The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase
Abstract In contrast to the widely accepted consensus of the existence of a single RNA polymerase in bacteria, several actinomycetes have been recently shown to possess two forms of RNA polymerases due the to co-existence of two rpoB paralogs in their genome. However, the biological significance of...
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oai:doaj.org-article:e757f8c8ad234a29bc890b46372dd1352021-12-02T12:32:08ZThe complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase10.1038/s41598-016-0025-02045-2322https://doaj.org/article/e757f8c8ad234a29bc890b46372dd1352016-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-016-0025-0https://doaj.org/toc/2045-2322Abstract In contrast to the widely accepted consensus of the existence of a single RNA polymerase in bacteria, several actinomycetes have been recently shown to possess two forms of RNA polymerases due the to co-existence of two rpoB paralogs in their genome. However, the biological significance of the rpoB duplication is obscure. In this study we have determined the genome sequence of the lipoglycopeptide antibiotic A40926 producer Nonomuraea gerenzanensis ATCC 39727, an actinomycete with a large genome and two rpoB genes, i.e. rpoB(S) (the wild-type gene) and rpoB(R) (the mutant-type gene). We next analyzed the transcriptional and metabolite profiles in the wild-type gene and in two derivative strains over-expressing either rpoB(R) or a mutated form of this gene to explore the physiological role and biotechnological potential of the “mutant-type” RNA polymerase. We show that rpoB(R) controls antibiotic production and a wide range of metabolic adaptive behaviors in response to environmental pH. This may give interesting perspectives also with regard to biotechnological applications.Valeria D’ArgenioMauro PetrilloDaniela PasanisiCaterina PagliaruloRoberta ColicchioAdelfia TalàMaria Stella de BiaseMario ZanfardinoEmanuela ScolamieroChiara PagliucaAntonio GaballoAnnunziata Gaetana CicatielloPiergiuseppe CantielloIrene PostiglioneBarbara NasoAngelo BocciaMiriana DuranteLuca CozzutoPaola SalvatoreGiovanni PaolellaFrancesco SalvatorePietro AlifanoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 6, Iss 1, Pp 1-13 (2016) |
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Medicine R Science Q Valeria D’Argenio Mauro Petrillo Daniela Pasanisi Caterina Pagliarulo Roberta Colicchio Adelfia Talà Maria Stella de Biase Mario Zanfardino Emanuela Scolamiero Chiara Pagliuca Antonio Gaballo Annunziata Gaetana Cicatiello Piergiuseppe Cantiello Irene Postiglione Barbara Naso Angelo Boccia Miriana Durante Luca Cozzuto Paola Salvatore Giovanni Paolella Francesco Salvatore Pietro Alifano The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase |
description |
Abstract In contrast to the widely accepted consensus of the existence of a single RNA polymerase in bacteria, several actinomycetes have been recently shown to possess two forms of RNA polymerases due the to co-existence of two rpoB paralogs in their genome. However, the biological significance of the rpoB duplication is obscure. In this study we have determined the genome sequence of the lipoglycopeptide antibiotic A40926 producer Nonomuraea gerenzanensis ATCC 39727, an actinomycete with a large genome and two rpoB genes, i.e. rpoB(S) (the wild-type gene) and rpoB(R) (the mutant-type gene). We next analyzed the transcriptional and metabolite profiles in the wild-type gene and in two derivative strains over-expressing either rpoB(R) or a mutated form of this gene to explore the physiological role and biotechnological potential of the “mutant-type” RNA polymerase. We show that rpoB(R) controls antibiotic production and a wide range of metabolic adaptive behaviors in response to environmental pH. This may give interesting perspectives also with regard to biotechnological applications. |
format |
article |
author |
Valeria D’Argenio Mauro Petrillo Daniela Pasanisi Caterina Pagliarulo Roberta Colicchio Adelfia Talà Maria Stella de Biase Mario Zanfardino Emanuela Scolamiero Chiara Pagliuca Antonio Gaballo Annunziata Gaetana Cicatiello Piergiuseppe Cantiello Irene Postiglione Barbara Naso Angelo Boccia Miriana Durante Luca Cozzuto Paola Salvatore Giovanni Paolella Francesco Salvatore Pietro Alifano |
author_facet |
Valeria D’Argenio Mauro Petrillo Daniela Pasanisi Caterina Pagliarulo Roberta Colicchio Adelfia Talà Maria Stella de Biase Mario Zanfardino Emanuela Scolamiero Chiara Pagliuca Antonio Gaballo Annunziata Gaetana Cicatiello Piergiuseppe Cantiello Irene Postiglione Barbara Naso Angelo Boccia Miriana Durante Luca Cozzuto Paola Salvatore Giovanni Paolella Francesco Salvatore Pietro Alifano |
author_sort |
Valeria D’Argenio |
title |
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase |
title_short |
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase |
title_full |
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase |
title_fullStr |
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase |
title_full_unstemmed |
The complete 12 Mb genome and transcriptome of Nonomuraea gerenzanensis with new insights into its duplicated “magic” RNA polymerase |
title_sort |
complete 12 mb genome and transcriptome of nonomuraea gerenzanensis with new insights into its duplicated “magic” rna polymerase |
publisher |
Nature Portfolio |
publishDate |
2016 |
url |
https://doaj.org/article/e757f8c8ad234a29bc890b46372dd135 |
work_keys_str_mv |
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