Hairy root culture of Strobilanthes cusia for the production and enhancement of indigo biosynthesis
Strobilanthes cusia is an indigo-yielding plant and scarcity of both wild and cultivated plants has increased the supply pressure of the natural dye. Since hairy root cultures are suitable for the in vitro production of secondary metabolites, the hairy root culture of Strobilanthes cusia was establi...
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description | Strobilanthes cusia
is an indigo-yielding plant and scarcity of both wild and cultivated plants has increased the supply pressure of the natural dye. Since hairy root cultures are suitable for the in vitro production of secondary metabolites, the hairy root culture of
Strobilanthes cusia
was established using two
Rhizobium rhizogenes
strains (ATCC 15834 and MTCC 532). Polymerase chain reaction (PCR) using
rol B
primer confirmed the molecular evidence of hairy root transformation. The differential transformation frequency was studied based on factors like explants types (leaves, shoot tips, and stem); infection techniques, infection period, co-cultivation period, bacterial strain types, acetosyringone concentration, and antibiotic treatment conditions. Leaf explants, infected with ATCC 15834 exhibited the highest induction rate (58.67%) among the three explants. The most efficient hairy root transformation was achieved with the immersion technique, involving 10 min of infection and 5 days of co-cultivation using 100 µM acetosyringone during infection. When the indigo content of the hairy roots and different parts of in vitro plantlets were compared, the hairy roots produced 0.314 mg/g fresh weight (FW) of indigo, slightly more than the roots (0.21 mg/g FW), but less than the leaves (1.08 mg/g FW) of in vitro plantlets. Further, the indigo content of the hairy root cultures treated with 200 µM indican and 200 µM salicylic acid were enhanced up to 0.78 mg/g FW and 0.71 mg/g FW, respectively. Thus, this study reveals the potential of hairy roots of
S. cusia
for indigo biosynthesis, which may serve as a potential alternative source for natural indigo.
Key message
First report of hairy root induction of
Strobilanthes cusia
and elicitation of the indigo content by using different elicitors and precursors feeding. |
doi_str_mv | 10.1007/s11240-024-02791-9 |
format | Article |
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is an indigo-yielding plant and scarcity of both wild and cultivated plants has increased the supply pressure of the natural dye. Since hairy root cultures are suitable for the in vitro production of secondary metabolites, the hairy root culture of
Strobilanthes cusia
was established using two
Rhizobium rhizogenes
strains (ATCC 15834 and MTCC 532). Polymerase chain reaction (PCR) using
rol B
primer confirmed the molecular evidence of hairy root transformation. The differential transformation frequency was studied based on factors like explants types (leaves, shoot tips, and stem); infection techniques, infection period, co-cultivation period, bacterial strain types, acetosyringone concentration, and antibiotic treatment conditions. Leaf explants, infected with ATCC 15834 exhibited the highest induction rate (58.67%) among the three explants. The most efficient hairy root transformation was achieved with the immersion technique, involving 10 min of infection and 5 days of co-cultivation using 100 µM acetosyringone during infection. When the indigo content of the hairy roots and different parts of in vitro plantlets were compared, the hairy roots produced 0.314 mg/g fresh weight (FW) of indigo, slightly more than the roots (0.21 mg/g FW), but less than the leaves (1.08 mg/g FW) of in vitro plantlets. Further, the indigo content of the hairy root cultures treated with 200 µM indican and 200 µM salicylic acid were enhanced up to 0.78 mg/g FW and 0.71 mg/g FW, respectively. Thus, this study reveals the potential of hairy roots of
S. cusia
for indigo biosynthesis, which may serve as a potential alternative source for natural indigo.
Key message
First report of hairy root induction of
Strobilanthes cusia
and elicitation of the indigo content by using different elicitors and precursors feeding.</description><identifier>ISSN: 0167-6857</identifier><identifier>EISSN: 1573-5044</identifier><identifier>DOI: 10.1007/s11240-024-02791-9</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Acetosyringone ; Biomedical and Life Sciences ; Biosynthesis ; Cultivated plants ; Cultivation ; Explants ; Genetic transformation ; Hairy root ; Indigo ; Infections ; Leaves ; Life Sciences ; Metabolites ; Original Article ; Plant Genetics and Genomics ; Plant Pathology ; Plant Physiology ; Plant Sciences ; Plantlets ; Polymerase chain reaction ; Roots ; Salicylic acid ; Secondary metabolites</subject><ispartof>Plant cell, tissue and organ culture, 2024-06, Vol.157 (3), p.62, Article 62</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2024. 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><cites>FETCH-LOGICAL-c200t-3a0337554150e16293286015919b2dc8962e8be64a77f886a1462dc1ffc62e513</cites><orcidid>0000-0001-7312-8695</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/s11240-024-02791-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11240-024-02791-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Devi, Rajkumari Lunphasana</creatorcontrib><creatorcontrib>Devi, Sanasam Thoibi</creatorcontrib><creatorcontrib>Sanatombi, Keithellakpam</creatorcontrib><title>Hairy root culture of Strobilanthes cusia for the production and enhancement of indigo biosynthesis</title><title>Plant cell, tissue and organ culture</title><addtitle>Plant Cell Tiss Organ Cult</addtitle><description>Strobilanthes cusia
is an indigo-yielding plant and scarcity of both wild and cultivated plants has increased the supply pressure of the natural dye. Since hairy root cultures are suitable for the in vitro production of secondary metabolites, the hairy root culture of
Strobilanthes cusia
was established using two
Rhizobium rhizogenes
strains (ATCC 15834 and MTCC 532). Polymerase chain reaction (PCR) using
rol B
primer confirmed the molecular evidence of hairy root transformation. The differential transformation frequency was studied based on factors like explants types (leaves, shoot tips, and stem); infection techniques, infection period, co-cultivation period, bacterial strain types, acetosyringone concentration, and antibiotic treatment conditions. Leaf explants, infected with ATCC 15834 exhibited the highest induction rate (58.67%) among the three explants. The most efficient hairy root transformation was achieved with the immersion technique, involving 10 min of infection and 5 days of co-cultivation using 100 µM acetosyringone during infection. When the indigo content of the hairy roots and different parts of in vitro plantlets were compared, the hairy roots produced 0.314 mg/g fresh weight (FW) of indigo, slightly more than the roots (0.21 mg/g FW), but less than the leaves (1.08 mg/g FW) of in vitro plantlets. Further, the indigo content of the hairy root cultures treated with 200 µM indican and 200 µM salicylic acid were enhanced up to 0.78 mg/g FW and 0.71 mg/g FW, respectively. Thus, this study reveals the potential of hairy roots of
S. cusia
for indigo biosynthesis, which may serve as a potential alternative source for natural indigo.
Key message
First report of hairy root induction of
Strobilanthes cusia
and elicitation of the indigo content by using different elicitors and precursors feeding.</description><subject>Acetosyringone</subject><subject>Biomedical and Life Sciences</subject><subject>Biosynthesis</subject><subject>Cultivated plants</subject><subject>Cultivation</subject><subject>Explants</subject><subject>Genetic transformation</subject><subject>Hairy root</subject><subject>Indigo</subject><subject>Infections</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Metabolites</subject><subject>Original Article</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Pathology</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Plantlets</subject><subject>Polymerase chain reaction</subject><subject>Roots</subject><subject>Salicylic acid</subject><subject>Secondary metabolites</subject><issn>0167-6857</issn><issn>1573-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE9PAyEQxYnRxFr9Ap5IPK8Of3f3aBq1JiYe1DNhWbalaaECe-i3l3ZNvHmYkGHe7w08hG4J3BOA-iERQjlUQHmpuiVVe4ZmRNSsEsD5OZoBkXUlG1FfoquUNgAgGSczZJbaxQOOIWRsxm0eo8VhwB85hs5ttc9rm8ogOY2HEHFp8T6GfjTZBY-177H1a-2N3Vmfj6TzvVsF3LmQDifapWt0Mehtsje_5xx9PT99LpbV2_vL6-LxrTIUIFdMA2O1EJwIsETSltFGAhEtaTvam6aV1DadlVzX9dA0UhMuyz0ZBlMmgrA5upt8ywu_R5uy2oQx-rJSMZAg6fHTRUUnlYkhpWgHtY9up-NBEVDHMNUUpiphqlOYqi0Qm6BUxH5l45_1P9QPA4l3Qw</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Devi, Rajkumari Lunphasana</creator><creator>Devi, Sanasam Thoibi</creator><creator>Sanatombi, Keithellakpam</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-7312-8695</orcidid></search><sort><creationdate>20240601</creationdate><title>Hairy root culture of Strobilanthes cusia for the production and enhancement of indigo biosynthesis</title><author>Devi, Rajkumari Lunphasana ; Devi, Sanasam Thoibi ; Sanatombi, Keithellakpam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c200t-3a0337554150e16293286015919b2dc8962e8be64a77f886a1462dc1ffc62e513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acetosyringone</topic><topic>Biomedical and Life Sciences</topic><topic>Biosynthesis</topic><topic>Cultivated plants</topic><topic>Cultivation</topic><topic>Explants</topic><topic>Genetic transformation</topic><topic>Hairy root</topic><topic>Indigo</topic><topic>Infections</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Metabolites</topic><topic>Original Article</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Pathology</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Plantlets</topic><topic>Polymerase chain reaction</topic><topic>Roots</topic><topic>Salicylic acid</topic><topic>Secondary metabolites</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Devi, Rajkumari Lunphasana</creatorcontrib><creatorcontrib>Devi, Sanasam Thoibi</creatorcontrib><creatorcontrib>Sanatombi, Keithellakpam</creatorcontrib><collection>CrossRef</collection><jtitle>Plant cell, tissue and organ culture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Devi, Rajkumari Lunphasana</au><au>Devi, Sanasam Thoibi</au><au>Sanatombi, Keithellakpam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hairy root culture of Strobilanthes cusia for the production and enhancement of indigo biosynthesis</atitle><jtitle>Plant cell, tissue and organ culture</jtitle><stitle>Plant Cell Tiss Organ Cult</stitle><date>2024-06-01</date><risdate>2024</risdate><volume>157</volume><issue>3</issue><spage>62</spage><pages>62-</pages><artnum>62</artnum><issn>0167-6857</issn><eissn>1573-5044</eissn><abstract>Strobilanthes cusia
is an indigo-yielding plant and scarcity of both wild and cultivated plants has increased the supply pressure of the natural dye. Since hairy root cultures are suitable for the in vitro production of secondary metabolites, the hairy root culture of
Strobilanthes cusia
was established using two
Rhizobium rhizogenes
strains (ATCC 15834 and MTCC 532). Polymerase chain reaction (PCR) using
rol B
primer confirmed the molecular evidence of hairy root transformation. The differential transformation frequency was studied based on factors like explants types (leaves, shoot tips, and stem); infection techniques, infection period, co-cultivation period, bacterial strain types, acetosyringone concentration, and antibiotic treatment conditions. Leaf explants, infected with ATCC 15834 exhibited the highest induction rate (58.67%) among the three explants. The most efficient hairy root transformation was achieved with the immersion technique, involving 10 min of infection and 5 days of co-cultivation using 100 µM acetosyringone during infection. When the indigo content of the hairy roots and different parts of in vitro plantlets were compared, the hairy roots produced 0.314 mg/g fresh weight (FW) of indigo, slightly more than the roots (0.21 mg/g FW), but less than the leaves (1.08 mg/g FW) of in vitro plantlets. Further, the indigo content of the hairy root cultures treated with 200 µM indican and 200 µM salicylic acid were enhanced up to 0.78 mg/g FW and 0.71 mg/g FW, respectively. Thus, this study reveals the potential of hairy roots of
S. cusia
for indigo biosynthesis, which may serve as a potential alternative source for natural indigo.
Key message
First report of hairy root induction of
Strobilanthes cusia
and elicitation of the indigo content by using different elicitors and precursors feeding.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s11240-024-02791-9</doi><orcidid>https://orcid.org/0000-0001-7312-8695</orcidid></addata></record> |
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subjects | Acetosyringone Biomedical and Life Sciences Biosynthesis Cultivated plants Cultivation Explants Genetic transformation Hairy root Indigo Infections Leaves Life Sciences Metabolites Original Article Plant Genetics and Genomics Plant Pathology Plant Physiology Plant Sciences Plantlets Polymerase chain reaction Roots Salicylic acid Secondary metabolites |
title | Hairy root culture of Strobilanthes cusia for the production and enhancement of indigo biosynthesis |
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