平板培养

用平板培养法建立生物被膜细菌体外模型；

In-vitro biological envelope models of PA were established by plate cultivation method .

利用平板培养结合PCR-DGGE技术监测酸性电解水对虾的杀菌效果。

Plate culture method combined with PCR-DGGE was applied to monitor the bactericidal efficacy of acidic electrolyzed water on shrimp .

细胞增殖实验结果显示在种植后第3天和第6天，ACP/PLLA材料组和平板培养组的细胞数量明显多于PLLA材料组（P＜0.05）。

The cell proliferation assay showed that the cell number in ACP / PLLA group and monolayer group was much higher than that in PLLA group ( P0.05 ) at 3 and 6 days .

方法用改良平板培养法在硅胶膜上建立铜绿假单胞菌BF模型。

Methods An in vitro model of Pseudomonas aeruginosa bacterial biofilm was established in silicon disk with modified flat board method and a rapid staining procedure of AgNO 3 was used to verify it .

通过子实体组织分离的菌种，接种于PDA和MEA平板培养基上，在25℃恒温下培养1～6周。

By isolating the fructification tissue , the cultures were inoculated in petri dishes on PDA medium and MEA medium , they were incubated at 25 ℃ for 1 ~ 6 weeks .

利用传统的平板培养与DGGE相结合的技术手段，研究了接种AM真菌对番茄根际土壤中的青枯菌和细菌群落结构的影响。

Useing traditional plate culture and DGGE techniques , influence of AM fungal inoculation on Ralstonia solanacearum population and bacterial community structure in tomato rhizosphere were investigated .

通过Biolog微平板培养法我们看到白酒发酵阶段样品微生物活性随培养时间的延长而提高。

With analysis by the Biolog method we observed the microbial activity in samples of different liquor fermentation stages increased with the prolonged incubation time .

首先对系统中富集的PAOs进行平板培养，分析了其传统可培养性低的原因，提出增效剂添加法。

First , PAOs are plate cultured and the reason why PAOs are hard to culture is analyzed . Synergistic agent additive process is introduced .

对9株发酵乳球菌菌株进行MRS固体平板培养基划线分离和形态学比较观察，并采用生化试验和RAPD对其进行鉴定。

In this paper , the isolation and identification of 9 lactic acid coccus strains from fermented milk were studied . The lactic acid bacteria were isolated by MRS plate streaking cultivation and morphological observation , and were identified by biochemical essay and RAPD technique .

将高温驯化选育出的HS-5菌株于分离平板培养。

Isolated plates were used to culture HS-5 which was screened out by high-temperature domestication .

利用稀释平板培养法从连云港地区的土壤中分离了一株苏云金芽孢杆菌新菌株GGD-4，通过PCR-RFLP鉴定体系和SDS-PAGE方法分析了此菌株中cry基因类型和表达蛋白。

In this study , cry-type genes from a new Bacillus thuringiensis GGD-4 stain , isolated by dilution-plate method from Lianyungang , had been identified using PCR-RFLP identification system , and SDS-PAGE analysis and bioassay had been performed .

结果表明：As-1在含硒平板培养基中，当硒含量达5μg/ml时菌丝生长几乎不受抑制；

The results showed that in the solid media , the fungus-AS-1 growth was hardly inhibited when the concentration of sodiun selenite was 5 μ g / ml.

研究结果表明，在固体平板培养基上，菌株M1的生长速度较快；在液体发酵过程中，菌株M1发酵液的滤纸纤维素酶、漆酶和多酚氧化酶的活性均高于其它4个菌株。

The results indicated that growth rate of rhizomorphs of strain M_1washigher than others in the solid medium , and the activation of cellulase , laccase , polyphenol oxidase from strain M_1were higher than that of the other strains in liquid culture .

将培养好的菌液平铺于含有抗生素和X-gal、IPTG的平板培养基中，通过抗药性筛选及蓝白斑试验挑选所需的大肠杆菌，继续于液体培养基中过夜培养。

The bacterio-liquid was spreaded on the plate culture medium contained the Aminobenzylpenicillin , the X-gal and IPTG . ⑦ Then , we picked out the needed germs by drug-resistance screening and the blue-white spots test .

方法用罗氏固体平板培养基，分别采集医院内中央空调控温区、分体空调控温区和无空调区的空气标本，经36.5℃培养28d。

Methods The air-samples in the areas with central air-condition , and independent air-condition and no air-condition were collected and incubated in the Lowenstein-Jensen culture medium separately . The air-samples have been cultivated in 36.5 ℃ for 28 days .

平板培养法和双层培养基法结果表明，HY96-2对Nb-1具有较好的拮抗作用，其抑制率分别为20.1%和24.7%。

Result showed that the inhibition rates were 20.1 % and 24.7 % by dual culture and double layer culture methods , respectively .

在平板培养时，培养25d菌落直径达72.25mm，在发酵培养过程中，在最佳产糖期发酵液中粗多糖含量达7.800mg·ml－1，而对照分别为48.63mm和5.200mg·ml－1。

The contents of their crude polysaccharides in fermenting liquors were up to 7.800 mg · ml - 1 in the highest polysaccharides producing stage . The diameter of colony and the contents of crude polysaccharides are 48.63 mm and 5.200 mg · ml - 1 respectively in the control .

松乳菇菌丝体固体平板培养的研究

Study on fruit body of lactarius deliciosus upon solid culture medium

方法：采用平板培养法、发酵培养法。

METHODS : We cultured Polyporus umbellatus by plate and fermentation respectively .

草珊瑚单细胞克隆的平板培养

Plate culture of single cell clone from Sarcandra glabra

红豆杉单细胞平板培养的研究

Study on the Monocell Plate Culture of Taxus Chinensis

通过平板培养计数法，验证了该配方的杀菌效果。

Its inhibitory effect was confirmed with the method of colony counting on plate .

本文采用平板培养法研究蜂王浆的抗菌活性，发现新鲜蜂王浆对10种试验菌均有不同程度的抑制作用。

Flat culture medium was adopted to study the antibacterial action of bee royal jelly .

在平板培养中，长光照能促进菌落生长和产孢；

During the plate culture , long photoperiods apparently favored the colony growth and sporulation ;

方法用无菌棉拭子取咽后壁分泌物接种于血平板培养。

Method Secretion taken from posterior pharyngeal wall was planted on blood plate for bacterial culture .

平板培养菌落有皱纹，可形成假菌丝。

Cultured by malt extract solid medium , plate colony surface had wrinkle , and could form pseudomycelium .

文中描述了它们在察氏平板培养基上25℃恒温培养3星期的菌落特征。

In this paper , their colony characteristics on Czapek medium under 25 C for 3 weeks were described .

用平板培养及小细胞团培养两种方法筛选高产花青素的玫瑰茄细胞系。

High production anthocyanin roselle cell lines were selected by both single cell clone plate culture and small-cell-aggregate culture .

红花细胞克隆的条件培养的植板率是普通平板培养的3.6倍。

The PE of single cell clones in condition culture was 3.6 times as high as in normal plate culture .

在平板培养基、液体培养基内分别处理这些微生物，蘑菇菌丝体生长速度加快，菌丝量增加。

Adding these microbes into PDA solid and liquid media , the growth rate and biomass of mycelium were increased .