Zhou Yangyan, Li Qing, Wang Zejia, Zhang Yue
School of Advanced Agricultural Sciences, Peking University, Beijing 100871, China.
Key Research Institute of Yellow River Civilization and Sustainable Development & Collaborative Innovation Center on Yellow River Civilization, Henan University, Kaifeng 475001, China.
Life (Basel). 2023 Jan 15;13(1):242. doi: 10.3390/life13010242.
The main propagation approach is tissue culture in blueberries, and tissue culture is an effective and low-cost method with higher economic efficiency in blueberries. However, there is a lack of stable and efficient production systems of industrialization of tissue culture in blueberries. In this study, the high-efficiency tissue culture and rapid propagation technology system were established based on blueberry leaves and stems. The optimal medium for callus induction was WPM (woody plant medium) containing 2.0 mg/L Forchlorfenuron (CPPU), 0.2 mg/L 2-isopentenyladenine (2-ip) with a 97% callus induction rate and a callus differentiation rate of 71% by using blueberry leaves as explants. The optimal secondary culture of the leaf callus medium was WPM containing 3.0 mg/L CPPU with an increment coefficient of 24%. The optimal bud growth medium was WPM containing 1.0 mg/L CPPU, 0.4 mg/L 2-ip, with which the growth of the bud was better, stronger and faster. The optimal rooting medium was 1/2 Murashige and Skoog (1/2MS) medium containing 2.0 mg/L naphthylacetic acid (NAA), with which the rooting rate was 90% with shorter rooting time and more adventitious root. In addition, we established a regeneration system based on blueberry stems. The optimal preculture medium in blueberry stem explants was MS medium containing 2-(N-morpholino) ethanesulfonic acid (MES) containing 0.2 mg/L indole-3-acetic acid (IAA), 0.1 mg/L CPPU, 100 mg/L NaCl, with which the germination rate of the bud was 93%. The optimal medium for fast plant growth was MS medium containing MES containing 0.4 mg/L zeatin (ZT), 1 mg/L putrescine, 1 mg/L spermidine, 1 mg/L spermidine, which had a good growth state and growth rate. The optimal cultivation for plantlet growth was MS medium containing MES containing 0.5 mg/L isopentene adenine, with which the plantlet was strong. The optimal rooting medium for the stem was 1/2MS medium containing 2.0 mg/L NAA, with which the rooting rate was 93% with a short time and more adventitious root. In conclusion, we found that stem explants had higher regeneration efficiency for a stable and efficient production system of industrialization of tissue culture. This study provides theoretical guidance and technical support in precision breeding and standardization and industrialization in the blueberry industry.
蓝莓的主要繁殖方式是组织培养,组织培养是一种有效且低成本的方法,在蓝莓中具有较高的经济效益。然而,蓝莓组织培养缺乏稳定高效的产业化生产体系。本研究基于蓝莓叶片和茎建立了高效组织培养与快速繁殖技术体系。以蓝莓叶片为外植体,愈伤组织诱导的最佳培养基是含有2.0mg/L氯吡脲(CPPU)、0.2mg/L 2-异戊烯基腺嘌呤(2-ip)的WPM(木本植物培养基),愈伤组织诱导率为97%,愈伤组织分化率为71%。叶片愈伤组织继代培养的最佳培养基是含有3.0mg/L CPPU的WPM,增殖系数为24%。最佳芽生长培养基是含有1.0mg/L CPPU、0.4mg/L 2-ip的WPM,在此培养基上芽生长更好、更强、更快。最佳生根培养基是含有2.0mg/L萘乙酸(NAA)的1/2Murashige和Skoog(1/2MS)培养基,生根率为90%,生根时间短且不定根多。此外,我们还建立了基于蓝莓茎的再生体系。蓝莓茎外植体的最佳预培养基是含有2-(N-吗啉代)乙磺酸(MES)、0.2mg/L吲哚-3-乙酸(IAA)、0.1mg/L CPPU、100mg/L氯化钠的MS培养基,芽萌发率为93%。快速植株生长的最佳培养基是含有MES、0.4mg/L玉米素(ZT)、1mg/L腐胺、1mg/L亚精胺的MS培养基,生长状态和生长速率良好。植株生长的最佳培养基是含有MES、0.5mg/L异戊烯腺嘌呤的MS培养基,在此培养基上植株健壮。茎的最佳生根培养基是含有2.0mg/L NAA的1/2MS培养基,生根率为9