Iron uptake in Gram-negative bacteria involves four distinct steps: (i) siderophore synthesis, (ii) siderophore secretion into the extracellular space, (iii) iron chelation by the siderophores, and (iv) siderophore/iron uptake via complexes in the outer membrane and the intermembrane space as well as in the plasma membrane. This process is well characterized for some proteobacterial systems, but largely unexplored and scarcely investigated in cyanobacteria such as the heterocyst-forming cyanobacterium Anabaena sp. PCC 7120. Two putative siderophore synthesis clusters have been recently identified in this cyanobacterium. In addition, the export system for the main siderophore, schizokinen, secreted by Anabaena sp. PCC 7120 was described as well as the outer membrane transporter for its import from the extracellular space. We present the identification of components of three additional systems involved in siderophore-mediated iron uptake under iron-limiting conditions, namely TonB3, the ExbB3/ExbD3 and the Fhu systems. The transcription level of these genes is elevated under iron limitations and decreased under excess iron, while the expression levels of other members of these gene families and systems are impacted in distinct ways by other environmental conditions. Mutants of the tonB3, exbB3/exbD3 and fhu genes show an iron starvation phenotype. Thus, Anabaena sp. has a similar, yet distinct system for siderophore-dependent iron uptake compared with other proteobacteria.
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http://dx.doi.org/10.1111/j.1462-2920.2011.02619.x | DOI Listing |
Int J Biol Macromol
December 2024
Molecular Biology Section, Department of Botany, Institute of Science, Banaras Hindu University, Varanasi 221005, India. Electronic address:
Native amine dehydrogenases (AmDHs) are rare and typically have narrow substrate specificity and low processivity. Therefore, they are often modified using protein engineering for industrial and pharmaceutical applications. This study presents identification and characterization of a novel native amine dehydrogenase (AmDH) encoding WD40 protein (All1750) from Anabaena PCC 7120.
View Article and Find Full Text PDFMol Microbiol
January 2025
Instituto de Bioquímica Vegetal y Fotosíntesis, CSIC and Universidad de Sevilla, Seville, Spain.
Cyanobacteria developed oxygenic photosynthesis and represent the phylogenetic ancestors of chloroplasts. The model strain Anabaena sp. strain PCC 7120 grows as filaments of communicating cells and can form heterocysts, cells specialized for N fixation.
View Article and Find Full Text PDFMicrobiol Res
January 2025
State Key Laboratory of Freshwater Ecology and Biotechnology, Key Laboratory of Algal Biology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430070, Hubei, China; Hubei Hongshan Laboratory, Wuhan 430070, Hubei, China. Electronic address:
PacR (All3953) has previously been identified as a global transcriptional regulator of carbon assimilation in cyanobacteria. In the facultative diazotrophic and filamentous cyanobacterium Anabaena PCC 7120 (Anabaena), inactivation of pacR has been shown to affect cell growth under various conditions. Nitrogen fixation in Anabaena occurs in heterocysts, cells differentiated semiregularly along the filaments following deprivation of combined nitrogen such as nitrate or ammonium.
View Article and Find Full Text PDFNPJ Microgravity
November 2024
Center of Applied Space Technology and Microgravity (ZARM), University of Bremen, Bremen, Germany.
In situ resource utilization systems based on cyanobacteria could support the sustainability of crewed missions to Mars. However, their resource-efficiency will depend on the extent to which gases from the Martian atmosphere must be processed to support cyanobacterial growth. The main purpose of the present work is to help assess this extent.
View Article and Find Full Text PDFJ Bacteriol
October 2024
School of Biological and Behavioural Sciences, Queen Mary University of London, London, United Kingdom.
Heterocyst-forming cyanobacteria such as () sp. PCC 7120 exhibit extensive remodeling of their thylakoid membranes during heterocyst differentiation. Here we investigate the sites of translation of thylakoid membrane proteins in vegetative cells and developing heterocysts, using mRNA fluorescent hybridization (FISH) to detect the location of specific mRNA species.
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