Quantitative relationships for specific growth rates and macromolecular compositions of Mycobacterium tuberculosis, Streptomyces coelicolor A3(2) and Escherichia coli B/r: an integrative theoretical approach.

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 degrees C, and Escherichia coli B/r, grown at 37 degrees C. A frame of reference was established based on quantitative relationships observed between specific growth rates ( micro ) 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 ( micro =0.30 h(-1)) were identified. First, the rate of DNA replication was found to approach the rate reported for E. coli ( micro =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 micro to the number of rrn operons per genome. Values of micro =0.69 h(-1) and micro =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.

[1]  F. Winder,et al.  Effects of nitrogenous components of the medium on the carbohydrate and nucleic acid content of Mycobacterium tuberculosis BCG. , 1970, Journal of general microbiology.

[2]  L. G. Wayne Cultivation of Mycobacterium tuberculosis for Research Purposes , 1994 .

[3]  T. Tønjum,et al.  Differentiation of Mycobacterium ulcerans, M. marinum, and M. haemophilum: Mapping of Their Relationships to M. tuberculosis by Fatty Acid Profile Analysis, DNA-DNA Hybridization, and 16S rRNA Gene Sequence Analysis , 1998, Journal of Clinical Microbiology.

[4]  G. Stent The Operon: On Its Third Anniversary , 1964 .

[5]  M. Nirenberg,et al.  THE IN VITRO FORMATION OF A DNA-RIBOSOME COMPLEX. , 1964, Proceedings of the National Academy of Sciences of the United States of America.

[6]  B. Barrell,et al.  Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2) , 2002, Nature.

[7]  C. Shepard THE EXPERIMENTAL DISEASE THAT FOLLOWS THE INJECTION OF HUMAN LEPROSY BACILLI INTO FOOT-PADS OF MICE , 1960, The Journal of experimental medicine.

[8]  O. Maaløe,et al.  Dependency on medium and temperature of cell size and chemical composition during balanced grown of Salmonella typhimurium. , 1958, Journal of general microbiology.

[9]  C. Arraiano,et al.  Degradation of mRNA in bacteria: emergence of ubiquitous features , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.

[10]  M. J. García,et al.  Restriction fragment length polymorphisms of 16S rRNA genes in the differentiation of fast-growing mycobacterial species. , 1994, FEMS microbiology letters.

[11]  R. Cox,et al.  Effects of Growth Conditions on Expression of Mycobacterial murA and tyrS Genes and Contributions of Their Transcripts to Precursor rRNA Synthesis , 1999, Journal of bacteriology.

[12]  T. Feltwell,et al.  Erratum: Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence , 1998, Nature.

[13]  R. Cox Ribosomes , 1975, Nature.

[14]  S. Oliver,et al.  Growth rate control of protein and nucleic acid content in Streptomyces coelicolor A3(2) and Escherichia coli B/r. , 1996, Microbiology.

[15]  M Grunberg-Manago,et al.  Messenger RNA stability and its role in control of gene expression in bacteria and phages. , 1999, Annual review of genetics.

[16]  O. Kafri,et al.  Mycobacteria possess a surprisingly small number of ribosomal RNA genes in relation to the size of their genome. , 1986, Biochemical and biophysical research communications.

[17]  N. W. Davis,et al.  The complete genome sequence of Escherichia coli K-12. , 1997, Science.

[18]  C. Shepard,et al.  EFFECT OF ENVIRONMENTAL TEMPERATURES ON INFECTION WITH MYCOBACTERIUM MARINUM (BALNEI) OF MICE AND A NUMBER OF POIKILOTHERMIC SPECIES , 1963, Journal of bacteriology.

[19]  R M Harshey,et al.  Rate of ribonucleic acid chain growth in Mycobacterium tuberculosis H37Rv , 1977, Journal of bacteriology.

[20]  V. Chernick A new evolutionary scenario for the Mycobacterium tuberculosis complex. , 2004, Pediatric pulmonology.

[21]  Arkady B. Khodursky,et al.  Global analysis of mRNA decay and abundance in Escherichia coli at single-gene resolution using two-color fluorescent DNA microarrays , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[22]  C. Helmstetter,et al.  DNA synthesis during the division cycle of rapidly growing Escherichia coli B/r. , 1968, Journal of molecular biology.

[23]  Graham R. Stewart,et al.  Tuberculosis: a problem with persistence , 2003, Nature Reviews Microbiology.

[24]  P. D. Hart,et al.  RESPONSE OF CULTURED MACROPHAGES TO MYCOBACTERIUM TUBERCULOSIS, WITH OBSERVATIONS ON FUSION OF LYSOSOMES WITH PHAGOSOMES , 1971, The Journal of experimental medicine.

[25]  T. Hansen Bergey's Manual of Systematic Bacteriology , 2005 .

[26]  F. Neidhardt,et al.  Growth of the bacterial cell , 1983 .

[27]  C. Condon,et al.  Depletion of functional ribosomal RNA operons in Escherichia coli causes increased expression of the remaining intact copies. , 1993, The EMBO journal.

[28]  C. Hoogland,et al.  '98 Escherichia coli SWISS‐2DPAGE database update , 1998, Electrophoresis.

[29]  M. Dreyfus,et al.  Function in Escherichia coli of the non‐catalytic part of RNase E: role in the degradation of ribosome‐free mRNA , 2002, Molecular microbiology.

[30]  A. Khodursky,et al.  Life after transcription--revisiting the fate of messenger RNA. , 2003, Trends in genetics : TIG.

[31]  J. Tyagi,et al.  Mycobacterium tuberculosis rrnPromoters: Differential Usage and Growth Rate-Dependent Control , 1999, Journal of bacteriology.

[32]  M. Chamberlin,et al.  RNA chain initiation by Escherichia coli RNA polymerase. Structural transitions of the enzyme in early ternary complexes. , 1989, Biochemistry.

[33]  J. Pieters,et al.  A Coat Protein on Phagosomes Involved in the Intracellular Survival of Mycobacteria , 1999, Cell.

[34]  G. Woods,et al.  Mycobacteria other than Mycobacterium tuberculosis: review of microbiologic and clinical aspects. , 1987, Reviews of infectious diseases.

[35]  T. Ramakrishnan,et al.  Deoxyribonucleic acid replication time in Mycobacterium tuberculosis H37 Rv , 1986, Archives of Microbiology.

[36]  R. Cox Correlation of the rate of protein synthesis and the third power of the RNA : protein ratio in Escherichia coli and Mycobacterium tuberculosis. , 2003, Microbiology.

[37]  L. Wayne,et al.  An in vitro model for sequential study of shiftdown of Mycobacterium tuberculosis through two stages of nonreplicating persistence , 1996, Infection and immunity.

[38]  C. A. Thomas,et al.  Visualization of Bacterial Genes in Action , 1970, Science.

[39]  C. Condon,et al.  rRNA operon multiplicity in Escherichia coli and the physiological implications of rrn inactivation , 1995, Journal of bacteriology.

[40]  H. Bremer Modulation of Chemical Composition and Other Parameters of the Cell by Growth Rate , 1999 .