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Schwientek, Patrick: Genomics and transcriptomics of the industrial acarbose producer Actinoplanes sp. SE50/110. 2012
Inhalt
1 Introduction
1.1 The genus Actinoplanes
1.2 The strain Actinoplanes sp. SE50/110
1.3 The secondary metabolite acarbose, its relevance, and mode of action
1.4 The biosynthesis of acarbose in Actinoplanes sp. SE50/110
1.5 Industrial development and fermentation of acarbose
1.6 Bacterial genome sequencing approaches
1.7 Bacterial genome annotation strategies
1.8 Means of bacterial transcriptome analysis
1.9 Motivation and aims of this thesis
2 Materials and Methods
2.1 Acquisition of the strain Actinoplanes sp. SE50/110
2.2 Genomic DNA-sequencing methods
2.2.1 Cultivation of Actinoplanes sp. SE50/110 for DNA-sequencing
2.2.2 Isolation of genomic DNA from Actinoplanes sp. SE50/110
2.2.3 Pyrosequencing of the Actinoplanes sp. SE50/110 genomic DNA on the Genome Sequencer FLX
2.3 Genome assembly and mapping techniques
2.3.1 Genome assembly
2.3.2 Read mapping on the acarbose gene cluster
2.4 Genome finishing methods
2.4.1 Construction of a fosmid library for the Actinoplanes sp. SE50/110 genome finishing
2.4.2 Polymerase chain reactions
2.4.3 Sanger sequencing of PCR products and terminal insert sequences from the Actinoplanes sp. SE50/110 fosmid library
2.4.4 Finishing of the Actinoplanes sp. SE50/110 genome sequence by manual assembly
2.5 Computational genome annotation
2.5.1 Prediction of coding sequences on the Actinoplanes sp. SE50/110 genome sequence
2.5.2 Functional annotation of the identified CDS on the Actinoplanes sp. SE50/110 genome
2.5.3 Phylogenetic analyses
2.6 RNA-sequencing and analysis
2.6.1 Cultivation of Actinoplanes sp. SE50/110 for RNA-sequencing
2.6.2 Total RNA isolation from Actinoplanes sp. SE50/110
2.6.3 Preparation of cDNA libraries and high-throughput sequencing
2.6.4 Determination of cell dry weights of Actinoplanes cultures
2.6.5 Quantification of acarbose in the supernatant of Actinoplanes cultures by HPLC and UV detection
2.6.6 Bioinformatic analysis of RNA-seq results
2.7 Gas-chromatographic analysis of the anti-self-annealing additive
3 Results
3.1 Solving the high-GC problem for Actinoplanes sp. SE50/110 genome sequencing
3.1.1 Analysis of gap regions resulted from standard PE sequencing
3.1.2 The gaps in the Actinoplanes sp. SE50/110 acarbose gene cluster are due to an extremely low read coverage
3.1.3 The gaps in the acarbose gene cluster are characterized by secondary structure formation
3.1.4 Adapted sequencing conditions solved the high-GC problem
3.2 The complete genome sequence of Actinoplanes sp. SE50/110
3.2.1 Assembly of the Actinoplanes sp. SE50/110 draft genome sequence
3.2.2 Finishing of the draft genome sequence
3.2.3 Annotation of the complete genome sequence
3.3 Discoveries of the Actinoplanes sp. SE50/110 genome
3.3.1 General features of the Actinoplanes sp. SE50/110 genome
3.3.2 Phylogenetic analysis of the Actinoplanes sp. SE50/110 16S rDNA reveals highest similarity to Actinoplanes utahensis
3.3.3 Comparative genome analysis indicates 50% singletons in the Actinoplanes sp. SE50/110 genome.
3.3.4 The high quality genome sequence of Actinoplanes sp. SE50/110 corrects the previously sequenced acarbose cluster.
3.3.5 Several genes of the acarbose gene cluster are also found in other locations of the genome.
3.3.6 Trehalose synthesis in Actinoplanes sp. SE50/110
3.3.7 The Actinoplanes sp. SE50/110 genome hosts an integrative and conjugative element
3.3.8 Four putative antibiotic production gene clusters were found in the Actinoplanes sp. SE50/110 genome sequence
3.4 RNA-sequencing of the Actinoplanes sp. SE50/110 transcriptome
3.4.1 Cultivation of Actinoplanes sp. SE50/110 for transcriptome analysis
3.4.2 Improving the Actinoplanes genome annotation by RNA-seq
3.4.3 Expression analysis of Actinoplanes sp. SE50/110 grown in three different cultivation media
4 Discussion
4.1 Establishment of the complete Actinoplanes sp. SE50/110 genome sequence
4.2 Annotation of the Actinoplanes sp. SE50/110 genome sequence
4.3 New insights related to the acarbose metabolism
4.3.1 Acarbose re-import after exclusion of acbHFG
4.3.2 Putative formation of component C by trehalose synthases
4.4 The actinomycete integrative and conjugative element pACPL
4.5 The putative antibiotic gene clusters of Actinoplanes sp. SE50/110
4.6 Transcriptome analyses of Actinoplanes sp. SE50/110
4.6.1 Improvement of genome annotation by RNA-seq
4.6.2 Differential expression testing by RNA-seq
4.6.3 Short assessment of computational methods for bacterial RNA-seq analysis
5 Conclusions and Outlook
Bibliography
A Appendix
A.1 Supplementary figures
A.2 Supplementary tables