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description | In this study, we developed a repeatable in vitro micropropagation protocol for the medicinal plant
Asparagus cochinchinensis,
based on indirect organogenesis using leaf segments cut from seedlings of in vitro-germinated seeds. We obtained 85% callus induction from the leaf segments within 4–5 weeks when grown on Murashige and Skoog (MS) medium supplemented with benzylaminopurine (BAP, 1.0 mg/L) and 1-naphthaleneacetic acid (NAA, 0.5 mg/L). We found that MS media supplemented with Kn (1.0 mg/L) in combination with NAA (1.0 mg/L) and BAP (1.0 mg/L) combined with NAA (0.5 mg/L) were the most effective in promoting shoot regeneration, yielding plantlets with 6.72 and 6.48 shoots per culture, respectively. When cultured on PGR-free half-strength MS medium, regenerated plants developed root systems with an average 11.0 roots per shoot cluster and an average length of 36.14 mm at 9 weeks. During acclimatization, regenerated plantlets showed 96.4% survival and exhibited normal growth characteristics and morphology. We also made an attempt to directly regenerate
A. cochinchinensis
from shoot apices but it was futile. Histological analyses revealed the presence of crystal idioblasts in young leaves from the early stages of leaf differentiation. The leaf-based plant regeneration technique developed herein could be employed for large-scale propagation of the plants over a short time period, thereby substantially contributing to the germplasm preservation and rapid propagation of
A. cochinchinensis
.
Key message
A repeatable in vitro micropropagation protocol for Asparagus cochinchinensis was developed based on indirect organogenesis. Histological analysis revealed crystal idioblasts for the first time in leaf primordia of this species. |
doi_str_mv | 10.1007/s11240-020-01967-3 |
format | article |
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Asparagus cochinchinensis,
based on indirect organogenesis using leaf segments cut from seedlings of in vitro-germinated seeds. We obtained 85% callus induction from the leaf segments within 4–5 weeks when grown on Murashige and Skoog (MS) medium supplemented with benzylaminopurine (BAP, 1.0 mg/L) and 1-naphthaleneacetic acid (NAA, 0.5 mg/L). We found that MS media supplemented with Kn (1.0 mg/L) in combination with NAA (1.0 mg/L) and BAP (1.0 mg/L) combined with NAA (0.5 mg/L) were the most effective in promoting shoot regeneration, yielding plantlets with 6.72 and 6.48 shoots per culture, respectively. When cultured on PGR-free half-strength MS medium, regenerated plants developed root systems with an average 11.0 roots per shoot cluster and an average length of 36.14 mm at 9 weeks. During acclimatization, regenerated plantlets showed 96.4% survival and exhibited normal growth characteristics and morphology. We also made an attempt to directly regenerate
A. cochinchinensis
from shoot apices but it was futile. Histological analyses revealed the presence of crystal idioblasts in young leaves from the early stages of leaf differentiation. The leaf-based plant regeneration technique developed herein could be employed for large-scale propagation of the plants over a short time period, thereby substantially contributing to the germplasm preservation and rapid propagation of
A. cochinchinensis
.
Key message
A repeatable in vitro micropropagation protocol for Asparagus cochinchinensis was developed based on indirect organogenesis. Histological analysis revealed crystal idioblasts for the first time in leaf primordia of this species.</description><identifier>ISSN: 0167-6857</identifier><identifier>EISSN: 1573-5044</identifier><identifier>DOI: 10.1007/s11240-020-01967-3</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Acclimatization ; Asparagus ; Benzyladenine ; Biomedical and Life Sciences ; Callus ; Germplasm ; Herbal medicine ; Leaves ; Life Sciences ; Medicinal plants ; Micropropagation ; Morphology ; Naphthaleneacetic acid ; Organogenesis ; Original Article ; Physical characteristics ; Plant Genetics and Genomics ; Plant Pathology ; Plant Physiology ; Plant propagation ; Plant Sciences ; Plantlets ; Plants ; Primordia ; Propagation ; Regeneration ; Seedlings ; Seeds ; Segments ; Shoots ; Vegetables</subject><ispartof>Plant cell, tissue and organ culture, 2021-02, Vol.144 (2), p.421-433</ispartof><rights>Springer Nature B.V. 2020</rights><rights>Springer Nature B.V. 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-bee12d023bcfec284b29b4f6f5cacb8a7315d557b54bb6d528987062abf1e9a43</citedby><cites>FETCH-LOGICAL-c356t-bee12d023bcfec284b29b4f6f5cacb8a7315d557b54bb6d528987062abf1e9a43</cites><orcidid>0000-0002-0300-5953</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kim, Yong-Goo</creatorcontrib><creatorcontrib>Okello, Denis</creatorcontrib><creatorcontrib>Yang, Sungyu</creatorcontrib><creatorcontrib>Komakech, Richard</creatorcontrib><creatorcontrib>Rahmat, Endang</creatorcontrib><creatorcontrib>Kang, Youngmin</creatorcontrib><title>Histological assessment of regenerating plants at callus, shoot organogenesis and plantlet stages during the in vitro micropropagation of Asparagus cochinchinensis</title><title>Plant cell, tissue and organ culture</title><addtitle>Plant Cell Tiss Organ Cult</addtitle><description>In this study, we developed a repeatable in vitro micropropagation protocol for the medicinal plant
Asparagus cochinchinensis,
based on indirect organogenesis using leaf segments cut from seedlings of in vitro-germinated seeds. We obtained 85% callus induction from the leaf segments within 4–5 weeks when grown on Murashige and Skoog (MS) medium supplemented with benzylaminopurine (BAP, 1.0 mg/L) and 1-naphthaleneacetic acid (NAA, 0.5 mg/L). We found that MS media supplemented with Kn (1.0 mg/L) in combination with NAA (1.0 mg/L) and BAP (1.0 mg/L) combined with NAA (0.5 mg/L) were the most effective in promoting shoot regeneration, yielding plantlets with 6.72 and 6.48 shoots per culture, respectively. When cultured on PGR-free half-strength MS medium, regenerated plants developed root systems with an average 11.0 roots per shoot cluster and an average length of 36.14 mm at 9 weeks. During acclimatization, regenerated plantlets showed 96.4% survival and exhibited normal growth characteristics and morphology. We also made an attempt to directly regenerate
A. cochinchinensis
from shoot apices but it was futile. Histological analyses revealed the presence of crystal idioblasts in young leaves from the early stages of leaf differentiation. The leaf-based plant regeneration technique developed herein could be employed for large-scale propagation of the plants over a short time period, thereby substantially contributing to the germplasm preservation and rapid propagation of
A. cochinchinensis
.
Key message
A repeatable in vitro micropropagation protocol for Asparagus cochinchinensis was developed based on indirect organogenesis. Histological analysis revealed crystal idioblasts for the first time in leaf primordia of this species.</description><subject>Acclimatization</subject><subject>Asparagus</subject><subject>Benzyladenine</subject><subject>Biomedical and Life Sciences</subject><subject>Callus</subject><subject>Germplasm</subject><subject>Herbal medicine</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Medicinal plants</subject><subject>Micropropagation</subject><subject>Morphology</subject><subject>Naphthaleneacetic acid</subject><subject>Organogenesis</subject><subject>Original Article</subject><subject>Physical characteristics</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Pathology</subject><subject>Plant Physiology</subject><subject>Plant propagation</subject><subject>Plant Sciences</subject><subject>Plantlets</subject><subject>Plants</subject><subject>Primordia</subject><subject>Propagation</subject><subject>Regeneration</subject><subject>Seedlings</subject><subject>Seeds</subject><subject>Segments</subject><subject>Shoots</subject><subject>Vegetables</subject><issn>0167-6857</issn><issn>1573-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kc2KFTEQhYM44HWcF3AVcGuP-e2f5TCoMzDgRtchSVf3zdA3aVNpwefxRU3bgjshRaDynVNJDiFvObvljHUfkHOhWMNELT60XSNfkBPXnWw0U-olOTFem22vu1fkNeIzY6yVip_Ir4eAJS1pDt4u1CIC4gVioWmiGWaIkG0JcabrYmNBagut4LLhe4rnlCqXZxvTDmKox3E8yAUKxWJnQDpueTcoZ6Ah0h-h5EQvwee01mXnap_iPu4OV5vtvCH1yZ9D3AtidX1Dria7INz83a_Jt08fv94_NE9fPj_e3z01Xuq2NA6Ai5EJ6fwEXvTKicGpqZ20t971tpNcj1p3Tivn2lGLfug71grrJg6DVfKavDt868W-b4DFPKctxzrSCNUrxcUwiEqJg6ovQMwwmTWHi80_DWdmD8McYZgahvkThpFVJA8RrvtnQP5n_R_Vb91gkls</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Kim, Yong-Goo</creator><creator>Okello, Denis</creator><creator>Yang, Sungyu</creator><creator>Komakech, Richard</creator><creator>Rahmat, Endang</creator><creator>Kang, Youngmin</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/0000-0002-0300-5953</orcidid></search><sort><creationdate>20210201</creationdate><title>Histological assessment of regenerating plants at callus, shoot organogenesis and plantlet stages during the in vitro micropropagation of Asparagus cochinchinensis</title><author>Kim, Yong-Goo ; Okello, Denis ; Yang, Sungyu ; Komakech, Richard ; Rahmat, Endang ; Kang, Youngmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-bee12d023bcfec284b29b4f6f5cacb8a7315d557b54bb6d528987062abf1e9a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acclimatization</topic><topic>Asparagus</topic><topic>Benzyladenine</topic><topic>Biomedical and Life Sciences</topic><topic>Callus</topic><topic>Germplasm</topic><topic>Herbal medicine</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Medicinal plants</topic><topic>Micropropagation</topic><topic>Morphology</topic><topic>Naphthaleneacetic acid</topic><topic>Organogenesis</topic><topic>Original Article</topic><topic>Physical characteristics</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Pathology</topic><topic>Plant Physiology</topic><topic>Plant propagation</topic><topic>Plant Sciences</topic><topic>Plantlets</topic><topic>Plants</topic><topic>Primordia</topic><topic>Propagation</topic><topic>Regeneration</topic><topic>Seedlings</topic><topic>Seeds</topic><topic>Segments</topic><topic>Shoots</topic><topic>Vegetables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Yong-Goo</creatorcontrib><creatorcontrib>Okello, Denis</creatorcontrib><creatorcontrib>Yang, Sungyu</creatorcontrib><creatorcontrib>Komakech, Richard</creatorcontrib><creatorcontrib>Rahmat, Endang</creatorcontrib><creatorcontrib>Kang, Youngmin</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</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>Agriculture 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>Kim, Yong-Goo</au><au>Okello, Denis</au><au>Yang, Sungyu</au><au>Komakech, Richard</au><au>Rahmat, Endang</au><au>Kang, Youngmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histological assessment of regenerating plants at callus, shoot organogenesis and plantlet stages during the in vitro micropropagation of Asparagus cochinchinensis</atitle><jtitle>Plant cell, tissue and organ culture</jtitle><stitle>Plant Cell Tiss Organ Cult</stitle><date>2021-02-01</date><risdate>2021</risdate><volume>144</volume><issue>2</issue><spage>421</spage><epage>433</epage><pages>421-433</pages><issn>0167-6857</issn><eissn>1573-5044</eissn><abstract>In this study, we developed a repeatable in vitro micropropagation protocol for the medicinal plant
Asparagus cochinchinensis,
based on indirect organogenesis using leaf segments cut from seedlings of in vitro-germinated seeds. We obtained 85% callus induction from the leaf segments within 4–5 weeks when grown on Murashige and Skoog (MS) medium supplemented with benzylaminopurine (BAP, 1.0 mg/L) and 1-naphthaleneacetic acid (NAA, 0.5 mg/L). We found that MS media supplemented with Kn (1.0 mg/L) in combination with NAA (1.0 mg/L) and BAP (1.0 mg/L) combined with NAA (0.5 mg/L) were the most effective in promoting shoot regeneration, yielding plantlets with 6.72 and 6.48 shoots per culture, respectively. When cultured on PGR-free half-strength MS medium, regenerated plants developed root systems with an average 11.0 roots per shoot cluster and an average length of 36.14 mm at 9 weeks. During acclimatization, regenerated plantlets showed 96.4% survival and exhibited normal growth characteristics and morphology. We also made an attempt to directly regenerate
A. cochinchinensis
from shoot apices but it was futile. Histological analyses revealed the presence of crystal idioblasts in young leaves from the early stages of leaf differentiation. The leaf-based plant regeneration technique developed herein could be employed for large-scale propagation of the plants over a short time period, thereby substantially contributing to the germplasm preservation and rapid propagation of
A. cochinchinensis
.
Key message
A repeatable in vitro micropropagation protocol for Asparagus cochinchinensis was developed based on indirect organogenesis. Histological analysis revealed crystal idioblasts for the first time in leaf primordia of this species.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11240-020-01967-3</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-0300-5953</orcidid></addata></record> |
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language | eng |
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subjects | Acclimatization Asparagus Benzyladenine Biomedical and Life Sciences Callus Germplasm Herbal medicine Leaves Life Sciences Medicinal plants Micropropagation Morphology Naphthaleneacetic acid Organogenesis Original Article Physical characteristics Plant Genetics and Genomics Plant Pathology Plant Physiology Plant propagation Plant Sciences Plantlets Plants Primordia Propagation Regeneration Seedlings Seeds Segments Shoots Vegetables |
title | Histological assessment of regenerating plants at callus, shoot organogenesis and plantlet stages during the in vitro micropropagation of Asparagus cochinchinensis |
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