The renaissance of continuous culture in the post-genomics age

The development of continuous culture techniques 60 years ago and the subsequent formulation of theory and the diversification of experimental systems revolutionised microbiology and heralded a unique period of innovative research. Then, progressively, molecular biology and thence genomics and related high-information-density omics technologies took centre stage and microbial growth physiology in general faded from educational programmes and research funding priorities alike. However, there has been a gathering appreciation over the past decade that if the claims of systems biology are going to be realised, they will have to be based on rigorously controlled and reproducible microbial and cell growth platforms. This revival of continuous culture will be long lasting because its recognition as the growth system of choice is firmly established. The purpose of this review, therefore, is to remind microbiologists, particularly those new to continuous culture approaches, of the legacy of what I call the first age of continuous culture, and to explore a selection of researches that are using these techniques in this post-genomics age. The review looks at the impact of continuous culture across a comprehensive range of microbiological research and development. The ability to establish (quasi-) steady state conditions is a frequently stated advantage of continuous cultures thereby allowing environmental parameters to be manipulated without causing concomitant changes in the specific growth rate. However, the use of continuous cultures also enables the critical study of specified transition states and chemical, physical or biological perturbations. Such dynamic analyses enhance our understanding of microbial ecology and microbial pathology for example, and offer a wider scope for innovative drug discovery; they also can inform the optimization of batch and fed-batch operations that are characterized by sequential transitions states.

[1]  Jean-Marc Daran,et al.  Exploring and dissecting genome-wide gene expression responses of Penicillium chrysogenum to phenylacetic acid consumption and penicillinG production , 2009, BMC Genomics.

[2]  P. V. van Bodegom,et al.  Microbial Maintenance: A Critical Review on Its Quantification , 2007, Microbial ecology.

[3]  M. Wilcox,et al.  Effects of Exposure of Clostridium difficile PCR Ribotypes 027 and 001 to Fluoroquinolones in a Human Gut Model , 2008, Antimicrobial Agents and Chemotherapy.

[4]  W. Babel The Auxiliary Substrate Concept: From simple considerations to heuristically valuable knowledge , 2009 .

[5]  Eric Werner,et al.  All systems go , 2007, Nature.

[6]  J. Grover,et al.  Element content of Pseudomonas fluorescens varies with growth rate and temperature: A replicated chemostat study addressing ecological stoichiometry , 2008 .

[7]  Matthias Reuss,et al.  In vivo dynamics of glycolysis in Escherichia coli shows need for growth‐rate dependent metabolome analysis , 2008, Biotechnology progress.

[8]  A. C. R. Dean,et al.  Continuous culture 6. Applications and new fields. , 1976 .

[9]  J. van der Greef,et al.  The art and practice of systems biology in medicine: mapping patterns of relationships. , 2007, Journal of proteome research.

[10]  Matthew R. Johnson,et al.  Genome-Wide Transcriptional Variation within and between Steady States for Continuous Growth of the Hyperthermophile Thermotoga Maritima , 2005, Applied and Environmental Microbiology.

[11]  D. Metzgar,et al.  Development of a novel continuous culture device for experimental evolution of bacterial populations , 2007, Applied Microbiology and Biotechnology.

[12]  Christine Klockow,et al.  Transcriptional response of the model planctomycete Rhodopirellula baltica SH1T to changing environmental conditions , 2009, BMC Genomics.

[13]  J. Pronk,et al.  Chemostat-based micro-array analysis in baker's yeast. , 2009, Advances in microbial physiology.

[14]  W. Babel,et al.  Mixed Substrate Utilization in Micro-organisms: Biochemical Aspects and Energetics , 1985 .

[15]  A. Bull,et al.  The physiology and metabolic control of fungal growth. , 1977, Advances in microbial physiology.

[16]  David G. Russell,et al.  Tuberculosis: What We Don’t Know Can, and Does, Hurt Us , 2010, Science.

[17]  M. Penttilä,et al.  Transcriptional monitoring of steady state and effects of anaerobic phases in chemostat cultures of the filamentous fungus Trichoderma reesei , 2006, BMC Genomics.

[18]  Ismo Mattila,et al.  On-line monitoring of continuous beer fermentation process using automatic membrane inlet mass spectrometric system. , 2005, Talanta.

[19]  D. Harrison Physiological effects of dissolved oxygen tension and redox potential on growing populations of micro-organisms , 1972 .

[20]  A. Bull Microbial Diversity and Bioprospecting , 2003 .

[21]  H. Jannasch,et al.  Mixed Culture Studies with the Chemostat , 1972 .

[22]  D. Hoyle,et al.  Identification and characterization of high-flux-control genes of yeast through competition analyses in continuous cultures , 2008, Nature Genetics.

[23]  T. Lyons,et al.  Directed evolution of a filamentous fungus for thermotolerance , 2009, BMC biotechnology.

[24]  Hongjuan Zhao,et al.  Manipulation of the physiology of clavulanic acid biosynthesis with the aid of metabolic flux analysis , 2006 .

[25]  A. Novick,et al.  Description of the chemostat. , 1950, Science.

[26]  Jean-Marc Daran,et al.  Exploiting combinatorial cultivation conditions to infer transcriptional regulation , 2007, BMC Genomics.

[27]  J. McFadden,et al.  Compiling a Molecular Inventory for Mycobacterium bovis BCG at Two Growth Rates: Evidence for Growth Rate-Mediated Regulation of Ribosome Biosynthesis and Lipid Metabolism , 2005, Journal of bacteriology.

[28]  T. Horiuchi [Continuous culture of bacteria]. , 1972, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[29]  P. Silver,et al.  1 Why We Need Systems Biology , 2006 .

[30]  J. Elser,et al.  Ecological Stoichiometry: The Biology of Elements from Molecules to the Biosphere , 2002 .

[31]  K. Flynn Use, abuse, misconceptions and insights from quota models — the Droop cell quota model 40 years on , 2008 .

[32]  J. Lennon,et al.  Rapid evolution buffers ecosystem impacts of viruses in a microbial food web. , 2008, Ecology letters.

[33]  S. Klamt,et al.  GSMN-TB: a web-based genome-scale network model of Mycobacterium tuberculosis metabolism , 2007, Genome Biology.

[34]  G. Macfarlane,et al.  Validation of a Three-Stage Compound Continuous Culture System for Investigating the Effect of Retention Time on the Ecology and Metabolism of Bacteria in the Human Colon , 1998, Microbial Ecology.

[35]  Pamela A. Silver,et al.  Systems engineering without an engineer: Why we need systems biology , 2007, Complex..

[36]  Pei Yee Ho,et al.  Multiple High-Throughput Analyses Monitor the Response of E. coli to Perturbations , 2007, Science.

[37]  Mikko Arvas,et al.  Common features and interesting differences in transcriptional responses to secretion stress in the fungi Trichoderma reesei and Saccharomyces cerevisiae , 2006, BMC Genomics.

[38]  A. Kierzek,et al.  Selection of objective function in genome scale flux balance analysis for process feed development in antibiotic production. , 2008, Metabolic engineering.

[39]  G. Pinto,et al.  Fatty Acids Released by Chlorella vulgaris and Their Role in Interference with Pseudokirchneriella subcapitata: Experiments and Modelling , 2010, Journal of Chemical Ecology.

[40]  C. Codeço,et al.  Competition along a Spatial Gradient of Resource Supply: A Microbial Experimental Model , 2001, The American Naturalist.

[41]  J. Hospodka CHAPTER 6 – Industrial Application of Continuous Fermentation , 1966 .

[42]  Bas Teusink,et al.  Analysis of Growth of Lactobacillus plantarum WCFS1 on a Complex Medium Using a Genome-scale Metabolic Model* , 2006, Journal of Biological Chemistry.

[43]  David Botstein,et al.  The Repertoire and Dynamics of Evolutionary Adaptations to Controlled Nutrient-Limited Environments in Yeast , 2008, PLoS genetics.

[44]  H. Westerhoff,et al.  How Geobacteraceae may dominate subsurface biodegradation: physiology of Geobacter metallireducens in slow-growth habitat-simulating retentostats. , 2009, Environmental microbiology.

[45]  A. Bull,et al.  The physiology of lactate production by Lactobacillus delbreuckii in a chemostat with cell recycle , 1989, Biotechnology and bioengineering.

[46]  Patrick H. Bradley,et al.  Growth-limiting Intracellular Metabolites in Yeast Growing under Diverse Nutrient Limitations , 2010, Molecular biology of the cell.

[47]  U. Sauer,et al.  Cyclic AMP-Dependent Catabolite Repression Is the Dominant Control Mechanism of Metabolic Fluxes under Glucose Limitation in Escherichia coli , 2008, Journal of bacteriology.

[48]  T. Ferenci 'Growth of bacterial cultures' 50 years on: towards an uncertainty principle instead of constants in bacterial growth kinetics. , 1999, Research in microbiology.

[49]  J. Grover,et al.  Coexistence of mixotrophs, autotrophs, and heterotrophs in planktonic microbial communities. , 2010, Journal of theoretical biology.

[50]  J. Snoep,et al.  Control of specific growth rate in Saccharomyces cerevisiae. , 2009, Microbiology.

[51]  J. Huisman,et al.  Principles of the light-limited chemostat: theory and ecological applications , 2002, Antonie van Leeuwenhoek.

[52]  Growth limiting substrate affects antibiotic production and associated metabolic fluxes in Streptomyces clavuligerus , 2000, Biotechnology Letters.

[53]  W. Mooij,et al.  Algal defenses, population stability, and the risk of herbivore extinctions: a chemostat model and experiment , 2009, Ecological Research.

[54]  A. Kierzek,et al.  The use of genome scale metabolic flux variability analysis for process feed formulation based on an investigation of the effects of the zwf mutation on antibiotic production in Streptomyces coelicolor , 2006 .

[55]  A. G. McKendrick,et al.  XLV.—The Rate of Multiplication of Micro-organisms: A Mathematical Study , 1912 .

[56]  S. R. L. Smith,et al.  Single cell protein , 1980 .

[57]  J. Pronk,et al.  Physiological and Transcriptional Responses of Saccharomyces cerevisiae to Zinc Limitation in Chemostat Cultures † , 2007 .

[58]  N. Panikov Microbial Growth Dynamics , 2019, Comprehensive Biotechnology.

[59]  A. Bull,et al.  Vancomycin production is enhanced in chemostat culture with biomass-recycle. , 1999, Biotechnology and bioengineering.

[60]  R. Holt,et al.  Phytoplankton species richness scales consistently from laboratory microcosms to the world's oceans. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[61]  J W Wimpenny,et al.  The gradostat: a bidirectional compound chemostat and its application in microbiological research. , 1981, Journal of general microbiology.

[62]  Jason G. Bragg,et al.  Protein carbon content evolves in response to carbon availability and may influence the fate of duplicated genes , 2007, Proceedings of the Royal Society B: Biological Sciences.

[63]  M. R. Droop,et al.  Vitamin B12 and marine ecology , 1970, Helgoländer wissenschaftliche Meeresuntersuchungen.

[64]  Grigoriy E. Pinchuk,et al.  The influence of cultivation methods on Shewanella oneidensis physiology and proteome expression , 2007, Archives of Microbiology.

[65]  B. Zomer,et al.  Modeling Neisseria meningitidis B metabolism at different specific growth rates , 2008, Biotechnology and bioengineering.

[66]  A. Tarantola Popper, Bayes and the inverse problem , 2006 .

[67]  M. Wilcox,et al.  Tigecycline does not induce proliferation or cytotoxin production by epidemic Clostridium difficile strains in a human gut model. , 2006, The Journal of antimicrobial chemotherapy.

[68]  P. Postma,et al.  Carbon flux distribution in antibiotic-producing chemostat cultures of Streptomyces lividans. , 2002, Metabolic engineering.

[69]  Lisa Chong,et al.  Whole-istic Biology , 2002, Science.

[70]  J. Heijnen,et al.  Quantitative evaluation of intracellular metabolite extraction techniques for yeast metabolomics. , 2009, Analytical chemistry.

[71]  K. Miyanaga,et al.  Spontaneous Deletion of a 209-Kilobase-Pair Fragment from the Escherichia coli Genome Occurs with Acquisition of Resistance to an Assortment of Infectious Phages , 2008, Applied and Environmental Microbiology.

[72]  J. Huisman,et al.  Competition and facilitation between unicellular nitrogen‐fixing cyanobacteria and non—nitrogen‐fixing phytoplankton species , 2007 .

[73]  Dhara Shah,et al.  Clostridium difficile infection: update on emerging antibiotic treatment options and antibiotic resistance , 2010, Expert review of anti-infective therapy.

[74]  M. Bushell,et al.  Manipulation of the physiology of clavulanic acid production in Streptomyces clavuligerus. , 1997, Microbiology.

[75]  S. J. Pirt,et al.  Principles of microbe and cell cultivation , 1975 .

[76]  N. Slakeski,et al.  Treponema denticola biofilm-induced expression of a bacteriophage, toxin-antitoxin systems and transposases. , 2010, Microbiology.

[77]  J. Pronk,et al.  Prolonged selection in aerobic, glucose-limited chemostat cultures of Saccharomyces cerevisiae causes a partial loss of glycolytic capacity. , 2005, Microbiology.

[78]  N. Torres,et al.  Analysis of the Escherichia coli response to glycerol pulse in continuous, high‐cell density culture using a multivariate approach , 2009, Biotechnology and bioengineering.

[79]  J. Grover,et al.  Dynamics and Nutritional Ecology of a Nanoflagellate Preying Upon Bacteria , 2009, Microbial Ecology.

[80]  Jacques Monod,et al.  LA TECHNIQUE DE CULTURE CONTINUE THÉORIE ET APPLICATIONS , 1978 .

[81]  B. Ollivier,et al.  Continuous enrichment cultures: insights into prokaryotic diversity and metabolic interactions in deep-sea vent chimneys , 2007, Extremophiles.

[82]  M. Simon,et al.  Significant decomposition of riverine humic-rich DOC by marine but not estuarine bacteria assessed in sequential chemostat experiments , 2008 .

[83]  T. Ferenci Bacterial physiology, regulation and mutational adaptation in a chemostat environment. , 2008, Advances in microbial physiology.

[84]  A. Novick,et al.  Experiments with the Chemostat on spontaneous mutations of bacteria. , 1950, Proceedings of the National Academy of Sciences of the United States of America.

[85]  J. Scholten,et al.  NMR bioreactor development for live in-situ microbial functional analysis. , 2008, Journal of magnetic resonance.

[86]  Alan T. Bull,et al.  Continuous Culture for Production , 1983 .

[87]  F. Srienc,et al.  Rapid strain improvement through optimized evolution in the cytostat , 2009, Biotechnology and bioengineering.

[88]  Gerardo Perozziello,et al.  Microchemostat-microbial continuous culture in a polymer-based, instrumented microbioreactor. , 2006, Lab on a chip.

[89]  P. Zilm,et al.  Co-adhesion and biofilm formation by Fusobacterium nucleatum in response to growth pH. , 2007, Anaerobe.

[90]  Juan-Rodrigo Bastidas-Oyanedel,et al.  Thermodynamic Analysis of Energy Transfer in Acidogenic Cultures , 2008 .

[91]  J. Russell The Energy Spilling Reactions of Bacteria and Other Organisms , 2007, Journal of Molecular Microbiology and Biotechnology.

[92]  M. D. Young,et al.  Enhanced product formation in continuous fermentations with microbial cell recycle * , 1981 .

[93]  G. Pinto,et al.  Allelopathy and competition between Chlorella vulgaris and Pseudokirchneriella subcapitata: Experiments and mathematical model , 2007 .

[94]  T. Ferenci A cultural divide on the use of chemostats. , 2006, Microbiology.

[95]  Pascale Daran-Lapujade,et al.  Saccharomyces cerevisiae SFP1: at the crossroads of central metabolism and ribosome biogenesis. , 2008, Microbiology.

[96]  S. Quake,et al.  Long-Term Monitoring of Bacteria Undergoing Programmed Population Control in a Microchemostat , 2005, Science.

[97]  R. Singer,et al.  Evaluating the Effects of Chlortetracycline on the Proliferation of Antibiotic-Resistant Bacteria in a Simulated River Water Ecosystem , 2007, Applied and Environmental Microbiology.

[98]  Kevin J. Flynn,et al.  Castles built on sand : dysfunctionality in plankton models and the inadequacy of dialogue between biologists and modellers , 2005 .

[99]  T. Gray,et al.  Characteristics of Arthrobacter Grown in Continuous Culture , 1974 .

[100]  The proteomic profile of Fusobacterium nucleatum is regulated by growth pH. , 2007, Microbiology.

[101]  A. Kierzek,et al.  The Genetic Requirements for Fast and Slow Growth in Mycobacteria , 2009, PloS one.

[102]  J. Pronk,et al.  Acclimation of Saccharomyces cerevisiae to low temperature: a chemostat-based transcriptome analysis. , 2007, Molecular biology of the cell.

[103]  Luke P. Lee,et al.  Microfluidics-based systems biology. , 2006, Molecular bioSystems.

[104]  J. Monod The Growth of Bacterial Cultures , 1949 .

[105]  R. Poole,et al.  Microbial responses to nitric oxide and nitrosative stress: growth, "omic," and physiological methods. , 2008, Methods in enzymology.

[106]  Zdenek Fencl,et al.  THEORETICAL AND METHODOLOGICAL BASIS OF CONTINUOUS CULTURE OF MICROORGANISMS , 1967 .

[107]  S. Brenner Sequences and consequences , 2010, Philosophical Transactions of the Royal Society B: Biological Sciences.

[108]  S. Ellner,et al.  Effects of rapid prey evolution on predator–prey cycles , 2006, Journal of mathematical biology.

[109]  W. Whitman,et al.  Functionally distinct genes regulated by hydrogen limitation and growth rate in methanogenic Archaea , 2007, Proceedings of the National Academy of Sciences.

[110]  Stephen P. Miller,et al.  Transcription, translation, and the evolution of specialists and generalists. , 2009, Molecular biology and evolution.

[111]  Yue-qin Tang,et al.  Escherichia coli Transcriptome Dynamics during the Transition from Anaerobic to Aerobic Conditions* , 2006, Journal of Biological Chemistry.

[112]  E. Franco-Lara,et al.  Proteome analysis of the Escherichia coli heat shock response under steady-state conditions , 2009, Proteome Science.

[113]  D. Ellwood,et al.  Effects of Fluoride on Carbohydrate Metabolism by Washed Cells of Streptococcus mutans Grown at Various pH Values in a Chemostat , 1978, Infection and immunity.

[114]  Bernd Blasius,et al.  Cycles, phase synchronization, and entrainment in single-species phytoplankton populations , 2010, Proceedings of the National Academy of Sciences.

[115]  D. Herbert,et al.  The continuous culture of bacteria; a theoretical and experimental study. , 1956, Journal of general microbiology.

[116]  D. Söll,et al.  Global Responses of Methanococcus maripaludis to Specific Nutrient Limitations and Growth Rate , 2008, Journal of bacteriology.

[117]  D. Minnikin,et al.  Variation of polar lipid composition of Bacillus subtilis (Marburg) with different growth conditions , 1972, FEBS letters.

[118]  F. Srienc,et al.  The cytostat: A new way to study cell physiology in a precisely defined environment. , 2006, Journal of biotechnology.

[119]  RobsonGD OliverSG TrinciAP WiebeMG Periodic selection in longterm continuous-flow cultures of the filamentous fungus Fusarium graminearum. , 1993 .

[120]  J. van den Brink,et al.  Energetic limits to metabolic flexibility: responses of Saccharomyces cerevisiae to glucose-galactose transitions. , 2009, Microbiology.

[121]  W. Cochlan,et al.  A sea‐going continuous culture system for investigating phytoplankton community response to macro‐ and micro‐nutrient manipulations , 2009 .

[122]  D. Tempest,et al.  The role of energy-spilling reactions in the growth ofKlebsiella aerogenes NCTC 418 in aerobic chemostat culture , 1976, Archives of Microbiology.

[123]  B. Bonde,et al.  Transcriptomic Analysis Identifies Growth Rate Modulation as a Component of the Adaptation of Mycobacteria to Survival inside the Macrophage , 2007, Journal of bacteriology.

[124]  Albert J R Heck,et al.  Proteome analysis of yeast response to various nutrient limitations , 2006, Molecular systems biology.

[125]  Barbara M. Bakker,et al.  Measuring enzyme activities under standardized in vivo‐like conditions for systems biology , 2010, The FEBS journal.

[126]  G. Whitesides,et al.  Microfabrication meets microbiology , 2007, Nature Reviews Microbiology.

[127]  F. Srienc,et al.  Optimized evolution in the cytostat: A Monte Carlo simulation , 2009, Biotechnology and bioengineering.

[128]  A. Bull,et al.  Enzyme evolution in a microbial community growing on the herbicide Dalapon , 1976, Nature.

[129]  Kaspar Valgepea,et al.  Specific growth rate dependent transcriptome profiling of Escherichia coli K12 MG1655 in accelerostat cultures. , 2010, Journal of biotechnology.

[130]  Bing-Zhi Li,et al.  Genome-wide transcriptional analysis of Saccharomyces cerevisiae during industrial bioethanol fermentation , 2009, Journal of Industrial Microbiology & Biotechnology.

[131]  Adilson E. Motter,et al.  Spontaneous Reaction Silencing in Metabolic Optimization , 2008, PLoS Comput. Biol..

[132]  S. Shannon,et al.  Prey Food Quality Affects Flagellate Ingestion Rates , 2006, Microbial Ecology.

[133]  Mathias Middelboe,et al.  Bacteriophages drive strain diversification in a marine Flavobacterium: implications for phage resistance and physiological properties. , 2009, Environmental microbiology.

[134]  Alex Groisman,et al.  A microfluidic chemostat for experiments with bacterial and yeast cells , 2005, Nature Methods.

[135]  S. Pirt The maintenance energy of bacteria in growing cultures , 1965, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[136]  Johannes Tramper,et al.  Modeling Neisseria meningitidis metabolism: from genome to metabolic fluxes , 2007, Genome Biology.

[137]  P. Veith,et al.  Application of 16O/18O reverse proteolytic labeling to determine the effect of biofilm culture on the cell envelope proteome of Porphyromonas gingivalis W50 , 2008, Proteomics.

[138]  Arnold L. Demain,et al.  Manual of Industrial Microbiology and Biotechnology , 1986 .

[139]  M. R. Droop,et al.  Vitamin B12 and Marine Ecology. IV. The Kinetics of Uptake, Growth and Inhibition in Monochrysis Lutheri , 1968, Journal of the Marine Biological Association of the United Kingdom.

[140]  J. Pronk,et al.  Role of Transcriptional Regulation in Controlling Fluxes in Central Carbon Metabolism of Saccharomyces cerevisiae , 2004, Journal of Biological Chemistry.

[141]  Andreas Wagner,et al.  Protein material costs: single atoms can make an evolutionary difference. , 2009, Trends in genetics : TIG.

[142]  J. Skehel,et al.  Evolution in the Microbial World , 1975 .

[143]  Anna Eliasson Lantz,et al.  Systems Biology of Antibiotic Production by Microorganisms , 2008 .

[144]  Jason Hinds,et al.  Comparative transcriptomics reveals key gene expression differences between the human and bovine pathogens of the Mycobacterium tuberculosis complex. , 2007, Microbiology.

[145]  I. Barr,et al.  Response of Porphyromonas gingivalis to Heme Limitation in Continuous Culture , 2008, Journal of bacteriology.

[146]  D. Botstein,et al.  Systematic changes in gene expression patterns following adaptive evolution in yeast. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[147]  D. Prieur,et al.  Thermodesulfatator atlanticus sp. nov., a thermophilic, chemolithoautotrophic, sulfate-reducing bacterium isolated from a Mid-Atlantic Ridge hydrothermal vent. , 2010, International journal of systematic and evolutionary microbiology.

[148]  G. Macfarlane,et al.  Acquisition, Evolution and Maintenance of the Normal Gut Microbiota , 2010, Digestive Diseases.

[149]  Alan T. Bull,et al.  The Principles of biotechnology : scientific fundamentals , 1985 .

[150]  C. Seers,et al.  Comparative transcriptomic analysis of Porphyromonas gingivalis biofilm and planktonic cells , 2009, BMC Microbiology.

[151]  S. Pirt,et al.  An extension of the theory of the chemostat with feedback of organisms. Its experimental realization with a yeast culture. , 1970, Journal of general microbiology.

[152]  J. Heijnen,et al.  Cytosolic NADPH metabolism in penicillin-G producing and non-producing chemostat cultures of Penicillium chrysogenum. , 2007, Metabolic engineering.

[153]  Matthew J. Brauer,et al.  Coordination of growth rate, cell cycle, stress response, and metabolic activity in yeast. , 2008, Molecular biology of the cell.

[154]  D. Ellwood,et al.  Continuous Culture 8: Biotechnology, Medicine and the Environment , 1984 .

[155]  A. Khodursky,et al.  Evolutionary genomics of ecological specialization. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[156]  Colin J Ingham,et al.  The micro-Petri dish, a million-well growth chip for the culture and high-throughput screening of microorganisms , 2007, Proceedings of the National Academy of Sciences.

[157]  S. Gygi,et al.  Transcriptional and Proteomic Profiles of Group B Streptococcus Type V Reveal Potential Adherence Proteins Associated with High-Level Invasion , 2007, Infection and Immunity.

[158]  Alan T. Bull,et al.  Microbial Interactions and Communities , 1982 .

[159]  Mark Dopson,et al.  Sulfate reduction at pH 5 in a high-rate membrane bioreactor: reactor performance and microbial community analyses. , 2009, Journal of microbiology and biotechnology.

[160]  H. Westerhoff,et al.  Super life – how and why ‘cell selection’ leads to the fastest‐growing eukaryote , 2009, The FEBS journal.

[161]  S. Oliver,et al.  Isolation of ethanol-tolerant mutants of yeast by continuous selection , 1982, European journal of applied microbiology and biotechnology.

[162]  A. Hollaender,et al.  Basic Biology of New Developments in Biotechnology , 1983, Basic Life Sciences.

[163]  Nathalie Q Balaban,et al.  The Moore's Law of microbiology - towards bacterial culture miniaturization with the micro-Petri chip. , 2008, Trends in biotechnology.

[164]  A. Trinci The 1994 Marjory Stephenson Prize Lecture. Evolution of the Quorn myco-protein fungus, Fusarium graminearum A3/5. , 1994, Microbiology.

[165]  Franz J Weissing,et al.  University of Groningen Nonequilibrium coexistence in a competition model with nutrient storage , 2008 .

[166]  Omar E. Cornejo,et al.  Oscillations in continuous culture populations of Streptococcus pneumoniae: population dynamics and the evolution of clonal suicide , 2008, Proceedings of the Royal Society B: Biological Sciences.

[167]  T. Ferenci,et al.  Genotype-by-Environment Interactions Influencing the Emergence of rpoS Mutations in Escherichia coli Populations , 2006, Genetics.

[168]  J. Pronk,et al.  The Penicillium chrysogenum aclA gene encodes a broad-substrate-specificity acyl-coenzyme A ligase involved in activation of adipic acid, a side-chain precursor for cephem antibiotics. , 2010, Fungal genetics and biology : FG & B.

[169]  H. E. Kubitschek Introduction to research with continuous cultures , 1970 .

[170]  J. Pronk,et al.  Quantitative Physiology of Saccharomyces cerevisiae at Near-Zero Specific Growth Rates , 2009, Applied and Environmental Microbiology.

[171]  S. Oliver,et al.  Exometabolic and transcriptional response in relation to phenotype and gene copy number in respiration‐related deletion mutants of S. cerevisiae , 2008, Yeast.

[172]  J. Heijnen,et al.  Dynamic 13C-tracer study of storage carbohydrate pools in aerobic glucose-limited Saccharomyces cerevisiae confirms a rapid steady-state turnover and fast mobilization during a modest stepup in the glucose uptake rate. , 2009, FEMS yeast research.

[173]  T. Ferenci,et al.  Clonal Adaptive Radiation in a Constant Environment , 2006, Science.

[174]  J. Nielsen,et al.  Physiology of Aspergillus niger in oxygen‐limited continuous cultures: Influence of aeration, carbon source concentration and dilution rate , 2009, Biotechnology and bioengineering.

[175]  N. Casali,et al.  Hypervirulent mutant of Mycobacterium tuberculosis resulting from disruption of the mce1 operon , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[176]  J. Pronk,et al.  Identity of the Growth-Limiting Nutrient Strongly Affects Storage Carbohydrate Accumulation in Anaerobic Chemostat Cultures of Saccharomyces cerevisiae , 2009, Applied and Environmental Microbiology.

[177]  D. C. Cooper,et al.  Responses of continuous-series estuarine microecosystems to point-source input variations. , 1973 .

[178]  Meike T. Wortel,et al.  The Timescale of Phenotypic Plasticity and Its Impact on Competition in Fluctuating Environments , 2008, The American Naturalist.

[179]  Alan T. Bull,et al.  Generation of environmentally enhanced products: Clean technology for paper chemicals , 1997 .

[180]  C. Dye,et al.  The Population Dynamics and Control of Tuberculosis , 2010, Science.