|本期目录/Table of Contents|

[1]张婷婷,马磊.枯草杆菌启动子P43及Pamy的转录活性[J].江苏农业科学,2014,42(12):56-58.
 Zhang Tingting,et al.Transcriptional activity of Bacillus subtilis promoter P43 and Pamy[J].Jiangsu Agricultural Sciences,2014,42(12):56-58.
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枯草杆菌启动子P43及Pamy的转录活性(PDF)
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《江苏农业科学》[ISSN:1002-1302/CN:32-1214/S]

卷:
第42卷
期数:
2014年12期
页码:
56-58
栏目:
生物技术
出版日期:
2014-12-25

文章信息/Info

Title:
Transcriptional activity of Bacillus subtilis promoter P43 and Pamy
作者:
张婷婷 马磊
石河子大学生命科学学院,新疆石河子 832000
Author(s):
Zhang Tingtinget al
关键词:
枯草杆菌启动子转录活性基因表达
Keywords:
-
分类号:
Q933
DOI:
-
文献标志码:
A
摘要:
利用报告基因β-半乳糖苷酶,分析了枯草杆菌启动子P43及Pamy的转录活性。结果表明,在基本培养基条件下,启动子P43在对数前期开始表现转录活性,随菌量增大活性迅速提高,稳定期逐步平稳;在富营养培养基条件下,启动子P43转录活性在对数前期与基本培养基条件下相似,在对数期转录活性增加速率则高于基本培养基条件下的增加速率;启动子P43转录活性在E. coliB. subtilis体内基本一致。启动子Pamy在淀粉诱导下转录活性较高,在添加葡萄糖以及无诱导条件下酶活较低。
Abstract:
-

参考文献/References:

[1]徐友强,马翠卿,陶飞,等. 细菌启动子识别及应用研究进展[J]. 生物工程学报,2010,26(10):1393-1403.
[2]Wang P Z,Doi R H. Overlapping promoters transcribed by Bacillus subtilis sigma 55 and sigma 37 RNA polymerase holoenzymes during growth and stationary phases[J]. Journal of Biological Chemistry,1984,259(13):8619-8625.
[3]Blombach B, Eikmanns B J. Current knowledge on isobutanol production with Escherichia coliBacillus subtilis and Corynebacterium glutamicum[J]. Bioengineered,2011,2(6):346-350.
[4]Lu Y P,Lin Q,Wang J,et al. Overexpression and characterization in Bacillus subtilis of a positionally nonspecific lipase from Proteus vulgaris[J]. Journal of Industrial Microbiology & Biotechnology,2010,37(9):919-925.
[5]Harwood C R,Cutting S M. Molecular biological methods for Bacillus:vol. 707[M]. New York:Wiley,1990.
[6]Ye R Q,Kim J H,Kim B G,et al. High evel secretory production of intact,biologically active staphylokinase from Bacillus subtilis[J]. Biotechnology and Bioengineering,1999,62(1):87-96.
[7]Lin X,Wong S L,Miller E S,et al. Expression of the bacillus licheniformis PWD-1 keratinase gene in B. subtilis[J]. Journal of Industrial Microbiology and Biotechnology,1997,19(2):134-138.
[8]Yang S,Huang H,Zhang R,et al. Expression and purification of extracellular penicillin G acylase in Bacillus subtilis[J]. Protein Expression and Purification,2001,21(1):60-64.
[9]Stülke J,Hillen W. Regulation of Carbon catabolism in Bacillus species[J]. Annual Review of Microbiology,2000,54(1):849-880.
[10]Braaz R,Wong S L,Jendrossek D. Production of PHA depolymerase A(PhaZ5)from Paucimonas lemoignei in Bacillus subtilis[J]. FEMS Microbiology Letters,2002,209(2):237-241.
[11]Gat O,Inbar I,Aloni-Grinstein R,et al. Use of a promoter trap system in Bacillus anthracis and Bacillus subtilis for the development of recombinant protective antigen-based vaccines[J]. Infection and Immunity,2003,71(2):801-813.

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备注/Memo

备注/Memo:
收稿日期:2014-01-08
基金项目:国家自然科学基金(编号:31272416);石河子大学高层次人才科研启动专项(编号:RCZX201137);石河子大学优秀青年项目(编号:2012ZRKXYQ13);石河子大学青年骨干教师培养计划。
作者简介:张婷婷(1984—),硕士,讲师,从事微生物生态研究。E-mail:120978935@qq.com。
通信作者:马磊,博士,副教授,从事生物信息学与分子遗传研究。E-mail:mlei@shzu.edu.cn。
更新日期/Last Update: 2014-12-25