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蓝莓叶片和茎段的高效再生体系

High Efficiency Regeneration System from Blueberry Leaves and Stems.

作者信息

Zhou Yangyan, Li Qing, Wang Zejia, Zhang Yue

机构信息

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.

出版信息

Life (Basel). 2023 Jan 15;13(1):242. doi: 10.3390/life13010242.

Abstract

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.

摘要

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

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d786/9861610/e2f83bed62cc/life-13-00242-g001.jpg

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