RNA polymerases from low G+C gram-positive bacteria

被引:3
作者
Miller, Michael [1 ]
Oakley, Aaron J. [1 ]
Lewis, Peter J. [1 ,2 ,3 ]
机构
[1] Univ Newcastle, Sch Environm & Life Sci, Callaghan, NSW 2308, Australia
[2] Univ Wollongong, Sch Chem & Mol Biosci, Wollongong, NSW, Australia
[3] Illawarra Hlth & Med Res Inst, Wollongong, NSW, Australia
来源
TRANSCRIPTION-AUSTIN | 2021年 / 12卷 / 04期
基金
澳大利亚研究理事会;
关键词
RNA polymerase; Transcription regulation; Low G+C bacteria; Auxiliary factors; Antibiotics; SUBTILIS DELTA-FACTOR; N-TERMINAL DOMAIN; BACILLUS-SUBTILIS; TRANSCRIPTION INITIATION; STRUCTURAL BASIS; SUBUNIT-OMEGA; COMPLEX; INHIBITORS; REGULATOR; BINDING;
D O I
10.1080/21541264.2021.1964328
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The low G + C Gram-positive bacteria represent some of the most medically and industrially important microorganisms. They are relied on for the production of food and dietary supplements, enzymes and antibiotics, as well as being responsible for the majority of nosocomial infections and serving as a reservoir for antibiotic resistance. Control of gene expression in this group is more highly studied than in any bacteria other than the Gram-negative modela Escherichia coli, yet until recently no structural information on RNA polymerase (RNAP) from this group was available. This review will summarize recent reports on the high-resolution structure of RNAP from the model low G + C representativea Bacillus subtilis, including the role of auxiliary subunits i ' and i mu, and outline approaches for the development of antimicrobials to target RNAP from this group.
引用
收藏
页码:92 / 102
页数:11
相关论文
共 71 条
  • [1] Structural Basis of Transcription: RNA Polymerase Backtracking and Its Reactivation
    Abdelkareem, Mo'men
    Saint-Andre, Charlotte
    Takacs, Maria
    Papai, Gabor
    Crucifix, Corinne
    Guo, Xieyang
    Ortiz, Julio
    Weixlbaumer, Albert
    [J]. MOLECULAR CELL, 2019, 75 (02) : 298 - +
  • [2] Narrow-Spectrum Antibacterial Agents-Benefits and Challenges
    Alm, Richard A.
    Lahiri, Sushmita D.
    [J]. ANTIBIOTICS-BASEL, 2020, 9 (07):
  • [3] Novel synthetic molecules targeting the bacterial RNA polymerase assembly
    André, E
    Bastide, L
    Michaux-Charachon, S
    Gouby, A
    Villain-Guillot, P
    Latouche, J
    Bouchet, A
    Gualtiéri, M
    Leonetti, JP
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (02) : 245 - 251
  • [4] Mutational analysis of β′260-309, a σ70 binding site located on Escherichia coli core RNA polymerase
    Arthur, TM
    Anthony, LC
    Burgess, RR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (30) : 23113 - 23119
  • [5] Ayres DL, 2012, SYST BIOL, V61, P170, DOI [10.1093/sysbio/sys029, 10.1093/sysbio/syr100]
  • [6] Phage T7 Gp2 inhibition of Escherichia coli RNA polymerase involves misappropriation of σ70 domain 1.1
    Bae, Brian
    Davis, Elizabeth
    Brown, Daniel
    Campbell, Elizabeth A.
    Wigneshweraraj, Sivaramesh
    Darst, Seth A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (49) : 19772 - 19777
  • [7] Local and global regulation of transcription initiation in bacteria
    Browning, Douglas F.
    Busby, Stephen J. W.
    [J]. NATURE REVIEWS MICROBIOLOGY, 2016, 14 (10) : 638 - 650
  • [8] CDC, 2013, CTR DIS CONTR
  • [9] 6S RNA Mimics B-Form DNA to Regulate Escherichia coli RNA Polymerase
    Chen, James
    Wassarman, Karen M.
    Feng, Shili
    Leon, Katherine
    Feklistov, Andrey
    Winkelman, Jared T.
    Li, Zongli
    Walz, Thomas
    Campbell, Elizabeth A.
    Darst, Seth A.
    [J]. MOLECULAR CELL, 2017, 68 (02) : 388 - +
  • [10] Protein-protein interactions as antibiotic targets: A medicinal chemistry perspective
    Cossar, Peter J.
    Lewis, Peter J.
    McCluskey, Adam
    [J]. MEDICINAL RESEARCH REVIEWS, 2020, 40 (02) : 469 - 494