The loss of the phoS periplasmic protein leads to a change in the specificity of a constitutive inorganic phosphate transport system in Escherichia coli

The phoS periplasmic protein, implicated in alkaline phosphatase regulation, is shown to be involved in inorganic phosphate (Pi) transport in $\text{E. coli}$. Although $\text{pho}\text{S}{}^{\mathrm{?}}$ cells dependent upon the PST system for Pi transport can grow in minimal medium with 1 mM Pi as source of phosphorus, the affinity of these cells for Pi is greatly reduced; Km = 18 μM compared with Km = 0.4 μM for $\text{phoS}{}^{\mathrm{+}}$ cells. $\text{pho}\text{S}{}^{\mathrm{?}}$ cells dependent upon the PST Pi transport system acquire the ability to accumulate Asi from the medium in contrast to $\text{pho}\text{S}{}^{\mathrm{+}}$ cells which exclude this toxic anion. It would appear that the periplasmic phoS protein is not essential for Pi accumulation but is involved in maintaining the specificity of the PST Pi transport system.     

A new Pseudophoxinus (Teleostei,Cyprinidae) species from Asi River Drainage (Turkey)

Pseudophoxinus turani sp. n. is described from the İncesu Spring (Hassa-Hatay) drainage of Asi River, Turkey. It is distinguished from other Eastern Mediterranean Region Pseudophoxinus species by a combination of characters: lateral line incomplete, with 12–25 (commonly 16–21) perforated scales and 38–46+2-3 scales in lateral series (commonly 41–44+2-3); 10–11 scale rows between the lateral line and dorsal-fin origin; 3–4 scale rows between the lateral line and the pelvic–fin origin; dorsal fin with 7½ branched rays; anal fin commonly with 7½ branched rays; 8-11gill rakers on the first branchial arch; dorsal profile markedly convex with marked hump at the nape, ventral profile less convex than dorsal profile; a small, irregular, black blotch on the base of the caudal fin; mouth terminal, with slightly distinct chin, its corner not reaching vertical through anterior margin of eye; snout somewhat long, with rounded tip; and its length greater than eye diameter.     

Mitochondrial Ca transport and permeability transition in zebrafish (Danio rerio)

We have studied mitochondrial Ca²⁺ transport and the permeability transition (PT) in the teleost zebrafish (Danio rerio), a key model system for human diseases. Permeabilized zebrafish embryo cells displayed a mitochondrial energy-dependent Ca²⁺ uptake system that, like the Ca²⁺ uniporter of mammals, was inhibited by ruthenium red. Zebrafish mitochondria underwent a Ca²⁺-dependent PT that displayed Pi-dependent desensitization by cyclosporin A, and responded appropriately to key modulators of the mammalian PT pore (voltage, pH, ubiquinone 0, dithiol oxidants and cross linkers, ligands of the adenine nucleotide translocator, arachidonic acid). Opening of the pore was documented in intact cells, where it led to death that could largely be prevented by cyclosporin A. Our results represent a necessary step toward the use of zebrafish for the screening and validation of PTP inhibitors of potential use in human diseases, as recently shown for collagen VI muscular dystrophy [Telfer et al., 2010].