植物组织培养的培养基包括

2025-02-25 20:52:02
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培养基的配制 植物组织培养中常用的一种培养基是MS培养基。MS培养基的配制包括以下步骤。

培养基母液的配制和保存 MS培养基含有近30种营养成分,为了避免每次配制培养基都要对这几十种成分进行称量,可将培养基中的各种成分,按原量的20倍或200倍分别称量,配成浓缩液,这种浓缩液叫做培养基母液。这样每次使用时,取其总量的1/20(50 mL)或1/200(5 mL),加水稀释,制成培养液。现将制备培养基母液所需的各类物质的量列出,供配制时使用。

大量元素(母液Ⅰ) mg/L

NH4NO3 33 000

KNO3 38 000

CaCl2·2H2O 8 800

MgSO4·7H2O 7 400

KH2PO4 3 400

微量元素(母液Ⅱ)

KI 166

H3BO3 1 240

MnSO4·4H2O 4 460

ZnSO4·7H2O 1 720

Na2MoO4·2H2O 50

CuSO4·5H2O 5

CoCl2·6H2O 5

铁盐(母液Ⅲ)

FeSO4·7H2O 5 560

Na2-EDTA·2H2O 7 460

有机成分(母液Ⅳ)

ⅣA

肌醇 20 000

ⅣB

烟酸 100

盐酸吡哆醇(维生素B6) 100

盐酸硫胺素(维生素B1) 100

甘氨酸 400

以上各种营养成分的用量,除了母液Ⅰ为20倍浓缩液外,其余的均为200倍浓缩液。

上述几种母液都要单独配成1 L的贮备液。其中,母液Ⅰ、母液Ⅱ及母液Ⅳ的配制方法是:每种母液中的几种成分称量完毕后,分别用少量的蒸馏水彻底溶解,然后再将它们混溶,最后定容到1 L。

母液Ⅲ的配制方法是:将称好的FeSO4·7H2O和Na2-EDTA·2H2O分别放到450 mL蒸馏水中,边加热边不断搅拌使它们溶解,然后将两种溶液混合,并将pH调至5.5,最后定容到1 L,保存在棕色玻璃瓶中。

各种母液配完后,分别用玻璃瓶贮存,并且贴上标签,注明母液号、配制倍数、日期等,保存在冰箱的冷藏室中。

MS培养基中还需要加入2,4-二氯苯氧乙酸(2,4-D)、萘乙酸(NAA)、6-苄基嘌呤(6BA)等植物生长调节物质,并且分别配成母液(0.1 mg/mL)。其配制方法是:分别称取这3种物质各10 mg,将2,4-D和NAA用少量(1 mL)无水乙醇预溶,将6BA用少量(1 mL)的物质的量浓度为0.1 mol/L的NaOH溶液溶解,溶解过程需要水浴加热,最后分别定容至100 mL,即得质量浓度为0.1 mg/mL的母液。

配制培养液 用量筒或移液管从各种母液中分别取出所需的用量:母液Ⅰ为50 mL,母液Ⅱ、Ⅲ、ⅣA和ⅣB各5 mL。再取2,4-D 5 mL、NAA 1 mL,与各种母液一起放入烧杯中。

配制培养液时应注意:①在使用提前配制的母液时,应在量取各种母液之前,轻轻摇动盛放母液的瓶子,如果发现瓶中有沉淀、悬浮物或被微生物污染,应立即淘汰这种母液,重新进行配制;②用量筒或移液管量取培养基母液之前,必须用所量取的母液将量筒或移液管润洗2次;③量取母液时,最好将各种母液按将要量取的顺序写在纸上,量取1种,划掉1种,以免出错。

溶化琼脂 用粗天平分别称取琼脂9 g、蒸糖30 g,放入1 000 mL的搪瓷量杯中,再加入蒸馏水750 mL,用电炉加热,边加热边用玻璃棒搅拌,直到液体呈半透明状。然后再将配好的混合培养液加入到煮沸的琼脂中,最后加蒸馏水定容至1 000 mL,搅拌均匀。

需要注意的是,在加热琼脂、制备培养基的过程中,操作者千万不能离开,否则沸腾的琼脂外溢,就需要重新称量、制备。此外,如果没有搪瓷量杯,可用大烧杯代替。但要注意大烧杯底的外表面不能沾水,否则加热时烧杯容易炸裂,使溶液外溢,造成烫伤。

调pH 用滴管吸取物质的量浓度为1 mol/L的NaOH溶液,逐滴滴入溶化的培养基中,边滴边搅拌,并随时用精密的pH试纸(5.4~7.0)测培养基的pH,一直到培养基的pH为5.8为止(培养基的pH必须严格控制在5.8)。

培养基的分装 溶化的培养基应该趁热分装。分装时,先将培养基倒入烧杯中,然后将烧杯中的培养基倒入锥形瓶(50 mL或100 mL)中。注意不要让培养基沾到瓶口和瓶壁上。锥形瓶中培养基的量约为锥形瓶容量的1/5~1/4。每1 000 mL培养基,可分装25~30瓶。

培养基分装完毕后,应及时封盖瓶口。用2块硫酸纸(每块大小约为9 cm×9 cm)中间夹1层薄牛皮纸封盖瓶口,并用线绳捆扎。最后在锥形瓶外壁贴上标签。

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