The effect of a disrupted yhjQ gene on cellular morphology and cell growth in Escherichia coli

被引:13
作者
Kim, MK
Park, SR
Cho, SJ
Lim, WJ
Ryu, SK
An, CL
Hong, SY
Park, YW
Kahng, GG
Kim, JH
Kim, H
Yun, HD [1 ]
机构
[1] Gyeongsang Natl Univ, Div Appl Life Sci, Chinju 660701, South Korea
[2] Gyeongsang Natl Univ, Res Inst Life Sci, Chinju 660701, South Korea
[3] Kyoto Univ, Wood Res Inst, Gene Express Lab, Uji, Kyoto 611, Japan
[4] Sunchon Natl Univ, Dept Agr Chem, Sunchon 540742, South Korea
基金
新加坡国家研究基金会;
关键词
D O I
10.1007/s00253-002-1102-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The 5' upstream region of the cellulose synthase operon (bcs operon) has been isolated by cloning from Escherichia coli. A gene encoding YhjQ is located 1.0 kb upstream of the bcs operon in E. coli. The function of YhjQ remains unknown. Insertional inactivation of the yhjQ gene causes abnormal cell division, resulting in incomplete partition of the chromosome and filamentous cells of various sizes. These results suggest that the product of yhjQ may affect normal doubling and cellular morphology. Salmonella enteritidis, and Escherichia coli strains also produce cellulose (Zogaj et al. 2001). This multicellularity is a common behavior of bacteria at certain developmental stages, offering strategic advantages in comparison with single cells (Shapiro 1998). Here, we report the cloning of the yhjQ gene that exists in the upstream region of the bcs operon involved in cellulose synthesis in E. coli. Insertional inactivation of this gene hinders cell division, and results in filamentous cells of various sizes.
引用
收藏
页码:134 / 138
页数:5
相关论文
共 19 条
[1]   Structural and putative regulatory genes involved in cellulose synthesis in Rhizobium leguminosarum bv. trifolii [J].
Ausmees, N ;
Jonsson, H ;
Höglund, S ;
Ljunggren, H ;
Lindberg, M .
MICROBIOLOGY-UK, 1999, 145 :1253-1262
[2]   Site-specific recombination of bacteriophage P22 does not require integration host factor [J].
Cho, EH ;
Nam, CE ;
Alcaraz, R ;
Gardner, JF .
JOURNAL OF BACTERIOLOGY, 1999, 181 (14) :4245-4249
[3]   Disruption of a gene encoding a putative γ-butyrolactone-binding protein in Streptomyces tendae affects nikkomycin production [J].
Engel, P ;
Scharfenstein, LL ;
Dyer, JM ;
Cary, JW .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2001, 56 (3-4) :414-419
[5]   REPLACEMENT AND AMPLIFICATION OF BACTERIAL GENES WITH SEQUENCES ALTERED INVITRO [J].
GUTTERSON, NI ;
KOSHLAND, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (16) :4894-4898
[6]   IDENTIFICATION OF A NOVEL RESPONSE REGULATOR REQUIRED FOR THE SWARMER-TO-STALKED-CELL TRANSITION IN CAULOBACTER-CRESCENTUS [J].
HECHT, GB ;
NEWTON, A .
JOURNAL OF BACTERIOLOGY, 1995, 177 (21) :6223-6229
[7]   CHROMOSOME PARTITIONING IN ESCHERICHIA-COLI - NOVEL MUTANTS PRODUCING ANUCLEATE CELLS [J].
HIRAGA, S ;
NIKI, H ;
OGURA, T ;
ICHINOSE, C ;
MORI, H ;
EZAKI, B ;
JAFFE, A .
JOURNAL OF BACTERIOLOGY, 1989, 171 (03) :1496-1505
[8]  
HOFLICH G, 1995, MICROBIOL RES, V150, P139, DOI 10.1016/S0944-5013(11)80048-0
[9]  
JOACHIM F, 1985, GENE, V36, P143
[10]   METHOD FOR DETERMINING WHETHER A GENE OF ESCHERICHIA-COLI IS ESSENTIAL - APPLICATION TO THE POLA GENE [J].
JOYCE, CM ;
GRINDLEY, NDF .
JOURNAL OF BACTERIOLOGY, 1984, 158 (02) :636-643