Isolation, culture of protoplasts of Angelica gigas Nakai and regeneration of plants via somatic embryogenesis (Record no. 55031)

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003 - CONTROL NUMBER IDENTIFIER
control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625162458.0
040 ## - CATALOGING SOURCE
Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-20952
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
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245 10 - TITLE STATEMENT
Title Isolation, culture of protoplasts of Angelica gigas Nakai and regeneration of plants via somatic embryogenesis
490 0# - SERIES STATEMENT
Volume/sequential designation Plant Cell, Tissue and Organ Culture, 156(2), p.40, 2024
520 3# - SUMMARY, ETC.
Summary, etc. In plant biotechnology, protoplasts are a versatile tool since they are very helpful for both fundamental biology studies and for genetic improvement and genome editing studies. In many plant species, however, reproducible regeneration from protoplasts continues to be a bottleneck. In the present study, we report the development of an efficient method for protoplast isolation, and plant regeneration in Angelica gigas via indirect somatic embryogenesis. Protoplasts were isolated from embryogenic callus using an enzyme mixture of 1.0 percent Viscozyme® L?+?1 percent Celluclast® 1.5 L?+?0.5 percent Pectinex® XXL with 7 h treatments. Initially, protoplasts were cultured in MS, modified MS (NH4NO3-free medium), and KM media, and viability and cell division data showed the MS medium was suitable for protoplast culture. Subsequently, the thin alginate layer method was applied to the protoplast culture at an optimal density of 1?×?106 cells per mL??1 and verified the effect of 2,4-D (0.1, 0.5, and 1.0 mg L??1)alone, and 2,4-D (0.5, and 1.0 mg L??1)in combination with BA (0.1 and 0.5 mg L??1)or KN (0.1 and 0.5 mg L??1)on cell division, micro-callus formation. MS medium supplemented with 1.0 mg L??1 2,4-D and 0.1 mg L??1 KN induced optimal cell division, callus formation, and subsequent induction of somatic embryogenesis from the callus. The somatic embryos germinated and converted into plantlets upon transferring to the MS basal medium. This method of Angelica gigas protoplast regeneration can be used for the genetic improvement of this plant.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element ANGELICA GIGAS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PROTOPLAST
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PLANT GROWTH REGULATORS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PLANT REGENERATION
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element SOMATIC EMBRYOGENESIS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element TISSUE CULTURE
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Lee, H. S.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Han, J. E.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Jie, E. Y.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Kim, S. W.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Kwon, H. J.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Lee, G. M.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Park, S. Y.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1URgtWEMpLSF2QKuVSvfH3dkU8pR4GKDb/view?usp=drivesdk">https://drive.google.com/file/d/1URgtWEMpLSF2QKuVSvfH3dkU8pR4GKDb/view?usp=drivesdk</a>
Public note Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
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  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-20952 25.06.2025 25.06.2025 Documentos solicitados