PCC 7120, it has indeed GSI-IX ic50 been shown that the amount of DNA in the two newborn daughter cells after cell division is not always identical, but can vary (Hu et al., 2007; Schneider et al., 2007). An additional advantage is gene redundancy,

which opens the possibility that under unfavorable conditions, mutations are induced in some genome copies, whereas the wildtype information is retained in others. It has indeed been shown that heterozygous cells of S. elongatus PCC 7942 and of Synechocystis PCC 6803 can be selected, at least under laboratory conditions (Labarre et al., 1989; Spence et al., 2004; Takahama et al., 2004; Nodop et al., 2008). Heterozygous strains have also been selected of two halophilic and methanogenic archaea, Haloferax volcanii and Methanococcus maripaludis. In both cases, it was shown that in the absence of selection gene conversion leads to the equalization of genomes and reappearance of homozygous cells (Hildenbrand et al., 2011; Lange et al., 2011). By analogy, we predict that gene conversion also operates in oligo- and

polyploid species of cyanobacteria. The higher efficiency of gene replacement with linear DNA compared with circular DNA in Synechocystis PCC 6803 indicates that this is really the case (Labarre et al., 1989). This work was supported by grant So264/16-1 of the German Research Council (Deutsche Forschungsgemeinschaft). We thank Annegret Wilde (University of Giessen, Germany) for the motile and the GT Synechocystis PCC 6803 strains, Wolfgang R. Hess for S. elongatus Selleckchem Regorafenib PCC 7942 and Synechococcus sp. WH7803, and both for very valuable advice concerning growth of cyanobacteria. We thank Enrico Schleiff for the possibility to grow cyanobacterial cultures in his light incubator. We are grateful to two reviewers who were patient with us as non-experts of cyanobacteria,

and gave us very good suggestions and literature references. “
“1-Aminocyclopropane-1-carboxylate (ACC) deaminase is commonly produced by plant growth-promoting rhizobacteria (PGPR) and has been suggested to facilitate the growth and stress tolerance of hosts via a reduction in levels of ethylene. However, the regulatory mechanism of ACC deaminase (AcdS) protein within host plant cells is largely unknown. Here, we demonstrated beneficial effects and post-translational modification of PGPR-originated AcdS triclocarban proteins in plants. Compared with the wild-type, transgenic Arabidopsis expressing the Pseudomonas fluorescens acdS (PfacdS) gene displayed increased root elongation and reduced sensitivity to 10 μM exogenous ACC, an ethylene precursor. Arabidopsis expressing PfacdS also showed increased tolerance to high salinity (150 mM NaCl). PfAcdS proteins accumulated in transgenic Arabidopsis were rapidly degraded, which was potentially mediated by the 26S proteasome pathway. The degradation of PfAcdS was alleviated in the presence of exogenous ACC.