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Javier Santos-Aberturas

Researcher at John Innes Centre

Publications -  29
Citations -  1077

Javier Santos-Aberturas is an academic researcher from John Innes Centre. The author has contributed to research in topics: Streptomyces natalensis & Gene. The author has an hindex of 19, co-authored 28 publications receiving 826 citations. Previous affiliations of Javier Santos-Aberturas include University of Greifswald & University of León.

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PimM, a PAS domain positive regulator of pimaricin biosynthesis in Streptomyces natalensis.

TL;DR: Results indicate that PimM plays its regulatory role independently of PimR, the first pathway-specific regulator of pimaricin biosynthesis, and the genes responsible for initiation and first elongation cycles of polyketide chain extension are among the major targets for regulation.
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Uncovering the unexplored diversity of thioamidated ribosomal peptides in Actinobacteria using the RiPPER genome mining tool.

TL;DR: RiPPER, a new tool for the family-independent identification of RiPP precursor peptides, is described and it is shown that previously undescribed RiPP gene clusters encoding YcaO and TfuA proteins are widespread in Actinobacteria and encode a highly diverse landscape of precursor peptide that are predicted to make thioamidated RiPPs.
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Biotechnological production and application of the antibiotic pimaricin: biosynthesis and its regulation

TL;DR: The molecular genetics, uses, mode of action, analogue generation, regulation and strategies for increasing pimaricin production yields are described and discussed.
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Fully automatized high-throughput enzyme library screening using a robotic platform.

TL;DR: The fully automatized robotic platform enables proper monitoring and control of growth conditions in the microtiter plate format to ensure precise enzyme production for the interrogation of enzyme mutant libraries, protein stability tests and multiple assay screenings.
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Cholesterol Oxidases Act as Signaling Proteins for the Biosynthesis of the Polyene Macrolide Pimaricin

TL;DR: Gene-inactivation and -complementation experiments revealed that pimE encodes a functional cholesterol oxidase and, surprisingly, that it is also involved in pimaricin biosynthesis, which broadens the scope of the biological functions for this type of oxidase.