Biology of the prokaryotes: 150 tables
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Format: | Buch |
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Sprache: | German |
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Stuttgart [u.a.]
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1999
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Online-Zugang: | Inhaltsverzeichnis |
Beschreibung: | Literaturangaben |
Beschreibung: | XXVII, 955 S. zahlr. Ill., graph. Darst. |
ISBN: | 3131084111 0632053577 9780632053575 |
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adam_text | BIOLOGY OF THE PROKARYOTES EDITED BY JOSEPH W. LENGELER GERHART DREWS
HANS G. SCHLEGEL UNIVERSITY OF OSNABRUCK UNIVERSITY OF FREIBURG/BR.
UNIVERSITY OF GOTTINGEN 940 ILLUSTRATIONS 150 TABLES B THIEME STUTTGART
BLACKWELL NEW YORK 1999 SCIENCE XI CONTENTS BACTERIOLOGY PAVED THE WAY
TO CELL BIOLOGY: A HISTORICAL ACCOUNT H.G. SCHLEGEL, W. KOHLER 1.1 NEW
CONCEPTS AND EXPERIMENTAL APPROACHES PAVED THE WAY FOR PROGRESS 1 1.2
OBSERVATIONS AND SPECULATION LEAD TO THE FIRST CONCEPT OF THE EXISTENCE
OF LIVING INFECTIOUS AGENTS 2 1.3 BACTERIA ARE MEMBERS OF A NEW, LARGE
GROUP OF INDEPENDENT ORGANISMS 3 1.4 THE INTRODUCTION OF SOLID, DEFINED
MEDIA AND PURE-CULTURE METHODS MARKS A TRUE REVOLUTION 4 1.5 THE NEW
BACTERIOLOGICAL METHODS PROVED THAT THE CAUSATIVE AGENTS OF INFECTIOUS
DISEASES ARE BACTERIA 5 1.6 STUDIES ON FERMENTATION FOUNDED BACTERIAL
PHYSIOLOGY AND BIOCHEMISTRY 6 1.7 LITHOAUTOTROPHY IS THE ABILITY OF
BACTERIA TO OBTAIN ENERGY FROM THE OXIDATION OF INORGANIC COMPOUNDS AND
CARBON FROM CARBON DIOXIDE 6 1.8 LIGHT-DEPENDENT PROCESSES SUCH AS
PHOTOTAXIS, LIGHT-INDUCED ENERGY TRANSDUCTION, AND THE PHOTOASSIMILATION
OF CARBON DIOXIDE TOOK A LONG TIME TO BE UNDERSTOOD 7 1.9 DINITROGEN
FIXATION IS UNIQUE TO THE PROKARYOTES 8 1.10 THE ANALYSIS OF ANABOLIC
AND CATABOLIC METABOLISM LEAD TO THE DISCOVERY OF SUBSTRATES, PRODUCTS,
APOENZYMES, AND COENZYMES, AND, IN THE END, OF METABOLIC PATHWAYS 9 1.11
STUDIES ON INCLUSION BODIES AND THE STRUCTURES AND FUNCTIONS OF CELL
ENVELOPES REVEALED THE ORGANIZATION OF THE BACTERIAL CELL 10 1.12
BACTERIAL ADAPTATION WAS WELL RECOGNIZED BEFORE THE GENETIC APPROACH
REVEALED THE BASIS OF MOLECULAR MECHANISMS OF REGULATION C . 11 1.13
STUDIES ON THE METABOLIC TYPES OF BACTERIA REVEALED THEIR FUNCTIONS IN
THE BIOSPHERE 12 1.14 THE GOALS AND METHODS OF THE CLASSIFICATION OF
BACTERIA HAVE CHANGED 13 1.15 BACTERIAL VIRUSES (BACTERIOPHAGES) WERE
DETECTED AS LYTIC PRINCIPLES 13 1.16 STUDIES ON HEREDITY IN BACTERIA
PROVIDES THE DECISIVE PRINCIPLES AND CONCEPTS FOR THE PROMOTION OF
MODERN BIOLOGY INCLUDING GENE TECHNOLOGY 14 1.17 EPILOGUE . 15 SECTION I
THE PROKARYOTIC CELL F. MAYER 2 2.1 2.2 CELLULAR AND SUBCELLULAR
ORGANIZATION OF PROKARYOTES. F. MAYER 20 PROKARYOTES, THOUGH SMALL,
CONTAIN ALL STRUCTURAL ELEMENTS NECESSARY FOR SURVIVAL AND
MULTIPLICATION 20 CELLULAR STRUCTURES CAN BE MADE VISIBLE OR IDENTIFIED
BY NUMEROUS METHODS 22 2.3 PROKARYOTES MAY OCCUR AS SINGLE CELLS OR AS
CELL ASSOCIATIONS 25 2.4 THE STRUCTURAL COMPONENTS OF PROKARYOTIC CELL
ENVELOPES ARE ORGANIZED AS BARRIERS AND INTERFACES 27 XII CONTENTS 2.5
THE SETUP OF THE INTRACELLULAR STRUCTURES REFLECTS THE HIGH DEGREE OF
ORGANIZATION IN THE PROKARYOTIC CELL 36 2.6 CELL APPENDAGES SERVE FOR
LOCOMOTION AND CELL RECOGNITION 41 2.7 BACTERIA MAY FORM SPORES AND
OTHER RESTING CELLS 44 SECTION II BASIC PREREQUISITES FOR CELLULAR LIFE
A. KROGER, C. FUCHS 3 SUBSTRATE-LEVEL PHOSPHORYLATION A. KROGER 3.1 ATP
SYNTHESIS IS COUPLED TO EXERGONIC REACTIONS 48 3.2 THE ATP YIELD IS A
FUNCTION OF THE FREE ENERGY OF THE DRIVING REACTION 49 3.3 COUPLING OF
ATP SYNTHESIS TO GLUCOSE DEGRADATION REQUIRES C-C CLEAVAGE AND
SUBSEQUENT OXIDATION 51 48 3.4 A HIGH-ENERGY COMPOUND IS FORMED IN SLP
52 3.5 PYRUVATE OXIDATION IS COUPLED TO ENERGY CONSERVATION 55 3.6 THE
CATABOLIC FUNCTION OF THE CITRATE CYCLE IS TO PROVIDE REDUCING
EQUIVALENTS FOR OXIDATIVE PHOSPHORYLATION 55 4
ELECTRON-TRANSPORT-COUPLED PHOSPHORYLATION A. KROGER 4.1 IN ETP, THE
AMOUNT OF ATP FORMED 4.4 CORRESPONDS WITH THE FREE ENERGY OF THE *
DRIVING REDOX REACTION 7 59 4.2 ALL ATP SYNTHASES OPERATE ACCORDING TO
THE 4.5 SAME MECHANISM 62 4.3 THERE ARE MANY DIFFERENT RESPIRATORY
CHAINS 63 59 THERE ARE MANY DIFFERENT MECHANISMS OF COUPLING ELECTRON
TRANSPORT TO PROTON TRANSPORT 65 IN PHOTOPHOSPHORYLATION, ELECTRON
TRANSPORT AND PROTON TRANSLOCATION ARE DRIVEN BY LIGHT 67 5 MULTIPLE
ROLES OF PROKARYOTIC CELL MEMBRANES R. KRAMER 5.1 BACTERIAL MEMBRANES
FUNCTION AS 5.5 PERMEABILITY BARRIERS 68 5.2 THE STRUCTURE AND FUNCTION
OF TRANSPORT IS 5.6 DICTATED BY THE MEMBRANE 69 5.3 FORMAL CONCEPTS OF
TRANSPORTER FUNCTION... 70 5.7 5.4 STUDYING KINETICS OF TRANSPORT IS
USEFUL FOR IDENTIFICATION AND CHARACTERIZATION OF 5.8 TRANSPORT
PROCESSES 72 68 ENERGETICS OF CARRIER-MEDIATED TRANSPORT: THE CONCEPT OF
COUPLING 73 THERE ARE MANY DIFFERENT TRANSPORT MECHANISMS IN PROKARYOTES
74 REGULATION AND DIVERSITY OF TRANSPORT SYSTEMS 84 SECRETION OF
MACROMOLECULES 86 6 GROWTH AND NUTRITION C. FUCHS, A. KROGER 6.1 GROWTH
CHARACTERISTICS OF A BATCH CULTURE IS A REFLECTION OF CELL PHYSIOLOGY 88
6.2 PHYSICOCHEMICAL FACTORS AFFECT GROWTH AND MORE 90 88 6.3 GROWTH
MEDIA PROVIDE ALL ESSENTIAL NUTRIENTS 95 6.4 STERILIZATION OF MEDIA AND
EQUIPMENT ARE A MUST FOR MAINTAINING PURE CULTURES 99 CONTENTS XIII 6.5
GROWTH CAN BE MEASURED BY VARIOUS METHODS 100 6.6 CULTURE PRESERVATION
MAINTAINS BACTERIA ALIVE FOR A LONG TIME 102 6.7 SELECTIVE CULTURE
METHODS, ENRICHMENT, AND ISOLATION ARE PERMANENT TASKS OF
MICROBIOLOGISTS 102 6.8 CONTINUOUS CULTURES ARE VALUABLE TOOLS 103 6.9
PRESERVATION METHODS ARE BASED ON THE INHIBITION OF MICROBIAL GROWTH 108
7 BIOSYNTHESIS OF BUILDING BLOCKS G. FUCHS 7.1 THE MOLECULAR COMPOSITION
REFLECTS THE COMPLEXITY OF THE PROKARYOTIC CELL ILL 7.2 THE FEW CENTRAL
PRECURSOR METABOLITES ARE INTERMEDIATES OF THE CENTRAL METABOLIC
PATHWAYS 114 7.3 HOW NITROGEN, PHOSPHORUS, SULFUR, ONE- CARBON UNITS,
AND MOLECULAR OXYGEN ARE INCORPORATED INTO CELL COMPOUNDS 116 7.4 THE
FORMATION OF BUILDING BLOCKS FROM CENTRAL PRECURSOR METABOLITES,
POLYMERIZATION, AND THE FINAL ASSEMBLY OF MACROMOLECULES COST ATP AND
NADPH 123 7.5 CENTRAL BIOSYNTHETIC PRECURSOR METABOLITES FROM WHICH THE
CELLULAR BUILDING BLOCKS ARE FORMED DERIVE FROM THREE MAIN METABOLIC
PATHWAYS 125 110 7.6 AMINO ACIDS DERIVE FROM FEW CENTRAL PRECURSOR
METABOLITES 127 7.7 CARBOHYDRATE PHOSPHATES ARE IMPORTANT PRECURSORS OF
MANY BUILDING BLOCKS 135 7.8 THE BUILDING BLOCKS OF NUCLEIC ACIDS ARE
RIBONUCLEOTIDES AND DEOXYRIBONUCLEOTIDES .. 138 7.9 SUGARS AND SUGAR
NUCLEOTIDES ARE IMPORTANT BUILDING BLOCKS 143 7.10 THE BIOSYNTHESIS OF
LIPIDS IS AS COMPLEX AS THEIR STRUCTURE 147 7.11 ALL BACTERIA SYNTHESIZE
ONE OR MORE POLYMERIC STORAGE COMPOUNDS 155 7.12 MANY SOLUBLE COMPOUNDS
ARE ESSENTIAL AND ONLY REQUIRED IN SMALL AMOUNTS 157 SECTION III
DIVERSITY OF METABOLIC PATHWAYS C. FUCHS ASSIMILATION OF MACROELEMENTS
AND MICROELEMENTS. G. FUCHS 163 8.1 AUTOTROPHIC BACTERIA USE CO 2 AS
SOLE SOURCE OF CARBON 163 8.2 GENERATION OF PRECURSOR METABOLITES FROM C
2 COMPOUNDS AS CARBON SOURCE REQUIRES SPECIFIC REACTIONS 173 8.3
METHYLOTROPHIC BACTERIA USE C, COMPOUNDS AS THE ONLY CARBON SOURCE 174
8.4 AMMONIA CAN BE OBTAINED JROM VARIOUS NITROGEN SOURCES 176 8.5
REDUCTION OF N 2 TO NH 3 IS CATALYZED BY NITROGENASE 177 8.6
ASSIMILATION OF PHOSPHORUS DOES NOT REQUIRE REDOX REACTIONS 181 8.7
COMMON SOURCES OF CELL SULFUR ARE SULFATE AND THIOSULFATE 181 8.8 TRACE
ELEMENTS AND ELECTROLYTES ARE TAKEN UP BY SPECIFIC TRANSPORT SYSTEMS 182
9 OXIDATION OF ORGANIC COMPOUNDS C. FUCHS 9.1 UTILIZATION OF POLYMERIC
ORGANIC SUBSTRATES DEPENDS ON EXTRACELLULAR STEPS OF DEGRADATION 189 9.2
EXTRACELLULAR ENZYMES ARE EXPORTED INTO THE SURROUNDING MEDIUM OR TO THE
CELL SURFACE 189 9.3 FORMATION AND SECRETION OF EXTRACELLULAR ENZYMES
ARE REGULATED 190 187 9.4 INTRACELLULAR STORAGE POLYMERS ARE DEGRADED BY
CELLULAR ENZYMES 191 9.5 DEGRADATION OF MAJOR POLYMERIC SUBSTRATES INTO
SOLUBLE PRODUCTS IS CATALYZED BY EXOENZYMES 192 9.6 LIGNIN IS A
HETEROPOLYMER OF PHENYLPROPANE UNITS 198 CONTENTS 9.7 PROTEIN IS A
SUBSTRATE FOR MANY MICROORGANISMS 201 9.8 RIBONUCLEIC AND
DEOXYRIBONUCLEIC ACIDS . ARE UBIQUITOUS BIOPOLYMERS THAT ARE EASILY
DEGRADED BY EXTRACELLULAR HYDROLASES 202 9.9 LIPIDS ARE MEMBRANE
CONSTITUENTS OF ALL ORGANISMS 203 9.10 THERE ARE VARIANTS OF THE CENTRAL
PATHWAYS INTO WHICH PRODUCTS OF BIOPOLYMER DEGRADATION ARE CHANNELED 204
9.11 SEVERAL PATHWAYS SERVE FOR THE OXIDATION OF CARBOHYDRATES, THE MOST
COMMON SUBSTRATES 205 9.12 AMINO ACIDS ARE THE SECOND MOST COMMON
SUBSTRATES 212 9.13 AEROBIC DEGRADATION OF AROMATIC COMPOUNDS REQUIRES
MOLECULAR OXYGEN; ANAEROBIC PATHWAYS ARE QUITE DIFFERENT 215 9.14 FATTY
ACIDS, WAXES, HYROCARBONS, STEROLS, AND CT COMPOUNDS CAN BE USED BY
SPECIALISTS 222 9.15 THE NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS ARE
A LARGE AND HETEROGENEOUS GROUP OF BIOLOGICALLY IMPORTANT SUBSTANCES.
227 9.16 ORGANIC ACIDS ARE COMMON NATURAL SUBSTRATES THAT ARE ALSO
FORMED SECONDARILY BY FERMENTATIONS 229 9.17 XENOBIOTIC COMPOUNDS ARE
MAN-MADE RECALCITRANT POLLUTANTS THAT NORMALLY DO NOT OCCUR IN NATURE
230 9.18 SOME BACTERIA OXIDIZE SIMPLE ORGANIC COMPOUNDS INCOMPLETELY 232
10 10.1 10.2 10.3 10.4 10.5 OXIDATION OF INORGANIC COMPOUNDS BY
CHEMOLITHOTROPHS 234 G. KUENEN CHEMOLITHOTROPHS DERIVE ENERGY FROM THE
OXIDATION OF INORGANIC COMPOUNDS 234 THERE ARE NUMEROUS METABOLIC TYPES
AMONG THE CHEMOLITHOTROPHS 238 MECHANISMS OF ENERGY CONSERVATION IN
CHEMOLITHOTROPHS ARE PRINCIPALLY THE SAME AS IN CHEMOHETEROTROPHS 239
THE CARBON METABOLISM OF CHEMOLITHOTROPHS IS NOT DIFFERENT FROM THAT OF
HETEROTROPHS AND PHOTOTROPHS 241 CHEMOLITHOTROPHS ARE ADAPTED TO
SPECIFIC AND VERY OFTEN EXTREME ENVIRONMENTS DEFICIENT IN ORGANIC MATTER
243 10.6 THE SULFUR-OXIDIZING BACTERIA ARE A HETEROGENEOUS GROUP 245
10.7 THE NITRIFYING BACTERIA OXIDIZE AMMONIUM AND NITRITE 251 10.8 THE
KNALLGAS BACTERIA GAIN ENERGY FROM HYDROGEN OXIDATION 254 10.9 THE
CARBON MONOXIDE-OXIDIZING BACTERIA ARE FACULTATIVE CHEMOLITHOAUTOTROPHS
256 10.10 THE IRON- AND MANGANESE-OXIDIZING BACTERIA 257 11 11.1 11.2
11.3 11.4 AEROBIC RESPIRATION AND REGULATION OF AEROBIC/ANAEROBIC
METABOLISM 261 G. UNDER) PROPERTIES OF MOLECULAR OXYGEN 261 OXYGEN
FULFILLS DIVERSE FUNCTIONS IN METABOLISM 263 OXYGEN MAKES HIGH ENERGY
YIELDS POSSIBLE. 267 O 2 CAN SERVE AS A CO-SUBSTRATE FOR METABOLISM 274
11.5 BACTERIA RESPOND TO THE EFFECT OF TOXIC OXYGEN SPECIES 275 11.6
BIOLUMINESCENT SYSTEMS REQUIRE OXYGEN FOR LIGHT EMISSION 276 12
ANAEROBIC ENERGY METABOLISM W. BUCKET 12.1 ANAEROBIC ELECTRON TRANSPORT
PHOSPHORYLATION USES ELECTRON ACCEPTORS OTHER THAN OXYGEN 278 278 12.2
FERMENTATION IS AN ANAEROBIC REDOX PROCESS 296 12.3 ENERGY CAN BE
CONSERVED BY NON-REDOX REACTIONS 324 CONTENTS XV 13 UTILIZATION OF LIGHT
BY PROKARYOTES , G. DREWS 13.1 THREE GROUPS OF PIGMENTS ARE ACTIVE IN
PHOTOSYNTHESIS 328 13.2 THE PHOTOSYNTHESIS OF GREEN BACTERIA, PURPLE
BACTERIA, AND HELIOBACTERIA IS ANOXYGENIC 330 13.3 THE PHOTOSYNTHESIS OF
CYANOBACTERIA IS OXYGENIC 336 327 13.4 BACTERIORHODOPSIN I IS A
LIGHT-DRIVEN PROTON PUMP OF HALOBACTERIUM HALOBIUM 338 13.5
SPECTROSCOPICAL, BIOCHEMICAL, AND GENETIC METHODS ARE USED TO STUDY
BACTERIAL PHOTOSYNTHESIS 340 SECTION IV THE GENETICS OF THE PROKARYOTES
AND THEIR VIRUSES 6. FRIEDRICH, ].W. LENGELER 14 DNA, CHROMOSOMES, AND
PLASMIDS IV. MESSER 14.1 DNA IS THE CARRIER OF GENETIC INFORMATION IN
BACTERIA 343 14.2 MOST BACTERIA HAVE ONE CIRCULAR CHROMOSOME 353 343
14.3 PLASMIDS ARE INDEPENDENT REPLICONS 354 14.4 TRANSPOSONS ARE MOBILE
GENETIC ELEMENTS .. 357 15 15.1 15.2 15.3 16 16.1 16.2 16.3 THE GENETIC
INFORMATION W. HILLEN THE ORGANIZATION OF THE GENETIC MATERIAL IN
BACTERIA _... 364 TRANSCRIPTION: THE SYNTHESIS OF AN RNA COMPLEMENTARY
TO THE CODOGENIC DNA STRAND 365 TRANSLATION IS THE SYNTHESIS OF PROTEINS
DIRECTED BY RNA TEMPLATES 369 362 15.4 THE GENETIC CODE IS A DEGENERATE
AND UNIVERSAL TRIPLET CODE 374 15.5 MUTATIONS AND MUTANT SELECTION IN
BACTERIA ARE ESSENTIAL GENETIC METHODS 376 15.6 THE STABILITY OF THE
BACTERIAL GENOME IS INCREASED BY DNA REPAIR 381 15.7 THE SOS RESPONSE IN
. COFI IS INDUCED BY SINGLE-STRANDED DNA 384 GENETIC EXCHANGE BETWEEN
MICROORGANISMS. LANKA, W. PANSEGRAU UPTAKE OF FREE DNA CAN RESULT IN
GENETIC 16.4 TRANSFORMATION OF BACTERIA 386 CONJUGATIVE DNA TRANSFER
REQUIRES INTIMATE CELL-CELL CONTACT 389 16.5 TRANSDUCTION IS MEDIATED BY
BACTERIOPHAGES CARRYING NON-VIRAL GENETIC INFORMATION 406 386 HOMOLOGOUS
RECOMBINATION IS AN IMPORTANT PATHWAY FOR GENOMIC INCORPORATION OF
EXOGENOUS DNA 408 DNA RESTRICTION AND MODIFICATION PROTECTS THE CELL
AGAINST FOREIGN DNA 413 17 RECOMBINANT DNA TECHNOLOGY , R. KNIPPERS,
C.-A. ALPERT 17.1 GENOMIC LIBRARIES CONTAIN DEFINED DNA FRAGMENTS 416
17.2 GENOMIC (DNA) LIBRARIES ARE OFTEN USED AS STARTING POINTS FOR THE
ANALYSIS OF GENES AND THEIR PRODUCTS 425 416 17.3 DNA SEQUENCING IS AN
IMPORTANT TECHNIQUE IN BIOLOGICAL RESEARCH 426 17.4 LOCALIZED
MUTAGENESIS HELPS TO IDENTIFY SPECIFIC FUNCTIONS 428 XVU CONTENTS
SECTION V GENE EXPRESSION AND REGULATORY MECHANISMS J.W. LENGELER 18
REGULATION OF GENE EXPRESSION: OPERONS AND REGULONS. S. ADHYA 437 18.1
OPERONS AND REGULONS ARE UNITS OF TRANSCRIPTION 437 18.2 A REGULATOR
OFTEN CONTROLS ITS OWN SYNTHESIS: AUTOREGULATION 441 18.3 THE BACTERIAL
RNA POLYMERASE IS A MULTISUBUNIT ENZYME THAT INITIATES TRANSCRIPTION AT
THE PROMOTER 441 18.4 NEGATIVE CONTROL DECREASES TRANSCRIPTION... 442
18.5 POSITIVE CONTROL ACTIVATES TRANSCRIPTION 444 18.6 REGULATORY
PROTEINS OFTEN HAVE A DUAL ROLE 448 18.7 MIXED CONTROL: REPRESSOR
INHIBITS ACTIVATOR 449 18.8 DNA STRUCTURE ALSO REGULATES TRANSCRIPTION
INITIATION 450 18.9 REGULATION OCCURS BY ALTERING RNA POLYMERASE
STRUCTURE AND FUNCTION 451 18.10 TRANSCRIPTION, ELONGATION AND
TERMINATION ARE ALSO REGULATED 452 18.11 GENES CAN ALSO BE TURNED ON AND
OFF BY DNA RECOMBINATION 457 18.12 GENE EXPRESSION IS REGULATED BY RNA
METABOLISM 458 18.13 TRANSLATION IS OFTEN REGULATED 459 18.14
PROTEOLYSIS CAN DETERMINE LEVELS OF GENE PRODUCTS 464 18.15 DNA-PROTEIN
INTERACTIONS PLAY KEY ROLES IN GENE REGULATION 464 18.16 SUMMARY 467 19
19.1 19.2 19.3 POSTTRANSLATIONAL CONTROL AND MODIFICATIONS OF PROTEINS.
G.R. JACOBSON 469 POSTTRANSLATIONAL CONTROL ALLOWS BACTERIA TO ADAPT
RAPIDLY 469 ALLOSTERIC CONTROL OF ENZYME ACTIVITY IS WIDESPREAD AMONG
PROKARYOTES 470 POSTTRANSLATIONAL COVALENT MODIFICATIONS OF PROTEINS
CONTROL A WIDE VARIETY OF PROCESSES IN THE PROKARYOTES 476 19.4
POSTTRANSLATIONAL CONTROL INCLUDES ENZYMES AND PROTEIN
COMPARTMENTALIZATION WITHIN THE UNICELLULAR PROKARYOTES 484 20 20.1 20.2
20.3 GLOBAL REGULATORY NETWORKS AND SIGNAL TRANSDUCTION PATHWAYS J.W.
LENGELER, P.W. POSTMA 491 PROKARYOTES CONTAIN INTEGRATED METABOLIC
NETWORKS AND SIGNAL TRANSDUCTION PATHWAYS 491 CARBON CATABOLITE
REPRESSION IS INTIMATELY LINKED TO OTHER PHENOMENA 499 THE RELA/SPOT
MODULON CONTROLS ANABOLIC PATHWAYS AND MACROMOLECULE BIOSYNTHESIS 505
20.4 SIGNAL TRANSDUCTION VIA TWO-COMPONENT REGULATORY SYSTEMS IS LINKED
TO GLOBAL REGULATORY SYSTEMS 509 20.5 BACTERIAL CHEMOTAXIS IS ANOTHER
PARADIGM FOR SIGNAL TRANSDUCTION THROUGH A TWO- COMPONENT SYSTEM 514 21
21.1 REGULATION OF FERMENTATION AND RESPIRATION. E.C.C. LIN THERE ARE
THREE BASIC MODES OF ENERGY GENERATION 524 21.2 FERMENTATION INVOLVES
BOTH GLOBAL AND SPECIFIC REGULATION OF GENE EXPRESSION , 524 525
CONTENTS XVII 21.3 ANAEROBIC RESPIRATION AND ITS CONTROL REQUIRE A
COMPLEX REGULATORY NETWORK 529 21.4 CONTROL OF AEROBIC RESPIRATION
INVOLVES A TWO-COMPONENT SYSTEM 532 21.5 AEROBIC METABOLISM IS
ASSOCIATED WITH FORMATION OF HARMFUL OXYGEN SPECIES (OXYGEN STRESS) 535
21.6 OVERVIEW 536 SECTION VI CELL GROWTH AND DIFFERENTIATION C. DREWS,
J.W. LENGELER 22 THE BACTERIAL CELL CYCLE K. NORDSTROM 22.1 KEY EVENTS
DETERMINE THE DIFFERENT PERIODS OF THE VEGETATIVE CELL CYCLE 541 22.2
STRATEGIES OF DNA REPLICATION FOR CHROMOSOMES AND PLASMIDS 545 541 22.3
THE NUCLEOID OF PROKARYOTES IS THE EQUIVALENT OF THE NUCLEUS OF
EUKARYOTES 548 22.4 THE CELL CYCLE CONSISTS OF CONTROLLED AND
COORDINATED PROCESSES 550 22.5 CONCLUDING REMARKS 553 23 ASSEMBLY OF
CELLULAR SURFACE STRUCTURES . K. JANN, B. JANN 23.1 PEPTIDOGLYCAN, THE
RIGID LAYER OF CELL WALLS, IS ASSEMBLED FROM ACTIVATED PRECURSORS 555
23.2 LIPOPOLYSACCHARIDES, ESSENTIAL COMPONENTS OF THE GRAM-NEGATIVE CELL
WALL, ARE SYNTHESIZED FROM BUILDING BLOCKS AT THE CYTOPLASMIC MEMBRANE
557 23.3 TEICHOIC ACIDS AND LIPOTEICHOIC ACIDS ARE POLYOL-CONTAINING
CELL-WALL COMPONENTS OF GRAM-POSITIVE BACTERIA 562 23.4 TEICHURONIC
ACIDS ARE HEXURONIC-ACID- CONTAINING SURFACE COMPONENTS OF GRAM-
POSITIVE BACTERIA 563 23.5 THE CAPSULES SURROUNDING MANY GRAM- POSITIVE
AND GRAM-NEGATIVE BACTERIA AS A PROTECTIVE LAYER CONSIST OF ACIDIC
POLYSACCHARIDES 564 555 23.6 POLYSACCHARIDE ASSEMBLY IS SHUNTED TO THE
UNDECAPRENOL PHOSPHATE CYCLE 565 23.7 OUTER MEMBRANE PROTEINS OF
GRAM-NEGATIVE BACTERIA ARE EITHER PORE-FORMING PROTEINS (PORINS) OR
STRUCTURAL PROTEINS 566 23.8 THE FILAMENTOUS FIMBRIAE INTERACT WITH
RECEPTORS OF CELL SURFACES 568 23.9 THE FLAGELLA, ORGANELLES OF
MOTILITY, ARE ASSEMBLED BY TWO MECHANISMS 569 23.10 THE SURFACE AND THE
FLAGELLA OF ARCHAEBACTERIA CONSIST OF GLYCOPROTEINS 569 24 PROCESSES OF
CELLULAR DIFFERENTIATION G. DREWS 24.1 IN CAULOBACTER, THE FORMATION OF
SWARMER AND STALKED CELLS IS REGULATED BY THE CELL CYCLE 24.2 MEMBRANE
DIFFERENTIATION IN FACULTATIVELY PHOTOTROPHIC BACTERIA IS REGULATED BY
SHIFTS 571 571 OF OXYGEN TENSION AND LIGHT INTENSITY 575 24.3
HETEROCYSTS ARE CELLS IN CYANOBACTERIA SPECIALIZED FOR FIXATION OF
DINITROGEN 581 25 SPORULATION AND CELL DIFFERENTIATION MA. MARAHIEL, P.
ZUBER 25.1 SPORULATION IN BACILLUS SUBTILIS IS A MULTI-STEP PROCESS THAT
CAN BE DISSECTED GENETICALLY; THE FORMATION OF ENDOSPORES 586 586 25.2
SPORULATION IN STREPTOMYCETES PRODUCES EXOSPORES 593 25.3 MULTICELLULAR
DEVELOPMENT IN MYXOCOCCUS XANTHUS, A SOCIAL ORGANISM 598 KVIII. CONTENTS
26 26.1 26.2 26.3 BACTERIOPHAGES AS MODELS FOR DIFFERENTIATION. 6.
KEMPER 602 INTRODUCTION AND EXPERIMENTAL TECHNIQUES . 602 COMPOSITION
AND PLAQUE MORPHOLOGY ARE USED FOR CLASSIFICATION OF BACTERIOPHAGES ...
604 THE LYTIC INFECTION CYCLE IS CHARACTERISTIC FOR VIRULENT PHAGES 608
26.4 LYSOGENIC PATHWAYS, AN ALTERNATIVE LIFE FOR TEMPERATE PHAGES 616
26.5 PHAGES ARE IMPORTANT GENETIC TOOLS 623 27 27.1 27.2 27.3 SECONDARY
METABOLISM IN BACTERIA: ANTIBIOTIC PATHWAYS, REGULATION, AND FUNCTION...
C. LANCINI, A.L. DEMAIN 627 MOST SECONDARY METABOLITES ARE MADE BY A FEW
BIOSYNTHETIC PATHWAYS 627 SMALL ANTIBIOTIC MOLECULES ARE BIOSYNTHESIZED
THROUGH REACTIONS RELATED TO PRIMARY INTERMEDIARY METABOLISM 628 SEVERAL
CLASSES OF SECONDARY METABOLITES ARE DERIVED FROM POLYKETOMETHYLENE
CHAINS ... 632 27.4 TWO POLYMERIZATION MECHANISMS ARE USED FOR THE
SYNTHESIS OF POLYPEPTIDE ANTIBIOTICS. 637 27.5 AMINOGLYCOSIDE
ANTIBIOTICS PRODUCED BY ACTINOMYCETES ARE DERIVED FROM CARBOHYDRATE
OLIGOMERIZATION 639 27.6 SIMILAR TO OTHER DIFFERENTIATION PROCESSES,
SECONDARY METABOLISM IS HIGHLY REGULATED.. 644 27.7 SECONDARY
METABOLITES HAVE ESSENTIAL FUNCTIONS IN NATURE 647 28 ADAPTATION TO
EXTREME ENVIRONMENTS .. I.R. BOOTH 28.1 ADAPTATION TO STRESS REQUIRES
PHYSIOLOGICAL CHANGES AND CHANGES IN GENE EXPRESSION .. 652 28.2
ADAPTATION TO EXTREME TEMPERATURE 657 28.3 BACTERIA CAN ADAPT TO
EXTREME PH VALUES .. 660 28.4 BACTERIA ADOPT A COMMON STRATEGY FOR
SURVIVING OSMOTIC STRESS 665 652 28.5 CHANGES IN GROWTH RATE ELICIT AN
ADAPTIVE RESPONSE 668 28.6 CONCLUSION: THE STRESS RESPONSE IS AN
EXAGGERATED NORMAL RESPONSE 671 SECTION VII DIVERSITY AND SYSTEMATICS E.
STACKEBRANDT 29 PROKARYOTIC DIVERSITY AND SYSTEMATICS E. STACKEBRANDT,
B. TINDALL, W. LUDWIG, M. GOODFELLOW 29.1 BACTERIAL SYSTEMATICS IS THE
CRADLE OF 29.4 COMPARATIVE BIOLOGY 675 29.2 NUMERICAL TAXONOMY IS AN
APPROACH TO 29.5 CLUSTER STRAINS ON THE BASIS OF LARGE SETS OF 29.6
UNWEIGHTED PHENETIC DATA 680 29.3 CHEMICAL CHARACTERIZATION OF THE CELL
AS A 29.7 TAXONOMIC TOOL 684 674 GENOMIC CHARACTERIZATION OF STRAINS AND
SPECIES 695 PHYLOGENETIC TREES AND THEIR INTERPRETATION . 700 FROM EARLY
LIFE FORMS TO EXTANT SPECIES OF PROKARYOTES 705 THE POLYPHASIC APPROACH
TO BACTERIAL SYSTEMATICS 717 CONTENTS XIX SECTION VIM PROKARYOTES IN THE
BIOSPHERE B. SCHINK 30 30.1 30.2 30.3 30.4 ECOPHYSIOLOGY AND ECOLOGICAL
NICHES OF PROKARYOTES 723 6. SCHINK SUBSTRATES IN NATURE ARE TYPICALLY
LIMITING. 723 BACTERIA ARE ACTIVE IN REDOX TRANSFORMATIONS 728 GROWTH
KINETICS IN A NATURAL ECOSYSTEM 733 SUBSTRATE TURNOVER IS DETERMINED BY
DEPOLYMERIZATION AND SUBSTRATE UPTAKE KINETICS 740 30.5 MANY BACTERIA
LIVE ATTACHED TO SURFACES 746 30.6 TRANSPORT IS ACCOMPLISHED BY
CONVECTION AND DIFFUSION ALONG GRADIENTS 751 30.7 MICROORGANISMS
COOPERATE IN VARIOUS WAYS . 754 31 31.1 31.2 31.3 31.4 HABITATS OF
PROKARYOTES B. SCHINK 763 763 WATER IS A PERFECT BASIS FOR MICROBIAL
LIFE SEDIMENTS RESEMBLE DIGESTING ORGANS AND ARE HISTORY NOTEBOOKS 775
SOIL IS MOSTLY DRY AND HETEROGENEOUS 779 EXTREME ENVIRONMENTS ARE
HABITATS FOR SPECIALISTS 784 31.5 ASSOCIATIONS WITH ANIMAL DIGESTIVE
TRACTS 792 31.6 OTHER ASSOCIATIONS WITH ANIMALS 800 31.7 MICROBES AND
PLANTS 801 32 GLOBAL BIOGEOCHEMICAL CYCLES B. SCHINK 32.1 THE CARBON
CYCLE IS GOVERNED BY PHOTOSYNTHESIS R 804 32.2 PROKARYOTES CONTRIBUTE TO
ALL STEPS OF THE NITROGEN CYCLE 807 804 32.3 PROKARYOTES PARTICIPATE IN
ALL STEPS OF THE SULFUR CYCLE 808 32.4 FEW OTHER ELEMENTS UNDERGO
TRANSFORMATIONS IN CYCLES 811 SECTION IX APPLIED MICROBIOLOGY A. PUH/ER
33 PROKARYOTES IN MEDICINE J. HACKER 33.1 SIGNIFICANCE OF INFECTIOUS
DISEASES 815 33.2 HOST DEFENSE MECHANISMS 821 33.3 BACTERIAL VIRULENCE
FACTORS 825 33.4 VARIATION AND REGULATION OF GENES INVOLVED IN VIRULENCE
836 815 33.5 DIAGNOSIS, THERAPY, PROPHYLAXIS: PROBLEMS AND NEW
APPROACHES 841 33.6 PROKARYOTES IN MEDICINE: FUTURE TRENDS AND
DEVELOPMENTS 847 34 PROKARYOTES IN AGRICULTURE F. O GARA, U.B. PRIEFER,
D.N. DOWLING, M.P. NUTI 34.1 SOIL PROKARYOTES CAN BE MONITORED BY
VARIOUS METHODS 851 850 34.2 BACTERIA CAN BE USED AS BIOFERTILIZERS 853
34.3 BACTERIA CAN PROMOTE PLANT DISEASES 862 XX I CONTENTS 34.4 BACTERIA
CAN ENHANCE PLANT GROWTH AND RESISTANCE 868 34.5 BACTERIA CAN CONTRIBUTE
TO BIODEGRADATION OF POLLUTANTS IN SOIL 871 35 PROKARYOTES IN INDUSTRIAL
PRODUCTION H. SAHM 35.1 A LIMITED NUMBER OF STRAINS HAVE BEEN SELECTED
AND IMPROVED FOR INDUSTRIAL PRODUCTION 875 35.2 LARGE-SCALE CULTIVATION
OF MICROORGANISMS DEPENDS ON THE TYPE OF THE PROCESS 877 35.3 FOOD
INDUSTRY IS AN IMPORTANT BRANCH OF BIOTECHNOLOGY 879 35.4 PRODUCTION OF
L-AMINO ACIDS AND VITAMINS IS NOT A CLASSICAL FERMENTATION PROCESS 882
874 35.5 STEROIDS AND STEROLS CAN BE STEREOSPECIFICALLY BIOTRANSFORMED
INTO THE DESIRABLE HORMONES 888 35.6 ANTIBIOTICS ARE PRODUCTS OF
MICROORGANISMS THAT INHIBIT METABOLIC PROCESSES OF OTHER ORGANISMS 890
35.7 COMMERCIAL EXPLOITATION OF BACTERIAL ENZYMES 893 35.8 HETEROLOGOUS
PROTEINS ARE PRODUCED BY RECOMBINANT DNA TECHNOLOGY 896 36 PROKARYOTES
IN ENVIRONMENTAL PROCESSES B. SCHINK 36.1 WASTEWATER TREATMENT
INTENSIFIES NATURAL BIOLOGICAL DEGRADATION PROCESSES 901 36.2 COMPOSTING
BECOMES FASHIONABLE AGAIN ... 907 36.3 DRINKING WATER ALSO MAY REQUIRE
MICROBIOLOGICAL PRETREATMENT 908 36.4 EXHAUST-GAS TREATMENT, A FURTHER
WORKING AREA FOR AEROBIC BACTERIA 908 900 36.5 BIOREMEDIATION OF SOIL IS
A GROWING MARKET. 908 36.6 BIOSENSORS EXPLOIT THE SPECIFICITY AND
DIVERSITY OF BIOCHEMICAL REACTIONS 910 36.7 LITHOTROPHIC BACTERIA ARE
ACTIVE IN METAL MINING 911 37 37.1 37.2 37.3 37.4 PROKARYOTES AND MAN:
CHANCES, PROMISES, AND RISKS A. PUHLER 913 FROM THE PAST TO THE FUTURE:
SEQUENCE ANALYSIS OF TOTAL BACTERIAL GENOMES WILL REVOLUTIONIZE APPLIED
MICROBIOLOGY 913 FUTURE ASPECTS OF PROKARYOTES IN MEDICINE: NEW DRUGS,
VACCINES, AND DIAGNOSTIC TOOLS WILL BE BASED ON KNOWLEDGE OF MOLECULAR
MECHANISMS 914 FUTURE ASPECTS OF PROKARYOTES IN AGRICULTURE:
PHYTOPATHOGENIC AND BENEFICIAL BACTERIA REQUIRE MORE FUNDAMENTAL
RESEARCH 915 FUTURE ASPECTS OF PROKARYOTES IN ENVIRONMENTAL PROCESSES:
BASIC QUESTIONS CONCERNING BIODIVERSITY, COMMUNITY STRUCTURES, AND
CULTURE CONDITIONS HAVE NOT YET BEEN ANSWERED 915 37.5 FUTURE ASPECTS OF
PROKARYOTES IN INDUSTRIAL PRODUCTION: APPROPRIATE PRODUCTION STRAINS
WILL BE GENETICALLY ENGINEERED FOR AN OPTIMAL METABOLIC AND PROCESS
DESIGN 916 37.6 POTENTIAL RISKS AND RISK MANAGEMENT OF GENETICALLY
ENGINEERED BACTERIA: REGULATIONS AND LAWS HAVE BEEN ESTABLISHED
WORLDWIDE 918 INDEX 921
|
any_adam_object | 1 |
building | Verbundindex |
bvnumber | BV012384436 |
classification_rvk | WF 1000 WF 1700 WF 5000 |
classification_tum | BIO 250f BIO 310f BIO 502f |
ctrlnum | (OCoLC)231784672 (DE-599)BVBBV012384436 |
dewey-full | 579.3 |
dewey-hundreds | 500 - Natural sciences and mathematics |
dewey-ones | 579 - Microorganisms, fungi & algae |
dewey-raw | 579.3 |
dewey-search | 579.3 |
dewey-sort | 3579.3 |
dewey-tens | 570 - Biology |
discipline | Biologie |
edition | 1. publ. |
format | Book |
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id | DE-604.BV012384436 |
illustrated | Illustrated |
indexdate | 2024-07-09T18:26:40Z |
institution | BVB |
isbn | 3131084111 0632053577 9780632053575 |
language | German |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-008400753 |
oclc_num | 231784672 |
open_access_boolean | |
owner | DE-20 DE-19 DE-BY-UBM DE-29T DE-703 DE-12 DE-1028 DE-91G DE-BY-TUM DE-M490 DE-355 DE-BY-UBR DE-Er8 DE-634 DE-83 DE-526 DE-91S DE-BY-TUM DE-11 DE-188 |
owner_facet | DE-20 DE-19 DE-BY-UBM DE-29T DE-703 DE-12 DE-1028 DE-91G DE-BY-TUM DE-M490 DE-355 DE-BY-UBR DE-Er8 DE-634 DE-83 DE-526 DE-91S DE-BY-TUM DE-11 DE-188 |
physical | XXVII, 955 S. zahlr. Ill., graph. Darst. |
publishDate | 1999 |
publishDateSearch | 1999 |
publishDateSort | 1999 |
publisher | Thieme [u.a.] |
record_format | marc |
spelling | Biology of the prokaryotes 150 tables ed. by Joseph W. Lengeler ... 1. publ. Stuttgart [u.a.] Thieme [u.a.] 1999 XXVII, 955 S. zahlr. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Literaturangaben Prokaryotes cabt Prokaryoten (DE-588)4201051-2 gnd rswk-swf Prokaryoten (DE-588)4201051-2 s DE-604 Lengeler, Joseph W. Sonstige oth HEBIS Datenaustausch Mainz application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008400753&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
spellingShingle | Biology of the prokaryotes 150 tables Prokaryotes cabt Prokaryoten (DE-588)4201051-2 gnd |
subject_GND | (DE-588)4201051-2 |
title | Biology of the prokaryotes 150 tables |
title_auth | Biology of the prokaryotes 150 tables |
title_exact_search | Biology of the prokaryotes 150 tables |
title_full | Biology of the prokaryotes 150 tables ed. by Joseph W. Lengeler ... |
title_fullStr | Biology of the prokaryotes 150 tables ed. by Joseph W. Lengeler ... |
title_full_unstemmed | Biology of the prokaryotes 150 tables ed. by Joseph W. Lengeler ... |
title_short | Biology of the prokaryotes |
title_sort | biology of the prokaryotes 150 tables |
title_sub | 150 tables |
topic | Prokaryotes cabt Prokaryoten (DE-588)4201051-2 gnd |
topic_facet | Prokaryotes Prokaryoten |
url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008400753&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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