CN102823499B - Blueberry tissue culture seedling factory breeding method - Google Patents

Blueberry tissue culture seedling factory breeding method Download PDF

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CN102823499B
CN102823499B CN201210349632.XA CN201210349632A CN102823499B CN 102823499 B CN102823499 B CN 102823499B CN 201210349632 A CN201210349632 A CN 201210349632A CN 102823499 B CN102823499 B CN 102823499B
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tissue culture
blueberry
seedling
blueberry tissue
medium
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CN102823499A (en
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黄科
刘奕清
汤玲
黄登艳
袁海英
唐建民
陈泽雄
廖林正
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Chongqing University of Arts and Sciences
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Abstract

The invention discloses a factorized breeding method of blueberry (LM3) tissue-cultured seedlings, which is characterized by comprising the step of taking 1/4 MW culture medium as rooting medium, wherein the medium does not contain any hormone including IBA (indolebutyric acid) and NAA (naphthaleneacetic acid). Through the factorized breeding method of the blueberry tissue-cultured seedlings, the seedling rooting rate is up to 100%, and the root systems are strong and have lateral buds, the transplanting survival rate is high and the seedlings are strong and rapid in growth; and the method disclosed by the invention is short in period, low in cost and capable of completely satisfying the demand of large-area cultivation and has favorable application prospect.

Description

蓝莓组培种苗工厂化繁育方法Blueberry tissue culture seedling factory breeding method

技术领域 technical field

本发明涉及一种种苗繁育方法,是一种蓝莓组培种苗工厂化繁育方法。The invention relates to a seedling breeding method, which is an industrial breeding method of blueberry tissue culture seedlings.

背景技术 Background technique

蓝莓(Blueberry)为杜鹃花科(Ericaceae)越橘属(Vaccinium.SPP)灌木类浆果果树,是目前世界上主要的小果类果树之一,具有很高的保健功能,在医药、化妆、食用色素和食品加工等行业具有广泛用途。蓝莓果实除含有一般水果所含的有机酸、维生素和矿物质外,还富含不饱和脂肪酸、鞣花酸和多种生物活性物质,低糖、低脂肪,抗氧化能力居所有果品、蔬菜之首。因而被国际粮农组织列为五大健康食品之一,堪称“世界水果之王”,是近几年来发展最迅速的集营养与保健于一身的第3代果树品种,风靡欧美。Blueberry (Blueberry) is a shrub berry fruit tree of Ericaceae (Ericaceae) Vaccinium.SPP. It is one of the main small fruit fruit trees in the world at present. Industries such as pigments and food processing have a wide range of uses. In addition to the organic acids, vitamins and minerals contained in ordinary fruits, blueberry fruit is also rich in unsaturated fatty acids, ellagic acid and a variety of biologically active substances. It is low in sugar and fat, and its antioxidant capacity ranks first among all fruits and vegetables. . Therefore, it is listed as one of the top five healthy foods by the International Food and Agriculture Organization, and it can be called the "King of Fruits in the World".

我国蓝莓引种工作始于20世纪80年代中期,引种规模日益扩大,种苗生产供不应求。有关蓝莓品种的繁殖和组织培养研究较多,但有关其无根苗诱导生根的研究较少。my country's blueberry introduction work began in the mid-1980s, and the scale of introduction has been expanding day by day, and the supply of seedlings is in short supply. There are many studies on the propagation and tissue culture of blueberry varieties, but few studies on the induced rooting of its unrooted seedlings.

发明内容 Contents of the invention

有鉴于此,本发明的目的在于提供一种蓝莓组培种苗工厂化繁育方法。In view of this, the object of the present invention is to provide a method for factory breeding of blueberry tissue culture seedlings.

为达到此目的,本发明的蓝莓组培种苗工厂化繁育方法,包括以下步骤:To achieve this purpose, the blueberry tissue culture seedling factory breeding method of the present invention comprises the following steps:

(1)生根培养:当继代增殖丛生芽生长至3~5cm高时,将丛生芽切成单芽,转接至生根培养基中在光照条件下进行生根培养,获得试管苗;所述生根培养基以1/4MW培养基作为基本培养基(附表1),并添加浓度为20g/L的蔗糖、浓度为6g/L的卡拉胶,pH为5.8~6.2。(1) rooting culture: when the subculture multiplied clustered buds grow to a height of 3 to 5 cm, the clustered shoots were cut into single buds, transferred to the rooting medium and carried out rooting culture under light conditions to obtain test-tube plantlets; The medium uses 1/4MW medium as the basic medium (attached table 1), and adds sucrose with a concentration of 20g/L and carrageenan with a concentration of 6g/L, and the pH is 5.8-6.2.

(2)试管苗移栽:将步骤(1)所得试管苗移栽入体积比为3∶7的珍珠岩-泥炭土混合基质中培养,即得蓝莓组培种苗。(2) Transplanting test-tube seedlings: transplanting the test-tube seedlings obtained in step (1) into a mixed matrix of perlite-peat moss with a volume ratio of 3:7 for cultivation, to obtain blueberry tissue culture seedlings.

进一步,步骤(1)所述培养温度为25±1℃,光照强度为1500~2500lux,光照时间为每天12~16小时;Further, the cultivation temperature in step (1) is 25±1°C, the light intensity is 1500-2500 lux, and the light time is 12-16 hours per day;

进一步,步骤(1)所述光照强度为1500lux,光照时间为每天12小时;Further, the light intensity described in step (1) is 1500lux, and the light time is 12 hours per day;

进一步,步骤(1)当继代增殖丛生芽生长至3~5cm高时,将丛生芽切成单芽,转接至增殖培养基。Further, step (1) when the subcultured proliferating clustered shoots grow to a height of 3-5 cm, the clustered shoots are cut into single buds and transferred to the proliferation medium.

本发明的有益效果在于:本发明系统地进行了蓝莓生根培养和试管苗移栽等研究工作,建立并优化蓝莓组培种苗工厂化繁育方法:芽苗生根率达100%,根系健壮且有侧芽萌发;移栽成活率高,且芽苗健壮,生长快;本发明方法周期短,成本低,完全能满足大面积规模化栽培的需要,具有良好的应用前景。The beneficial effects of the present invention are: the present invention has systematically carried out research work such as blueberry rooting culture and test-tube seedling transplantation, establishes and optimizes blueberry tissue culture seedling factory breeding method: the rooting rate of sprouts reaches 100%, and the root system is strong and healthy. The side buds germinate; the transplanting survival rate is high, and the sprouts are strong and grow quickly; the method of the invention has short cycle and low cost, can fully meet the needs of large-scale cultivation, and has good application prospects.

附图说明 Description of drawings

为了使本发明的目的、技术方案和优点更加清楚,下面将结合附图对本发明作进一步的详细描述,其中:In order to make the purpose, technical solutions and advantages of the present invention clearer, the present invention will be described in further detail below in conjunction with the accompanying drawings, wherein:

图1蓝莓生根照片Figure 1 Blueberry Rooting Photo

图2蓝莓工厂化繁育照片Figure 2 Photos of blueberry factory breeding

具体实施方式 Detailed ways

以下将参照附图,对本发明的优选实施例进行详细的描述。Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.

本发明以重庆市永川区黄瓜山蓝莓为实验材料,系统地进行了生根培养和试管苗移栽等研究工作,建立并优化了蓝莓组培种苗工厂化繁育方法。The invention takes the Cuguashan blueberry in Yongchuan District, Chongqing City as the experimental material, systematically carries out research work such as rooting culture and test-tube seedling transplantation, and establishes and optimizes the blueberry tissue culture seedling factory breeding method.

1、生根培养基的优化1. Optimization of rooting medium

将继代增殖丛生芽中生长健壮、株高为3~5cm的芽苗转接至5种不同激素浓度配比的生根培养基,在光照条件下进行生根培养,获得试管苗;生根培养基以1/4MW、1/2MW、1/4CQM6、1/2CQM6培养基为基本培养基(基本培养基的配方如表1-4所示)。The sprouts growing vigorously and with a plant height of 3-5 cm from the subcultured proliferating clustered buds were transferred to five rooting media with different hormone concentration ratios, and the rooting culture was carried out under light conditions to obtain test-tube plantlets; the rooting media was 1/4MW, 1/2MW, 1/4CQM6, and 1/2CQM6 medium are basic medium (the formula of basic medium is shown in Table 1-4).

表1生根培养基以1/4MWTable 1 rooting medium with 1/4MW

Figure BSA00000779983100021
Figure BSA00000779983100021

Figure BSA00000779983100031
Figure BSA00000779983100031

表2生根培养基1/2MWTable 2 rooting medium 1/2MW

Figure BSA00000779983100032
Figure BSA00000779983100032

Figure BSA00000779983100041
Figure BSA00000779983100041

表3生根培养基1/4CQM6Table 3 rooting medium 1/4CQM6

表4生根培养基1/2CQM6Table 4 rooting medium 1/2CQM6

Figure BSA00000779983100051
Figure BSA00000779983100051

并添加浓度为0.1mg/LIBA和浓度为0.1mmg/L的NAA作为对照,培养基pH为5.8~6.2;培养温度为25±1℃,光照强度为1500lux,光照时间为每天12小时;观察不同矿质元素和激素浓度配比的生根培养基对蓝莓生根的影响,每种培养基接种芽苗数为90,60天后统计生根数和芽苗生长情况。And add the concentration of 0.1mg/LIBA and the concentration of 0.1mmg/L of NAA as a control, the pH of the medium is 5.8-6.2; the culture temperature is 25±1°C, the light intensity is 1500lux, and the light time is 12 hours a day; observe different The effect of the rooting medium with the concentration ratio of mineral elements and hormones on blueberry rooting. The number of sprouts inoculated with each medium was 90, and the number of roots and the growth of sprouts were counted after 60 days.

结果见表5。由表52可知,蓝莓在1/4MW生根培养基中未加0.1mg/L IBA和浓度为0.1mg/L的NAA的能诱导芽苗生根,当培养基中只加入0.1mg/LIBA和浓度为0.1mg/L的NAA时1/4MW不能诱导芽苗生根;蓝莓在1/4CQM6、1/2CQM6培养基中不能生根。因此,本发明选择1/4MW生根培养基中未加0.1mg/LIBA和浓度为0.1mg/L的NAA的为最优生根培养基。The results are shown in Table 5. It can be seen from Table 52 that blueberries can induce rooting of sprouts without adding 0.1mg/L IBA and NAA with a concentration of 0.1mg/L in the 1/4MW rooting medium. When only 0.1mg/LIBA is added to the medium and the concentration is When 0.1mg/L NAA was used, 1/4MW could not induce sprouts to take root; blueberry could not take root in 1/4CQM6, 1/2CQM6 medium. Therefore, the present invention selects 1/4MW rooting medium without adding 0.1mg/LIBA and NAA with a concentration of 0.1mg/L as the optimal rooting medium.

表5不同培养基及激素浓度配比的生根培养基对蓝莓生根的影响Table 5 Effects of rooting media with different media and hormone concentration ratios on blueberry rooting

Figure BSA00000779983100061
Figure BSA00000779983100061

最后说明的是,以上实施例仅用以说明本发明的技术方案而非限制,尽管通过参照本发明的优选实施例已经对本发明进行了描述,但本领域的普通技术人员应当理解,可以在形式上和细节上对其作出各种各样的改变,而不偏离所附权利要求书所限定的本发明的精神和范围。Finally, it is noted that the above embodiments are only used to illustrate the technical solutions of the present invention and not to limit them. Although the present invention has been described with reference to the preferred embodiments of the present invention, those skilled in the art should understand that it can be described in the form Various changes may be made in matter and details thereof without departing from the spirit and scope of the invention as defined in the appended claims.

Claims (3)

1. the seedling industrialized mating system of blueberry tissue culture kind, is characterized in that: comprise the following steps:
(1) culture of rootage: when the shoot proliferation Multiple Buds of robust growth grows to 3~5cm when high, Multiple Buds is cut into simple bud, is forwarded in root media, carry out culture of rootage under illumination condition, obtain test-tube plantlet; Described root media code is 1/4MW, and specifically the raw material mixed preparing by following mass concentration forms, and this medium does not comprise any hormone of IBA and NAA:
Figure FSB0000114217690000011
(2) test-tube seedling transplanting: it is to cultivate in perlite-peat soil mixed-matrix of 3: 7 that step (1) gained test-tube seedling transplanting is entered to volume ratio, obtains blueberry tissue culture seedling.
2. the seedling industrialized mating system of blueberry tissue culture kind according to claim 1, is characterized in that: step (1) cultivation temperature is 25 ± 1 ℃, and intensity of illumination is 1500~2500lux, and light application time is 12~16 hours every days.
3. the seedling industrialized mating system of blueberry tissue culture kind according to claim 2, is characterized in that: step (1) intensity of illumination is 1500lux, and light application time is 12 hours every days.
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