Isolation and culture of protoplasts from the medicinal plants Centella asiatica
In the present investigation, protoplasts were isolated from cell suspensions initiated from leaf laminae and petioles using an enzyme mixture consisting of 1.5% (w/v) Cellulase R10, 1.0% (w/v) Macerozyme R10 and 0.5% (w/v) Driselase in CPW salts solution with 13% (w/v) mannitol as osmotic stabilize...
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| Format: | Article |
| Language: | English English |
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Sociedade Brasileira de Plantas Medicinais
2006
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| Online Access: | https://eprints.ums.edu.my/id/eprint/33395/1/Isolation%20and%20culture%20of%20protoplasts%20from%20the%20medicinal%20plants%20Centella%20asiatica.pdf https://eprints.ums.edu.my/id/eprint/33395/3/Isolation%20and%20culture%20of%20protoplasts%20from%20the%20medicinal%20plants%20Centella%20asiatica%20_ABSTRACT.pdf |
| _version_ | 1796911396178362368 |
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| author | Zaleha A. Aziz Davey, M. R. Lowe, K. C. Power, J. B. |
| author_facet | Zaleha A. Aziz Davey, M. R. Lowe, K. C. Power, J. B. |
| author_sort | Zaleha A. Aziz |
| collection | UMS |
| description | In the present investigation, protoplasts were isolated from cell suspensions initiated from leaf laminae and petioles using an enzyme mixture consisting of 1.5% (w/v) Cellulase R10, 1.0% (w/v) Macerozyme R10 and 0.5% (w/v) Driselase in CPW salts solution with 13% (w/v) mannitol as osmotic stabilizer. Yields and viabilities of isolated protoplasts were 1.2 x 105 ± 0.1 g-1 fresh weight and 20.8 ± 4.4% for protoplasts from lamina-derived cell suspensions and 7.9 x 105 ± 1.5 g-1 fresh weight and 79.3 ± 13.4% for protoplasts from petiole-derived cell suspensions. Protoplasts from lamina explant-derived cell suspensions were cultured at plating densities of 0.25 x 105 – 2.0 x 105 protoplasts ml-1 in half-strength B5 based medium containing 0.1 mgl-1 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.3 mgl1 zeatin, dispensed as semi-solid agarose droplets (each approx. 70 µl in volume) in 5.5 cm diameter Petri dishes (10 droplets per dish). First mitotic divisions of protoplast-derived cells were observed after 4 d of culture at an optimum plating density of 0.5 x 105 protoplasts ml-1, giving an initial plating efficiency at this time of 12.7 ± 0.6%. After 42 d of culture, protoplast-derived cell colonies were creamy-white in colour and each approx. 1 mm in diameter, with a final plating efficiency of 0.6 ± 0.2%. Cell colonies transferred to semi-solid proliferation medium containing 2,4-D (4.0 mgl-1) and zeatin (0.2 mgl-1) were creamy-yellow in appearance, whereas colonies cultured on medium devoid of these growth regulators became light green and compact. In the case of protoplasts from petiole-derived cell suspensions, culture in Murashige and Skoog (1962)-based medium supplemented with 2.0 mgl-1 alpha-naphthaleneacetic acid and 0.5 mgl-1 6-benzylaminopurine resulted in an initial plating efficiency of 19.3 ± 4.2% at an optimum plating density of 1.0 x 105 protoplasts ml-1. However, mitotic division was not sustained after this stage. Plant regeneration studies are on-going from protoplasts isolated from lamina-derived cell suspensions. |
| first_indexed | 2024-03-06T03:18:11Z |
| format | Article |
| id | ums.eprints-33395 |
| institution | Universiti Malaysia Sabah |
| language | English English |
| last_indexed | 2024-03-06T03:18:11Z |
| publishDate | 2006 |
| publisher | Sociedade Brasileira de Plantas Medicinais |
| record_format | dspace |
| spelling | ums.eprints-333952022-07-20T12:31:54Z https://eprints.ums.edu.my/id/eprint/33395/ Isolation and culture of protoplasts from the medicinal plants Centella asiatica Zaleha A. Aziz Davey, M. R. Lowe, K. C. Power, J. B. RS153-441 Materia medica SB1-1110 Plant culture In the present investigation, protoplasts were isolated from cell suspensions initiated from leaf laminae and petioles using an enzyme mixture consisting of 1.5% (w/v) Cellulase R10, 1.0% (w/v) Macerozyme R10 and 0.5% (w/v) Driselase in CPW salts solution with 13% (w/v) mannitol as osmotic stabilizer. Yields and viabilities of isolated protoplasts were 1.2 x 105 ± 0.1 g-1 fresh weight and 20.8 ± 4.4% for protoplasts from lamina-derived cell suspensions and 7.9 x 105 ± 1.5 g-1 fresh weight and 79.3 ± 13.4% for protoplasts from petiole-derived cell suspensions. Protoplasts from lamina explant-derived cell suspensions were cultured at plating densities of 0.25 x 105 – 2.0 x 105 protoplasts ml-1 in half-strength B5 based medium containing 0.1 mgl-1 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.3 mgl1 zeatin, dispensed as semi-solid agarose droplets (each approx. 70 µl in volume) in 5.5 cm diameter Petri dishes (10 droplets per dish). First mitotic divisions of protoplast-derived cells were observed after 4 d of culture at an optimum plating density of 0.5 x 105 protoplasts ml-1, giving an initial plating efficiency at this time of 12.7 ± 0.6%. After 42 d of culture, protoplast-derived cell colonies were creamy-white in colour and each approx. 1 mm in diameter, with a final plating efficiency of 0.6 ± 0.2%. Cell colonies transferred to semi-solid proliferation medium containing 2,4-D (4.0 mgl-1) and zeatin (0.2 mgl-1) were creamy-yellow in appearance, whereas colonies cultured on medium devoid of these growth regulators became light green and compact. In the case of protoplasts from petiole-derived cell suspensions, culture in Murashige and Skoog (1962)-based medium supplemented with 2.0 mgl-1 alpha-naphthaleneacetic acid and 0.5 mgl-1 6-benzylaminopurine resulted in an initial plating efficiency of 19.3 ± 4.2% at an optimum plating density of 1.0 x 105 protoplasts ml-1. However, mitotic division was not sustained after this stage. Plant regeneration studies are on-going from protoplasts isolated from lamina-derived cell suspensions. Sociedade Brasileira de Plantas Medicinais 2006 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/33395/1/Isolation%20and%20culture%20of%20protoplasts%20from%20the%20medicinal%20plants%20Centella%20asiatica.pdf text en https://eprints.ums.edu.my/id/eprint/33395/3/Isolation%20and%20culture%20of%20protoplasts%20from%20the%20medicinal%20plants%20Centella%20asiatica%20_ABSTRACT.pdf Zaleha A. Aziz and Davey, M. R. and Lowe, K. C. and Power, J. B. (2006) Isolation and culture of protoplasts from the medicinal plants Centella asiatica. Revista Brasileira de Plantas Medicinais, 8. pp. 105-109. ISSN 1516-0572 (P-ISSN) , 1983-084X (E-ISSN) https://www1.ibb.unesp.br/Home/Departamentos/Botanica/RBPM-RevistaBrasileiradePlantasMedicinais/8esp_105_109.pdf |
| spellingShingle | RS153-441 Materia medica SB1-1110 Plant culture Zaleha A. Aziz Davey, M. R. Lowe, K. C. Power, J. B. Isolation and culture of protoplasts from the medicinal plants Centella asiatica |
| title | Isolation and culture of protoplasts from the medicinal plants Centella asiatica |
| title_full | Isolation and culture of protoplasts from the medicinal plants Centella asiatica |
| title_fullStr | Isolation and culture of protoplasts from the medicinal plants Centella asiatica |
| title_full_unstemmed | Isolation and culture of protoplasts from the medicinal plants Centella asiatica |
| title_short | Isolation and culture of protoplasts from the medicinal plants Centella asiatica |
| title_sort | isolation and culture of protoplasts from the medicinal plants centella asiatica |
| topic | RS153-441 Materia medica SB1-1110 Plant culture |
| url | https://eprints.ums.edu.my/id/eprint/33395/1/Isolation%20and%20culture%20of%20protoplasts%20from%20the%20medicinal%20plants%20Centella%20asiatica.pdf https://eprints.ums.edu.my/id/eprint/33395/3/Isolation%20and%20culture%20of%20protoplasts%20from%20the%20medicinal%20plants%20Centella%20asiatica%20_ABSTRACT.pdf |
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