次培养基

基本解释 (translations)

subcultures

与次培养基相关的网络例句 [注：此内容来源于网络，仅供参考]

3H］-TdR incorporation rate was used as an index of cell proliferation. Additionally, we investigated whether the ASMC proliferative responses to SP were modulated by preincubation for 2 h with GR71251, a specific antagonist of NK-1 receptor, and neomycin, a phospholipase C inhibitor, and nitrendipine, a blockader of Ca2+ channel, respectively.

细胞增殖实验研究：将平滑肌细胞以1×103/孔接种在96孔板内，含10% FCS-DMEM培养24 h，吸去上清，以无血清DMEM洗涤2次，加入该培养基培养48 h，同步化之后以无血清培养基继续培养48 h或分别加入含SP(10-7～10-5 mol/L)和NK-1受体激动剂［Sar9，Met(O2)11］-SP(10-7～10-5 mol/L)的无血清DMEM培养相同时间。

Methods①The minimum inhibitory concentration and the minimum fungicidal concentration of citral against C.

方法①参照NCCLS M27A方案中的微量液基稀释法测定柠檬醛和氟康唑对原始白念珠菌的最低抑菌浓度和最低杀菌浓度；②采用多步诱导法，观察在含梯度浓度(1～50MIC)柠檬醛培养基上连续转种的白念珠菌MIC的变化情况，以氟康唑作为阳性对照，同时设空白对照和溶媒对照；③将敏感性下降的诱导株在无药培养基上连续转种10次后，检测其MIC值；④测定柠檬醛对氟康唑敏感性下降诱导株的MIC值。

In conclusion, the lag phase of Streptococcus thermophilus was shorten in the eutrophy culture medium, and the time achieving the culminated point of logarithmic phase was shorted also, at the same time, the stationary phase lengthened. After secondary culture, Streptococcus thermophilus reached directly the log phase hardly through the lag phase, and then quickly reached the decline phase. There were more relations of the metabolic regalities of the three kinds of nutritive substances with the super-concentrated incubation process of Streptococcus thermophilus: the more the number of the bacteria, the quicker the metaboling, while the fewer, the slower the metabolism. Moreover, there apparently existed morphologic changes in this course, and there maybe existed the apoptosis, which correlated with bacteria propagation and acid producing. With the culture time postponed, the nutritive substances in the culture medium lacked also, and the morphologic change and apoptosis appeared more obviously.

结果表明，嗜热链球菌在营养丰富的培养基中的生长延滞期缩短，到达对数生长顶点的时间变短，稳定期的时间延长，当经过二次培养后，嗜热链球菌几乎不经过延滞期直接到达对数期，平稳期持续的时间较短，很快到达衰亡期；嗜热链球菌在超浓缩培养过程中三大营养物质的代谢规律也同它的培养过程有很大的关系，菌数多，其代谢旺盛，菌数降低其代谢速度减慢；嗜热链球菌在超浓缩培养过程中存在着明显的菌体形态变化，并可能存在着细胞凋亡，与菌体增殖和产酸规律密切相关，随着培养时间延长，培养基中营养物质变得贫乏，菌体形态变化和细胞凋亡的情况愈加明显。

The result indicated:① In accordance with culturing in the medium containing MS, SH, N6 macroelement, respectively, the effect of MS or SH macroelement in the primary culture is better than that of N6 macroelement, and the effect based on N6 macroelement is the best from 5th to 9th subculture.

结果表明：①在含MS、SH、N6的大量元素的培养基上的初代培养，MS或SH的效果好于N6，愈伤组织第5~9次继代培养中，N6大量元素培养基的继代培养效果最好。

Culture tender leaves in culture medium of MS+2,4-D1.5mg/L+30g/L suger+0.7% agar pH5.8 for 20 days in darkness at 25℃, and then subculture to induced Ⅱ-type calli. Use forceps cutting the tissue to nubble with 2mm2, and put the tissue into Agrodacterium tumefaciens LBA4404 liquid supplemented with AS 100mg/L,then, co-culture 3 days, resume 7 days in MS+2,4-D1.5mg/L+30g/L suger+500mg/L cef, take to MS+2,4-D1.5mg/L+30g/L suger+100mg/L cef+10.0mg/L kanamycin culture 20 days in darkness. After that to make it polarize in MS+30g/L suger+100mg/L cef+10.0mg/L km. The percentage of km resistant callus was reached max after infection for 45 min, the average is 29.66%. Simultaneity, tender leave callus are infected 5 min by A. tumefaciens liquid in different negative pressure, and kept on 15 min in Agrodacterium tumefaciens liquid without negative pressure. Then screen out resistant callus and obtain transgenic plants. When the negative pressure is -0.05MP the percentage of km resistant callus was reached max, the average rate is 37.5%.

将心叶接种于MS+2.4-D1.5mg/L+30g/L 蔗糖，琼脂0.7%，pH5.8 培养基中25℃暗培养20d 后继代一次，诱导产生Ⅱ型胚性愈伤组织，用镊子将其夹碎成2mm2大小的小块，置入添加100mg/L AS 的根癌农杆菌LBA4404 菌液中，侵染时间为45min，共培养3 天后，转入MS+2.4-D1.5mg/L+30g/L 蔗糖+500mg/L Cef 培养基中恢复7天，再转入MS+2.4-D1.5mg/L+30g/L 蔗糖+100mg/L Cef+10.0mg/L Km 中，遮光培养20d后，置入其MS+30g/L 蔗糖+100mg/L Cef+10.0mg/L Km 分化，卡那霉素抗性愈伤组织获得率在侵染45min 时达到最大值平均为29.66%；同时以甘蔗心叶愈伤组织材料，通过循环水式真空泵，产生负压，设定不同的负压值，在农杆菌菌液中感染5min 后，在负压条件下继续侵染15min 后，筛选出抗性愈伤组织并获得转化植株，其中在负压为-0.05 时转化率达到最大值，其卡那霉素抗性愈伤组织获得率平均为37.5%。

The medium-Nitsch basic medium with 1umol/L 2, 4-D was suitable for the growth of somatic cells. The trimness degree of somatic embryogenesis was more improved after the treatments of cells to be sifted with 1mm diameter screen in 4 days of subculture.

胚性细胞团悬浮培养最适培养基为ND培养基，在继代后4天将细胞团经孔径1mm的钢质筛网多次过滤处理，可以使体细胞胚胎发生的整齐度大大增强。

The growth of Ficus carica test-tube seedlings on MS media was sharply inhibited by NaCl with lethal in 300 mmolL^(-1) NaCl and, in leaf, dramatical increase in sodium content and K(superscript +)/Na(superscript +) ratio, in addition to proline and soluble sugar accumulation in 0~200 mmolL^(-1) NaCl.

将多次继代培养的无花果试管苗接种在含NaCl不同浓度的MS培养基上，300mmolL^(-1)NaCl使试管苗致死。在0~200mmolL^(-1)NaCl的培养基上，试管苗生长显著受到抑制，叶片中Na含量增加，K/Na上升。

Plantlet regeneration from cotyledon of Citrullus lanatus cv. Zhangkang No. 4 was studied. The results showed that aseptic seedlings should be cultured in dark for 3d, then exposed to a photoperiod of 16/8h/d for 3d. The callus induction rate was higher in cotyledons placed facing downwards to the medium than in those facing upwards. The highest induction rate occurred in MS medium containing 6-BA (2.0mg/L), kinetin (1.0mg/L)and GA3 (1.0mg/L). The induction initiated in dark and took 7 days, while callus growth and differentiation proceeding for 7 days under 16/8h light-dark cycles. A highest rate of embryogenic callus was obtained after 3 successive subcultures.

以无子西瓜郑抗4号无菌苗子叶为外植体，进行了体细胞胚发生及植株再生的研究，结果表明，无菌苗应先进行3d暗培养，然后采取光照16h/d和黑暗8h/d培养3d；将子叶的叶面朝下放置于培养基上的愈伤组织诱导率高于叶面朝上的培养方式；子叶诱导胚性愈伤组织的最适培养基配方为MS+6-BA2.0mg/L+KT1.0mg/L+GA31.0mg/L；诱导需要在黑暗条件下启动，进行7d暗培养，而生长分化于光照16h/d和黑暗8h/d条件下培养7d；继代3次得到的胚性愈伤组织最多；最适生根培养基配方为1/2MS+IBA0.3mg/L。

A research of the cultivation treatments of the commonly used compost fermentations on Volvariella Volvacea production was made in this paper by comparison with the cultivation of raw ingredients. They are zymotechnics of water-logged compost, twice regular zymotechnics and simple twice zymotechnics. The result shows that the cultivation effects of above three are better than that of the cultivation of raw ingredients, among which the simple twice zymotechnics is the best.

研究草菇生产中常用的培养基发酵方法，以生料栽培为对照，采用自然堆沤发酵法、常规二次发酵法和简易二次发酵法对草菇栽培的影响，调查结果表明：自然堆沤发酵法、常规二次发酵法和简易二次发酵法的栽培效果都要优于对照，其中，效果最好的是简易二次发酵法。

Albicans strains with fluconazole. Method: A series of 16 strains C. albicans from the same body were induced to form pseudo-hyphae in RPMI 1640 medium and DMEM medium at 37 癈 for twenty-four hours respectively. The pseudo-hyphae and yeast were counted and the ratio between pseudo-hypha and total cells was calculated. C. albicans strains were induced to form pseudo-hyphae in RPMI 1640 medium for seven days by transferring twelve times. The genome DNAs of the hyphal-form of C. albicans was cleaved by two restriction enzymes EcoR I and Bgl II, the products were electrophored and photoed.

以同一母体来源的白念珠菌CA-1～A-17(共16株)作为研究对象，采用RPMI1640和DMEM培养基，37℃培养24h诱导其假菌丝形成，记录不同观察时间时的菌丝相和酵母相细胞数，计算菌丝相白念珠菌形成率；以RPMI1640培养基，37℃连续传代培养7天(转种12次)后，分离菌丝相白念珠菌并提取其基因组DNA；以EcoRⅠ和BglⅡ消化菌丝相基因组DNA，消化产物进行琼脂糖凝胶电泳并拍照；用随机引物(5'…TCACCACGGT…3')扩增菌丝相基因组DNA，采用变性聚丙烯酰胺凝胶电泳分离扩增产物并拍照。

与次培养基相关的网络解释 [注：此内容来源于网络，仅供参考]

diploid：双倍体

第三阶段是减数分裂,双倍体(diploid)细胞核经过两次连续的分裂,形成四个单倍体的核(N),从而回到原来的单倍体阶段. 经过有性生殖,真菌可产生四种类型的有性孢子. 配方一 萨市(Sabouraud's)培养基

mycobacteria：分枝杆菌

但培养14天和进行肉汤末次接种会更有效. 当临床症状提示为弗朗西丝菌(Francisella)感染时,阳性血液培养物需要接种到BCYE琼脂培养基,所有操作应在生物安全三级的层流罩超净台中进行. 3、 分枝杆菌(Mycobacteria) 使用常规血培养基不能分离.

subcool：过冷

subcontrary 小反对关系的 | subcool 过冷 | subculture 次培养基

triple sulphonamide suspension：三磺嘧啶悬液

triple sugar medium 三糖培养基 | triple sulphonamide suspension 三磺嘧啶悬液 | triple superheterodyne 三次变频超外差接收机

incubating fifty eggs at one time：一次孵五十个鸡蛋

incrusted soil ==> 结壳土壤 | incubating fifty eggs at one time ==> 一次孵五十个鸡蛋 | incubation media ==> 培养基

thymidine：胸腺嘧啶核苷

选择培养基具有3种关键成分:次黄嘌呤(hypoxanthine)、氨甲蝶呤(aminopterin)和胸腺嘧啶核苷(thymidine),故名HAT培养基. 这个培养基通过抑制瘤细胞的核苷酸合成,达到去除未融合瘤细胞的目的. 细胞有两条基本途径合成嘌呤核苷酸,