Abstract
Streptomyces ghanaensis produces the antibiotic moenomycin A, which is the only known direct inhibitor of bacterial peptidoglycan glycosyltransferases (transglycosylases). Recent progress in understanding moenomycin biosynthesis opens the door to the generation of novel moenomycins via biocombinatorial approaches. To realize the promise of such an approach, one needs better knowledge of the S. ghanaensis genome and diverse genetic tools for stable expression of recombinant constructs in this strain. In this respect, we report the intergeneric Escherichia coli-S. ghanaensis conjugal transfer of plasmids pRT801 and pSOK804 based on the actinophage BT1 and VWB integrase systems, respectively. The attB sites for these two plasmids and for pSET152 were characterized. In particular, sequencing revealed that a putative Arg-tRNA gene serves as an integration site for both phage VWB and pSAM2-like actinomycete integrative and conjugative element recently suggested to be widespread and functional in actinomycetes. The stability of the studied plasmids and their neutrality with respect to antibiotic production warrant their use for manipulations of S. ghanaensis genome.
MeSH Terms
Bambermycins/chemistry,metabolism
Base Sequence
Escherichia coli/genetics
Gene Components
Gene Transfer Techniques
Genetic Engineering/methods
Genetic Vectors/genetics
Molecular Sequence Data
Molecular Structure
RNA, Transfer, Arg/genetics
Sequence Analysis, DNA
Streptomyces/genetics
Chemicals
RNA, Transfer, Arg
Bambermycins
moenomycin A
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ostash Bohdan
Department of Genetics and Biotechnology, Ivan Franko National University of L'viv, Grushevskogo st., 79005 L'viv, Ukraine.
Makitrinskyy Roman
Walker Suzanne
Fedorenko Victor
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