Discovery of a two-component monooxygenase SnoaW/SnoaL2 involved in nogalamycin biosynthesis.
- V. SiitonenBastian BlauenburgP. KallioP. MäntsäläM. Metsä‐Ketelä
- 25 May 2012
Biology, Chemistry
It is demonstrated that inactivation of either snoaL2 or snoaW resulted in accumulation of two nonhydroxylated metabolites, nogalamycinone and a novel anthracycline 3',4'-demethoxy-nogalose-nogialamyzinone.
Genotyping-Guided Discovery of Persiamycin A From Sponge-Associated Halophilic Streptomonospora sp. PA3
- S. MatroodiV. SiitonenB. BaralK. YamadaA. AkhgariM. Metsä‐Ketelä
- 9 June 2020
Environmental Science, Biology
The work demonstrates the use of multivariate data and underexplored ecological niches to guide the drug discovery process for antibiotics and anticancer agents.
Photosynthetically produced sucrose by immobilized Synechocystis sp. PCC 6803 drives biotransformation in E. coli
- G. TóthV. Siitonen Y. Allahverdiyeva
- 1 December 2022
Environmental Science, Chemistry
It is demonstrated that cell entrapment in Ca 2+ -alginate beads is an effective method to prolong sucrose production by the engineered cyanobacteria, while allowing efficient separation of the cells from the medium.
Laboratory course on Streptomyces genetics and secondary metabolism
- V. SiitonenKaj RätyM. Metsä‐Ketelä
- 10 September 2016
Engineering
The course combines genetic modification of Streptomyces; growing of the strain and protoplast preparation, plasmid isolation by alkaline lysis and phenol precipitation, digestions, and ligations prior to protoplast transformation, as well as investigating the secondary metabolites produced by the strains.
Divergent non-heme iron enzymes in the nogalamycin biosynthetic pathway
- V. SiitonenB. SelvarajL. NiiranenY. LindqvistG. SchneiderM. Metsä‐Ketelä
- 25 April 2016
Chemistry, Biology
It is demonstrated that the proteins are evolutionarily related and that only a limited set of amino acid changes in the active sites are responsible for the switch in chemistry, encouraging for future research because it indicates that protein engineering could lead to generation of novel compounds with improved biological activities.
Co-factor independent oxidases ncnN and actVA-3 are involved in the dimerization of benzoisochromanequinone antibiotics in naphthocyclinone and actinorhodin biosynthesis
- B. BaralS. Matroodi M. Metsä‐Ketelä
- 21 November 2023
Chemistry, Biology
The sequenced genome of S. arenae DSM40737 was used to identify the naphthocyclinone gene cluster and established heterologous production in S. albus J1074, suggesting that dimerization of benzoisochromanequinone polyketides require two-component reductase-oxidase systems.
The Rieske Oxygenase SnoT Catalyzes 2′′‐Hydroxylation of l‐Rhodosamine in Nogalamycin Biosynthesis
- Benjamin Nji WandiV. SiitonenK. PalmuM. Metsä‐Ketelä
- 17 June 2020
Chemistry, Biology
It is demonstrated that the Rieske enzyme SnoT catalyzes 2′′‐hydroxylation of l‐rhodosamine as an initial post‐glycosylation step in nogalamycin biosynthesis, and that the reaction order continues with 2–5′′ carbocyclization and 4′′ epimerization by the non‐heme iron and 2‐oxoglutarate‐dependent enzymes SnoK and SnoN, respectively.
Crystal structure of the epimerase SnoN in complex with Fe3+, alpha ketoglutarate and nogalamycin RO
- B. SelvarajY. LindqvistV. SiitonenM. Metsa-KetelaG. Schneider
- 11 May 2016
Chemistry, Biology
Mapping Nanocellulose- and Alginate-Based Photosynthetic Cell Factory Scaffolds: Interlinking Porosity, Wet Strength, and Gas Exchange
- Tuukka LeväV. Rissanen T. Tammelin
- 29 June 2023
Environmental Science, Materials Science
To develop efficient solid-state photosynthetic cell factories for sustainable chemical production, we present an interdisciplinary experimental toolbox to investigate and interlink the structure,…
Discovery of the Showdomycin Gene Cluster from Streptomyces showdoensis ATCC 15227 Yields Insight into the Biosynthetic Logic of C-Nucleoside Antibiotics.
- K. PalmuPetja Rosenqvist M. Metsä‐Ketelä
- 27 April 2017
Chemistry, Biology
Nucleoside antibiotics are a large class of pharmaceutically relevant chemical entities, which exhibit a broad spectrum of biological activities. Most nucleosides belong to the canonical N-nucleoside…
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