Low sodium isocyanurate concentrations as a substitute to medium autoclaving in plant tissue culture

An optimization for a medium sterilization method, capable of substituting autoclaving, was developed using low concentrations of sodium isocyanurate (ISO) as a medium sterilizer. Sodium isocyanurate was used in it’s dichloro form (sodium dichloroisocyanurate) with concentrations on medium ranging f...

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Published inPlant cell, tissue and organ culture Vol. 139; no. 3; pp. 601 - 604
Main Authors da Costa Urtiga, Caio, de Araújo Silva-Cardoso, Inaê Mariê, Araujo Figueiredo, Sergio
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.12.2019
Springer Nature B.V
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Abstract An optimization for a medium sterilization method, capable of substituting autoclaving, was developed using low concentrations of sodium isocyanurate (ISO) as a medium sterilizer. Sodium isocyanurate was used in it’s dichloro form (sodium dichloroisocyanurate) with concentrations on medium ranging from 0.04 to 0.005 g/L. The chosen specimen was Dianthus caryophyllus , placed in Murashige and Skoog media as seeds. Sterilization using sodium isocyanurate surpassed that of medium autoclaving on time spent, resources required and sterilization capability. All successful ISO concentrations, 0.04 g/L to 0.01 g/L, allowed D. caryophyllus sprouts to develop with no signs of phytotoxic effects and with constant growth until they reached their container’s maximum capacity. Contamination rates for concentrations 0.04 g/L, 0.02 and 0.01 g/L stayed bellow 5% for the entirety of the experiment. The data presented, along with how this work was conducted, indicate that sodium isocyanurate is capable of substituting media autoclaving for practices with D. caryophyllus seeds and opens a path for further research involving sodium isocyanurate sterilization for other species. Key message This protocol is an optimization for an already existing medium sterilization protocol, in plant tissue culture, through chemical compounds. Sodium isocyanurate was capable of sterilizing culture media in varied concentrations while showing no signs of phytotoxicity to Dianthus caryophyllus seeds and subsequent sprouts.
AbstractList An optimization for a medium sterilization method, capable of substituting autoclaving, was developed using low concentrations of sodium isocyanurate (ISO) as a medium sterilizer. Sodium isocyanurate was used in it’s dichloro form (sodium dichloroisocyanurate) with concentrations on medium ranging from 0.04 to 0.005 g/L. The chosen specimen was Dianthus caryophyllus, placed in Murashige and Skoog media as seeds. Sterilization using sodium isocyanurate surpassed that of medium autoclaving on time spent, resources required and sterilization capability. All successful ISO concentrations, 0.04 g/L to 0.01 g/L, allowed D. caryophyllus sprouts to develop with no signs of phytotoxic effects and with constant growth until they reached their container’s maximum capacity. Contamination rates for concentrations 0.04 g/L, 0.02 and 0.01 g/L stayed bellow 5% for the entirety of the experiment. The data presented, along with how this work was conducted, indicate that sodium isocyanurate is capable of substituting media autoclaving for practices with D. caryophyllus seeds and opens a path for further research involving sodium isocyanurate sterilization for other species.
An optimization for a medium sterilization method, capable of substituting autoclaving, was developed using low concentrations of sodium isocyanurate (ISO) as a medium sterilizer. Sodium isocyanurate was used in it’s dichloro form (sodium dichloroisocyanurate) with concentrations on medium ranging from 0.04 to 0.005 g/L. The chosen specimen was Dianthus caryophyllus , placed in Murashige and Skoog media as seeds. Sterilization using sodium isocyanurate surpassed that of medium autoclaving on time spent, resources required and sterilization capability. All successful ISO concentrations, 0.04 g/L to 0.01 g/L, allowed D. caryophyllus sprouts to develop with no signs of phytotoxic effects and with constant growth until they reached their container’s maximum capacity. Contamination rates for concentrations 0.04 g/L, 0.02 and 0.01 g/L stayed bellow 5% for the entirety of the experiment. The data presented, along with how this work was conducted, indicate that sodium isocyanurate is capable of substituting media autoclaving for practices with D. caryophyllus seeds and opens a path for further research involving sodium isocyanurate sterilization for other species. Key message This protocol is an optimization for an already existing medium sterilization protocol, in plant tissue culture, through chemical compounds. Sodium isocyanurate was capable of sterilizing culture media in varied concentrations while showing no signs of phytotoxicity to Dianthus caryophyllus seeds and subsequent sprouts.
Author Araujo Figueiredo, Sergio
da Costa Urtiga, Caio
de Araújo Silva-Cardoso, Inaê Mariê
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CitedBy_id crossref_primary_10_1590_01047760201925042688
crossref_primary_10_17660_ActaHortic_2023_1359_19
crossref_primary_10_3390_horticulturae8080677
crossref_primary_10_1109_TPS_2022_3214145
crossref_primary_10_2989_20702620_2022_2162459
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ContentType Journal Article
Copyright Springer Nature B.V. 2019
Plant Cell, Tissue and Organ Culture (PCTOC) is a copyright of Springer, (2019). All Rights Reserved.
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Keywords Medium autoclaving
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Snippet An optimization for a medium sterilization method, capable of substituting autoclaving, was developed using low concentrations of sodium isocyanurate (ISO) as...
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crossref
springer
SourceType Aggregation Database
Publisher
StartPage 601
SubjectTerms Autoclaving
Biomedical and Life Sciences
Chemical compounds
Contamination
Culture media
Dianthus caryophyllus
Life Sciences
Low concentrations
Optimization
Organic chemistry
Phytotoxicity
Plant Genetics and Genomics
Plant Pathology
Plant Physiology
Plant Sciences
Plant tissues
Research Note
Seeds
Sodium
Sodium dichloroisocyanurate
Sterilization
Tissue culture
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Title Low sodium isocyanurate concentrations as a substitute to medium autoclaving in plant tissue culture
URI https://link.springer.com/article/10.1007/s11240-019-01681-9
https://www.proquest.com/docview/2300455129
Volume 139
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