百欧博伟生物谈谈亚硝化单胞菌 ATCC BAA-120的培养注意事项
中国微生物菌种查询网 / 2018-08-02 14:32:47

北京百欧博伟生物谈谈 亚硝化单胞菌 ATCC BAA-120的培养注意事项 
Nitrosomonas europaea Winogradsky  菌株拉丁名 
(ATCC? BAA-1201?) 菌株编号
Strain Designations菌株别名: ML1 /
Type Strain 模式菌株: no /
Biosafety Level 生物安全等级 : 1
Strain Designations 菌株别名      ML1
Isolation 分离源 Sludge Wisconsin, United States isolation date: September, 2003
Type Strain 模式菌株no
Biosafety Level 生物安全等级     1
Product Format 提供形式 frozen
Medium 培养基 ATCC? Medium 2265: Nitrosomonas europaea medium
Growth Conditions 生长条件
 Temperature 培养温度 : 30.0℃
Name of Depositor 寄存人 DR Noguera, H Park Special Collection NSF - Bacteriology
Isolation Sludge Wisconsin, United States
isolation date: September, 2003
Year of Origin 收藏年份 2003
References 参考文献 Park HD, Noguera DR. Evaluating the effect of dissolved oxygen on ammonia-oxidizing bacterial communities in activated sludge.. Water Res. 38: 3275-3286, 2004. PubMed: 15276744
chemostat reactor seeded with activated sludge, Marshall wastewater treatment plant, Marshall, WI  
其中开通海外直邮业务专业代理美国ATCC微生物菌种保藏中心菌种细菌和噬菌体(18380)细胞系和杂交瘤(5004);真菌和酵母(58208)
原代细胞(143);原生动物和藻类(2426)
干细胞(102);载体,克隆与分子(18005);病毒(3598)除了专利和受控产品其他均可供应,全方位满足您实验需求,另到货时间短COA齐全。
Medium 培养基 ATCC? Medium 18: Trypticase Soy Agar/Broth
那么培养时间应该注意什么呢?
Propagation Procedure
1.Open vial according to enclosed instructions.
2.From a single tube of #18 broth (5 to 6 ml), withdraw approximately 0.5 to 1.0 ml with a Pasteur or 1.0 ml pipette and use to rehydrate the entire pellet.
3.Use 0.1 ml of this suspension to inoculate #18 slants and 0.1ml to inoculate #18 plates.
4.Incubate tubes and plates at 30oC, under aerobic conditions, for 24 hours.
5.After 24 hours of incubation, wash cells from the slant and transfer this broth to a new slant and plate. Incubate another 24 hours under aerobic conditions. This second transfer and incubation is necessary for complete removal of the cryoprotectant, which can inhibit growth.
1.根据随附的说明打开样品瓶。
2.从#18肉汤(5至6毫升)的单管中,用巴斯德或1.0毫升移液管取出约0.5至1.0毫升,并用于再水化整个颗粒。
3.使用0.1ml该悬浮液接种#18斜面和0.1ml接种#18板。
4.在有氧条件下,在30℃下孵育管和板24小时。
5.孵育24小时后,从斜面洗涤细胞并将该肉汤转移到新的斜面和平板上。 在有氧条件下再孵育24小时。 这种第二次转移和温育对于完全除去可以抑制生长的冷冻保护剂是必需的。

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