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探讨箭叶芋体外再生模式的组织学和分子见解。

Histological and molecular insights in to in vitro regeneration pattern of Xanthosoma sagittifolium.

机构信息

Tissue Culture and Cryopreservation Unit, ICAR- National Bureau of Plant Genetic Resources (NBPGR), New Delhi, 110012, India.

Sam Higgimbottom University of Agriculture and Technology, Prayagraj, UP, India.

出版信息

Sci Rep. 2023 Apr 10;13(1):5806. doi: 10.1038/s41598-023-33064-8.

DOI:10.1038/s41598-023-33064-8
PMID:37037867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10086020/
Abstract

A study on the effect of various phytohormonal combinations on in vitro propagation of Cocoyam [Xanthosoma sagittifolium (L.) Schott] was conducted to develop an improved and efficient in vitro regeneration protocol for its mass multiplication. Histological analysis to understand the in vitro regeneration pattern and genetic fidelity assessment of regenerated plants were also carried out. Single shoots excised from in vitro established cultures of X. sagittifolium were used as explants. Among the 32 different phytohormonal combinations tested, indirect organogenesis with intervening callus phase was observed on majority of the media combinations. Meristematic clump formation was optimally achieved on all the tested media combinations with maximum 43.54 ± 0.51 shoot primordia on MS medium containing 0.2 mg/L BAP + 0.1 mg/L NAA followed by 36.44 ± 0.76 shoot primordia on MS medium having 2.5 mg/L TDZ. Micro-morphological analysis of different morphogenetic structures revealed that the regeneration of cocoyam is well executed via meristematic nodules, shoot primordia formation that may evolve in to proper shoots. Adventitious shoots (> 2 cm) were successfully (100.00 ± 0.00%) rooted on the half-strength MS medium containing IBA (0.05-1.0 mg/L) and IAA (0.05-0.5 mg/L). The number of roots ranged from 0.78 ± 0.31 on the control half-strength MS medium to 13.94 ± 0.46 on half-strength MS supplemented with 1.0 mg/L IBA. Considering somaclonal variations as a potential restriction to in vitro multiplication of plants, genetic stability was assessed using 40 ISSR primers. The PCR amplification profiles obtained from all the tested propagules (calli, meristematic clumps, regenerated plantlets) were similar to the mother plants indicating the homogeneity of the individuals raised through the regeneration protocol reported here.

摘要

开展了一项关于不同植物激素组合对芋(Xanthosoma sagittifolium(L.)Schott)离体繁殖影响的研究,旨在开发一种改进和高效的离体再生方案,以实现其大量繁殖。还进行了组织学分析,以了解体外再生模式和再生植物的遗传保真度评估。从芋离体培养的单芽中切取外植体。在所测试的 32 种不同植物激素组合中,观察到大多数培养基组合均发生间接器官发生,并伴有中间愈伤组织阶段。在所有测试的培养基组合中,分生组织丛的形成达到最佳状态,在含有 0.2mg/L BAP+0.1mg/L NAA 的 MS 培养基上获得最大的 43.54±0.51 个芽原基,其次是在含有 2.5mg/L TDZ 的 MS 培养基上获得 36.44±0.76 个芽原基。对不同形态发生结构的微观形态分析表明,芋的再生是通过分生组织结节和芽原基形成来完成的,这些芽原基可能进一步发育成正常的芽。不定芽(>2cm)在含有 IBA(0.05-1.0mg/L)和 IAA(0.05-0.5mg/L)的半强度 MS 培养基上成功生根(100.00±0.00%)。生根数量从对照半强度 MS 培养基上的 0.78±0.31 个到添加 1.0mg/L IBA 的半强度 MS 培养基上的 13.94±0.46 个不等。考虑到体细胞变异可能限制植物的离体繁殖,使用 40 个 ISSR 引物评估遗传稳定性。从所有测试的繁殖体(愈伤组织、分生组织丛、再生苗)获得的 PCR 扩增图谱与母株相似,表明通过这里报道的再生方案获得的个体具有同质性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/c616bdc11285/41598_2023_33064_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/ae909a0b2cdd/41598_2023_33064_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/dfafea91827b/41598_2023_33064_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/761a0f98902b/41598_2023_33064_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/af94091af04e/41598_2023_33064_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/6d36c1396790/41598_2023_33064_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/c616bdc11285/41598_2023_33064_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/ae909a0b2cdd/41598_2023_33064_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/dfafea91827b/41598_2023_33064_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/761a0f98902b/41598_2023_33064_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/af94091af04e/41598_2023_33064_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/6d36c1396790/41598_2023_33064_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eab/10086020/c616bdc11285/41598_2023_33064_Fig6_HTML.jpg

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