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Hellweg, Matthias: Molecular biological and biochemical studies of proteolytic enzymes of the cereal pathogen Fusarium graminearum. 2003
Inhalt
Contents
Abbreviations
Introduction
Introduction to plant disease resistance mechanisms
The structure of plant cell walls
Cell wall degrading enzymes
General classification of proteases
Fusarium graminearum
Objectives of the present work
Materials and Methods
Materials
Chemicals and Materials
Organisms – growth conditions and strain maintenance
Fungal isolates
Plant cultivars
Bacteria
Methods
Cultivation of Fusarium graminearum in submerged culture
CM-medium, minimal medium and protease induction medium
Preculture
Induction of conidia
Induction of protease secretion
Growth rate and kinetics of protease secretion
Kinetics of initial protease secretion – Mass inoculation
Variations in protein derived nitrogen levels
Variations in carbohydrate levels
Isolated wheat cell wall material as substrate
Cultivation of Fusarium graminearum on agar plates
In planta cultivation – Detached leaf petri dish assay
Protein biochemical methods
Photometric assay for protease activity
pH-profile and temperature optimum
Inhibitor studies
Cation exchange perfusion chromatography
SDS polyacrylamide gel elecrophoresis (SDS-PAGE)
'Slow' Coomassie staining of acrylamide gels
Silver staining of acrylamide gels
Standard zymography
Blotting zymography
Molecular biology
Isolation of fungal DNA
Standard PCR
Touch-down PCR
Inverse PCR
TAIL PCR
Standard agarose gel electrophoresis
Purification of PCR fragments
Cloning of PCR fragments and colony PCR
Plasmid purification and sequencing of cloned PCR fragments
Isolation of fungal RNA
cDNA production and RT-PCR
Quantitative expression analysis
Computer aided methods
Documentation of polyacrylamide gels, agarose gels, macroscopic and microscopic images
Analysis of DNA and amino acid sequences
Databases
Sequence alignment
Prediction of protein characteristics based on amino acid sequences
Results
General characterization of fungal growth
Growth on CM agar
Submerged culture in CM-medium
Formation of conidia
Optimization of the photometric protease assay
Development of protease induction medium
Characterization of growth in protease induction medium
Growth on PI-agar compared to CM- and minimal-agar
Submerged culture in PI-medium compared to CM- and minimal medium
Kinetics of protease secretion
Overview of protease secretion – daily samples
Basic characterization of the protease activity induced in PI-medium
pH-optimum
Temperature optimum
Inhibitor studies
Kinetics of initial protease secretion – Mass inoculation
Variations in nitrogen and carbohydrate levels – Mass inoculation
Growth in CM- and PI-medium – Mass inoculation
pH of the medium during cultivation in PI- and pPI-medium with variations in carbon levels – Mass inoculation
Protease activity and pH of the medium during growth in minimal medium containing wheat cell wall material – Mass inoculation
SDS-PAGE of crude media samples
Partial purification of a protease from PI-medium
Cation exchange chromatography
SDS-PAGE and zymography of FPLC fractions
Cloning and sequencing of a protease gene
Molecular characterization of the obtained gene
Molecular characterization of the 5'-flanking region of prt1
Cloning and sequencing of a cDNA fragment of prt1
Qualitative expression studies
Growth of Fusarium graminearum in CM- and PI-medium
Growth of Fusarium graminearum in planta – detached leaf petri dish assay
Discussion
Selection and evaluation of a suitable proteinacious substrate for protease induction
Macroscopic and microscopic characterization of growth
Protease induction - Time course, basic characterization of proteolytic activity and regulation by carbon and nitrogen availability
Protease induction – Electrophoretic analysis of substrate digestion and identification of induced proteases
Protease induction during cultivation with cell wall material?
Prt1 – a gene encoding a subtilisin-like protease
Comparative overview and outlook
Abstract
Zusammenfassung
References
Appendix
Thank you
Curriculum vitae