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Establishment of an In Vitro Regeneration System for Stem Segments of Blackberry APF-190T
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Shuaishuai Feng1, Feng Qiao1, Aihua Li1, Xuan He2, Tingting Jiang1, Wei Han1, Quanxi Li1, Ailing Huang1, Jin Liu3, Deyun Tan1, *
Chinese Bulletin of Botany | 2026, 61(1) : 136 - 145
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Chinese Bulletin of Botany | 2026, 61(1): 136-145
• TECHNIQUES AND METHODS •
Establishment of an In Vitro Regeneration System for Stem Segments of Blackberry APF-190T
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Shuaishuai Feng1, Feng Qiao1, Aihua Li1, Xuan He2, Tingting Jiang1, Wei Han1, Quanxi Li1, Ailing Huang1, Jin Liu3, Deyun Tan1, *
Affiliations
  • 1Zibo Academy of Agricultural Sciences, Zibo 255033, China
  • 2Zhoucun District Agricultural and Rural Bureau, Zibo 255090, China
  • 3Shandong Agriculture and Engineering University, Zibo 255300, China
Published: 2026-01-10 doi: 10.11983/CBB25027
Outline
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INTRODUCTION:

Blackberry (Rubus fruticosus) is an important economic crop whose fruits are not only rich in fiber, vitamins, and phenolic metabolites, but also have significant health benefits. Traditional blackberry propagation methods, including seed propagation, layering, cutting, and suckering, have various limitations. For example, seed propagation has a long cycle, a low germination rate, and variable offspring traits. In contrast, tissue culture-based rapid propagation technology offers distinct advantages, such as season-independent operation, a high multiplication coefficient, and preservation of superior maternal traits, making it an effective solution for blackberry plantlet propagation. Therefore, it is necessary to establish an efficient blackberry rapid propagation system, which would lay the foundation for large-scale production of high-quality virus-free plantlets and germplasm innovation.

RATIONALE:

The establishment of an in vitro regeneration system for blackberry stem segments is based on the theory of plant cell totipotency and hormonal regulatory mechanisms, under which the meristematic cells of stem segments can regenerate into complete plants under suitable culture conditions. To establish a stable regeneration system for blackberry APF-190T, we investigated the effects of sterilization conditions, medium types, and the types and concentrations of plant growth regulators on primary culture, proliferation culture, and rooting culture. Additionally, the influence of different substrates on the growth of tissue-cultured plantlets was further analyzed.

RESULTS:

Comparative experiments on disinfection durations revealed that a 7-minute treatment yielded optimal results for blackberry explants, with the lowest contamination rate of 20.00%, a relatively low browning rate of 6.67%, and the highest survival rate of 73.33%. In MS media, these conditions produced the best stem segment growth, with a maximum bud induction rate of 63.33%, characterized by abundant germinated buds reaching an average length of 1.41 cm. For primary culture, the combination of 1.0 mg∙L–1 6-BA+0.2 mg∙L–1 NAA was the most effective, achieving a 100% bud induction rate and producing robust seedlings with dark green leaves. Subsequent proliferation culture with a combination of 0.8 mg∙L–1 6-BA and 0.1 mg∙L–1 NAA resulted in the highest adventitious bud proliferation coefficient of 12.51 and the tallest average bud height of 3.83 cm, along with vigorous growth. The rooting efficiency peaked in 1/2MS medium supplemented with 1.0 mg∙L–1 NAA, attaining a 97.78% rooting rate with an average of 5.11 thick roots per plant, featuring well-developed lateral roots and abundant fine roots. Finally, transplantation success was maximized when a 2:1 (v/v) peat-vermiculite substrate was used, resulting in a 95.56% survival rate with robust plant growth, expanded leaves, and continuous root development.

CONCLUSION:

For in vitro propagation of blackberry stem explants, the optimal sterilization protocol was achieved using 75% ethanol for 30 s followed by 2% sodium hypochlorite for 7 min. For primary culture, the most suitable medium was MS+1.0 mg∙L–1 6-BA+0.2 mg∙L–1 NAA. For shoot proliferation, the best results were obtained with MS+0.8 mg∙L–1 6-BA+0.1 mg∙L–1 NAA, promoting optimal shoot multiplication. During the rooting stage, the highest rooting efficiency was observed in the 1/2MS+1.0 mg∙L–1 NAA group. For ex vitro acclimatization, a peat mixture proved most effective for seedling survival and growth under controlled greenhouse conditions, and this technique can potentially be applied for commercialization of the plant.

blackberry  /  explant  /  tissue culture  /  proliferation culture
冯帅帅, 乔峰, 李爱花, 何璇, 姜婷婷, 韩葳, 李全希, 黄爱玲, 刘进, 谭德云. 黑莓APF-190T茎段离体再生体系的建立. 植物学报, 2026 , 61 (1) : 136 -145 . DOI: 10.11983/CBB25027
Shuaishuai Feng, Feng Qiao, Aihua Li, Xuan He, Tingting Jiang, Wei Han, Quanxi Li, Ailing Huang, Jin Liu, Deyun Tan. Establishment of an In Vitro Regeneration System for Stem Segments of Blackberry APF-190T[J]. Chinese Bulletin of Botany, 2026 , 61 (1) : 136 -145 . DOI: 10.11983/CBB25027
Year 2026 volume 61 Issue 1
142
67
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doi: 10.11983/CBB25027
  • Receive Date:2025-02-20
  • Online Date:2026-10-15
  • Published:2026-01-10
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  • Received:2025-02-20
  • Accepted:2025-06-03
Affiliations
    1Zibo Academy of Agricultural Sciences, Zibo 255033, China
    2Zhoucun District Agricultural and Rural Bureau, Zibo 255090, China
    3Shandong Agriculture and Engineering University, Zibo 255300, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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