基本培养基

在液体基本培养基上，四种菌的生长速率和最大生物量有细微差异，但生物量都在1OD上下。

In liquid minimal medium , the growth rate and the maximum biomass of the four strains have subtle differences .

由于遗传互补，从回交后代构建的异核体能在基本培养基上生长。

Heterokaryons constructed from the the progeny of the final cross are able to grow in minimal medium because of genetic complementation .

邓恩桉继代的最佳基本培养基是改良MS培养基。

MS medium is the best medium for Eucalyptus dunni to subculture .

最适于愈伤组织分化的基本培养基是MS；

The optimal medium for callus differentiation is MS medium ;

结果：以MS培养基为基本培养基，附加BA0.5~1.0mg。

Result : The MS medium with 0.5-1.0 mg .

初代培养中最适基本培养基是MS培养基。

The optimal culture medium in the beginning culture phase is MS medium .

诱导试管苗叶片产生不定芽及对不定芽的生长最适宜的基本培养基是MS；

The best basis medium for adventitious buds induction and growth is MS ;

不同基本培养基对籼稻粤泰A与粤泰B成熟胚愈伤组织诱导及继代的影响

Effects of Different Basic Substrate on Callus Inducing and Successive Transfer Culture for Indica Rice Yue-Tai A and Yue-Tai B

MS是比较适合愈伤组织增殖的基本培养基。

Medium MS did good to callus proliferation .

MS是外植体的适宜基本培养基类型。

MS was the optimum medium type .

结果表明，以离体去皮根段为外植体，MS为基本培养基，诱导愈伤组织较为适宜。

Callus was efficiently induced from in vitro root segment devoid of rhizodermis on MS medium .

分化、扩繁、壮苗培养基为MS基本培养基附加K和IAA。

Differentiation and multiplication and strengthening shoot medium is MS with K and IAA .

MS和1/2MS相比，MS是试管苗生长的最佳基本培养基。

Compared with 1 / 2 MS medium , MS is better for the growth of tube-seedling .

以MS为基本培养基、一品红花序轴为外植体，通过不同植物生长调节剂，诱导不同品种愈伤组织的发生。

The Inflorescence axis of different varieties Euphorbia pulcherrima were used as explants to induce callus proliferation .

以MS为基本培养基，添加一定量的植物细胞分裂素和生长素，进行12个桑品种的叶片培养。

The leaves from 12 mulberry varieties were cultured on medium MS adding with cytokinin and somatotropin .

以MS作为基本培养基，离体培养千头菊带腋芽茎段。

Stem segments of Chrysanthemum morifolium with axillary bud were cultured in vitro on base MS medium .

与MS（1/2N）和1/2MS相比，MS基本培养基更有利于组培苗早期继代增殖。

Compared with MS ( 1 / 2N ), MS basal medium was more beneficial to forepart subculture micropropagation .

试验材料对不同基本培养基具有选择性，NM培养基对水稻种胚愈伤组织诱导有较好的适应性；

Basic media were selected in mature embryo culture . NM medium was adaptable better to callus induction .

以MS（蔗糖3%、琼脂0.8%、pH值5.8）培养基为基本培养基。

With MS ( sucrose 3 % , agar 0.8 % , pH 5.8 ) culture medium as the basic medium .

生长健壮的不定芽和再生植株能在无激素的MS基本培养基上生根。

The health adventitious buds and regen - erated shoots could be rooted on growth regula - tor-free MS medium .

结果表明，籼稻愈伤组织在MS较NB基本培养基上更有利于分化；

For the calli of indica rice MS medium was better than NB medium for explant regeneration ;

小叶品种为材料，用由MS基本培养基配制的25%海藻酸钠包裹腋芽节段（固化剂为25%CaC12），制作人工种子。

Were encapsulated with 2 & 5 % sodium alginate ( Plus a basal MS medium ) for preparating artificial seeds .

以MS为基本培养基，试验探讨了两种不同的激素组合对猕猴桃试管苗形态发生的影响，对组织培养中试管苗形态发生的激素效应作了初步研究。

Taking MS as basic media , we studied the effect of two combination of hormones on morphosis of kiwifruit tube-seedling .

以菊花珍品绿牡丹的茎段为外植体，MS为基本培养基，进行了离体培养。

Tissue culture of chrysanthemum Curiosa-Green peony was carried through using MS as the basic medium and stem sects as explants .

从田间选取甘薯优良品种12份，采用MS基本培养基进行无菌试管苗培养。

The explants of 12 superior sweetpotato cultivars were selected from field and cultured on MS medium to obtain sterile cuttings .

以大叶黄杨带腋芽茎段为材料，以MS和1/2MS为基本培养基，进行组织培养研究。

Euonymus japonica us stem segment with axillary 's bud was cultured with MS and 1 / 2MS medium in this experiment .

以茎尖为外植体，采用MS培养基为基本培养基，适当调整激素浓度，进行白网纹草丛生芽诱导技术及外植体消毒技术研究。

Stem-point is used as explant . And medium MS is used as basic medium . Concentration of internal secretion is adjusted properly .

以马铃薯大西洋品种力材料，MS为基本培养基，研究硅对马铃薯组培苗根系生长及其细胞壁组成的影响。

The growth of potato plantlet was accelerated when cultured in MS_based medium containing H4SiO4.The plantlet was taller and stronger with darker leaves .

以CC培养基作为共培养后抗性愈伤筛选的基本培养基有利于抗性愈伤组织的筛选培养。

The CC medium was an efficient selectable medium for screening hygromycin resistant calli after co cultivation .

而再分化成配子体却比高等植物容易，甚至移入不含激素的MS基本培养基即可形成正常的配子体。

The redifferentiation and regeneration of thalli were far easier than those of higher plants even if they were transplanted onto MS phytohormone-free medium .