Cryopreservation of Arum palaestinum plant callus as a strategy for mitigating extinction risks

Arum palaestinum is a wild perennial plant commonly known as "Al-Loof" in Jordan. Due to overharvesting, climate change, and increasing demand, its natural populations are threatened with extinction. Cryopreservation, an effective method for conserving plant material at ultra-low temperatures, is explored for A. palaestinum calli. We investigated the applicability of encapsulation-vitrification (using different plant vitrification solutions (PVS) and incubation times), encapsulation-dehydration (using sucrose or sorbitol at different concentrations and dehydration times), and the v-cryoplate (using different pre-culture times and temperatures) techniques. In the encapsulation-vitrification experiment, a notable 82.4 % regrowth rate was achieved by desiccating calli in plant vitrification solution 2 (PVS2) for 10 minutes at 25 °C. The encapsulation-dehydration technique resulted in an 82.6 % regrowth rate by incubating calli for one day in low sucrose levels (0.1 M sucrose) following one hour of air dehydration, where the moisture content of the beads was 30 %. The moisture content of the beads decreased from 81 % before chemical and air dehydration to 71 % after 0 hours of air dehydration combined with chemical dehydration using 0.1 M sucrose or sorbitol. It further dropped to 30–34 % after one day of chemical dehydration with 0.1 M sucrose and 1 hour of air dehydration. The v-cryoplate technique successfully conserved calli, showing impressive survival and regrowth percentages (96.8 %) when the callus was pre-cultured with 0.3 M sucrose for three days at 5 °C. Temperature during pre-culture significantly influenced regrowth percentages in the v-cryoplate technique. The study establishes promising cryopreservation protocols for A. palaestinum calli, offering a means to conserve germplasm and contribute to environmental and biodiversity protection by reintroducing endangered plants to their native habitats. • Encapsulation-vitrification with PVS2 achieved high regrowth in Arum palaestinum . • Encapsulation-dehydration with low sucrose led to successful callus regrowth. • V-cryoplate technique significantly enhanced survival and regrowth of calli. • Pre-culture conditions greatly influenced regrowth in the v-cryoplate method. • Cryopreservation methods support conservation of endangered A. palaestinum species.

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Publication Details

Journal
Current Plant Biology
Published
2024-10-18
DOI
https://doi.org/10.1016/j.cpb.2024.100402
Citations
5
Primary Topic
Plant tissue culture and regeneration
Type
article
Field-Weighted Citation Impact
1.17
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article

Cryopreservation of Arum palaestinum plant callus as a strategy for mitigating extinction risks

Sobhia Saifan, Rida A. Shibli, Reham W. Tahtamouni, Tamara S. Al-Qudah et al.
5 citations
Current Plant Biology
Plant tissue culture and regeneration
1.17
article

Cryopreservation of Arum palaestinum plant callus as a strategy for mitigating extinction risks

Sobhia Saifan, Rida A. Shibli, Reham W. Tahtamouni, Tamara S. Al-Qudah, Tamadour Al –Qudah
article en
5 citations

Abstract

Arum palaestinum is a wild perennial plant commonly known as "Al-Loof" in Jordan. Due to overharvesting, climate change, and increasing demand, its natural populations are threatened with extinction. Cryopreservation, an effective method for conserving plant material at ultra-low temperatures, is explored for A. palaestinum calli. We investigated the applicability of encapsulation-vitrification (using different plant vitrification solutions (PVS) and incubation times), encapsulation-dehydration (using sucrose or sorbitol at different concentrations and dehydration times), and the v-cryoplate (using different pre-culture times and temperatures) techniques. In the encapsulation-vitrification experiment, a notable 82.4 % regrowth rate was achieved by desiccating calli in plant vitrification solution 2 (PVS2) for 10 minutes at 25 °C. The encapsulation-dehydration technique resulted in an 82.6 % regrowth rate by incubating calli for one day in low sucrose levels (0.1 M sucrose) following one hour of air dehydration, where the moisture content of the beads was 30 %. The moisture content of the beads decreased from 81 % before chemical and air dehydration to 71 % after 0 hours of air dehydration combined with chemical dehydration using 0.1 M sucrose or sorbitol. It further dropped to 30–34 % after one day of chemical dehydration with 0.1 M sucrose and 1 hour of air dehydration. The v-cryoplate technique successfully conserved calli, showing impressive survival and regrowth percentages (96.8 %) when the callus was pre-cultured with 0.3 M sucrose for three days at 5 °C. Temperature during pre-culture significantly influenced regrowth percentages in the v-cryoplate technique. The study establishes promising cryopreservation protocols for A. palaestinum calli, offering a means to conserve germplasm and contribute to environmental and biodiversity protection by reintroducing endangered plants to their native habitats. • Encapsulation-vitrification with PVS2 achieved high regrowth in Arum palaestinum . • Encapsulation-dehydration with low sucrose led to successful callus regrowth. • V-cryoplate technique significantly enhanced survival and regrowth of calli. • Pre-culture conditions greatly influenced regrowth in the v-cryoplate method. • Cryopreservation methods support conservation of endangered A. palaestinum species.

Current Plant BiologyVol. 40
Al-Ahliyya Amman University (JO), University of Jordan (JO), Mutah University (JO), Al-Balqa Applied University (JO)
Climate action
Openalex Percentile: Top 21%
Plant tissue culture and regeneration
1.17
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