Characteristics of fed-batch cultures of recombinant Escherichia coli containing human-like collagen cDNA at different specific growth rates

2005 ◽  
Vol 27 (12) ◽  
pp. 865-870 ◽  
Author(s):  
Dai D Fan ◽  
Yane Luo ◽  
Yu Mi ◽  
Xiao X Ma ◽  
Longan Shang
1988 ◽  
Vol 66 (2) ◽  
pp. 187-191 ◽  
Author(s):  
Norio Shimizu ◽  
Shinichi Fukuzono ◽  
Kiyoshi Fujimori ◽  
Nabuko Nishimura ◽  
Yoji Odawara

2010 ◽  
Vol 45 (8) ◽  
pp. 1334-1341 ◽  
Author(s):  
Juan-Miguel Puertas ◽  
Jordi Ruiz ◽  
Mónica Rodríguez de la Vega ◽  
Julia Lorenzo ◽  
Glòria Caminal ◽  
...  

Microbiology ◽  
2004 ◽  
Vol 150 (5) ◽  
pp. 1413-1426 ◽  
Author(s):  
Robert A. Cox

Further understanding of the physiological states of Mycobacterium tuberculosis and other mycobacteria was sought through comparisons with the genomic properties and macromolecular compositions of Streptomyces coelicolor A3(2), grown at 30 °C, and Escherichia coli B/r, grown at 37 °C. A frame of reference was established based on quantitative relationships observed between specific growth rates (μ) of cells and their macromolecular compositions. The concept of a schematic cell based on transcription/translation coupling, average genes and average proteins was developed to provide an instantaneous view of macromolecular synthesis carried out by cells growing at their maximum rate. It was inferred that the ultra-fast growth of E. coli results from its ability to increase the average number of rRNA (rrn) operons per cell through polyploidy, thereby increasing its capacity for ribosome synthesis. The maximum growth rate of E. coli was deduced to be limited by the rate of uptake and consumption of nutrients providing energy. Three characteristic properties of S. coelicolor A3(2) growing optimally (μ=0·30 h−1) were identified. First, the rate of DNA replication was found to approach the rate reported for E. coli (μ=1·73 h−1); secondly, all rrn operons were calculated to be fully engaged in precursor-rRNA synthesis; thirdly, compared with E. coli, protein synthesis was found to depend on higher concentrations of ribosomes and lower concentrations of aminoacyl-tRNA and EF-Tu. An equation was derived for E. coli B/r relating μ to the number of rrn operons per genome. Values of μ=0·69 h−1 and μ=1·00 h−1 were obtained respectively for cells with one or two rrn operons per genome. Using the author's equation relating the number of rrn operons per genome to maximum growth rate, it is expected that M. tuberculosis with one rrn operon should be capable of growing much faster than it actually does. Therefore, it is suggested that the high number of insertion sequences in this species attenuates growth rate to still lower values.


1992 ◽  
pp. 192-194
Author(s):  
Shinji Sakamoto ◽  
Kazumasa Tsuji ◽  
Kyoko Uehara ◽  
Michiko Aoki ◽  
Ichiro Terada ◽  
...  

2009 ◽  
Vol 14 (5) ◽  
pp. 559-564 ◽  
Author(s):  
Jung Hun Kim ◽  
Seon-Won Kim ◽  
Do Quynh Anh Nguyen ◽  
He Li ◽  
Sung Bae Kim ◽  
...  

2013 ◽  
Vol 13 (4) ◽  
pp. 1056-1062 ◽  
Author(s):  
Saeid Rezaeinejad ◽  
Volodymyr Ivanov

The physiological differences of individual cells of bacterial population may imply the existence of cell subpopulations with different sensitivity to chlorine, which may affect the efficiency of drinking water disinfection. The susceptibility of individual bacterial cells to chlorine was examined using flow cytometry. The inactivation of Escherichia coli cells by chlorine in the populations with specific growth rates of 0.2 and 0.9 h−1 was assessed using various viability indicators. Viability of bacterial cells was evaluated using membrane integrity propidium iodide (PI) dye, respiratory activity indicator of 5-cyano-2,3-ditolyl tetrazolium chloride (CTC) and membrane potential probe of DiBAC4(3). It was found that there were cell subpopulations of E. coli with different levels of susceptibility to chlorine. E. coli cell population with higher specific growth rate was more susceptible to chlorine. The CT values for inactivation of 99% of cells (CT99) in populations of E. coli with specific growth rates of 0.9 and 0.2 h−1 were 0.06 and 0.09 mg min l−1, respectively. Flow cytometry could be used to study the sensitivity of bacterial cells to the chemical agents.


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