lac Repressor Is an Antivirulence Factor of Salmonella enterica: Its Role in the Evolution of Virulence in Salmonella

The genus Salmonella includes many pathogens of great medical and veterinary importance. Bacteria belonging to this genus are very closely related to those belonging to the genus Escherichia. lacZYA operon and lacI are present in Escherichia coli, but not in Salmonella enterica. It has been proposed that Salmonella has lost lacZYA operon and lacI during evolution. In this study, we have investigated the physiological and evolutionary significance of the absence of lacI in Salmonella enterica. Using murine model of typhoid fever, we show that the expression of Lacl causes a remarkable reduction in the virulence of Salmonella enterica. Lacl also suppresses the ability of Salmonella enterica to proliferate inside murine macrophages. Microarray analysis revealed that Lacl interferes with the expression of virulence genes of Salmonella pathogenicity island 2. This effect was confirmed by RT-PCR and Western blot analysis. Interestingly, we found that SBG0326 of Salmonella bongori is homologous to lacI of Escherichia coli. Salmonella bongori is the only other species of the genus Salmonella and it lacks the virulence genes of Salmonella pathogenicity island 2. Overall, our results demonstrate that Lacl is an antivirulence factor of Salmonella enterica and suggest that absence of lacI has facilitated the acquisition of virulence genes of Salmonella pathogenicity island 2 in Salmonella enterica making it a successful systemic pathogen.

A hypothesis on a specific sequence-dependent conformation of DNA and its relation to the binding of the lac-repressor protein

The structure and properties of the double-helical form of the alternating copolymer poly(dA-dT) are considered. Different lines of evidence are interpreted in terms of a structure in which every second phosphate-diester linkage has a conformation different from that of the normal B form. A rationale for this “alternating-B” structure is given which provides an explanation for the effects of chemical modifications of the T residues on the binding of the poly(dA-dT)· poly(dA-dT) to the lac repressor of Escherichia coli.

Copurification of the Lac repressor with polyhistidine-tagged proteins in immobilized metal affinity chromatography.

One of the commonly used resins for immobilized metal affinity purification of polyhistidine-tagged recombinant proteins is TALON resin, a cobalt (II)--carboxymethylaspartate-based matrix linked to Sepharose CL-6B. Here, we show that TALON resin efficiently purifies the native form of Lac repressor, which represents the major contaminant when (His)(6)-tagged proteins are isolated from Escherichia coli host cells carrying the lacI(q) gene. Inspection of the crystal structure of the repressor suggests that three His residues (residues 163, 173, and 202) in each subunit of the tetramer are optimally spaced on an exposed face of the protein to allow interaction with Co(II). In addition to establishing a more efficient procedure for purification of the Lac repressor, these studies indicate that non-lacI(q)-based expression systems yield significantly purer preparations of recombinant polyhistidine-tagged proteins.

Manuel pratique d'identification des poissons du lac d'Ayamé (Rivière Bia, Côte d'Ivoire)

A taxonomic assessment of fish species was carried out in the Lake Ayamé as a preliminary evaluation within the framework of a project to appraise the biodiversity changes occurred in fish after the construction of a dam at Ayamé in 1959.

Étude comparative de la macrofaune associée aux racines de Pistia stratiotes L. (Araceae) du lac de barrage d'Ayamé II et du fleuve Comoé (Côte d'Ivoire)

Abundance and species variations of the macrofauna associated with the roots of Pistia stratiotes of Ayamé II lake and Comoé river were studied during one year. Samples of plants were collected by hand once a month within a sampler of 1 m2 of surface.

Developpement de la peche artisanale dans les eaux Burundaises du Lac Tanganyika

A light fishery for "Ndagala" (Strolothrissa tanganicae) has been practised for many years on Lake Tanganyika. Initially this had a low catch rate, but has since been developed by the introduction of an artisanal fishery unit based on the catamaran. A unit consists of a pair of metal canoes joined together. The fish are attracted by three lights mounted on the structure, and are caught with a pyramid-shaped lift net. Selected beaches have been reserved for the artisanal fishery and the numher of units operating has increased from 12 in 1957 to 538 in 1972. The mean annual catch per unit is 11,000 kg, which is not sufficient for the fishery to be economic. However, prediction of a possible mean catch as high as 40 tons year encouraged the Burundi Government to launch a project with help from the Freedom from Hunger Campaign. This was designed to develop the fishery by the creation of artisanal fishing centres, and to make available a large number of fully equipped catamarans which could be paid for by a system of hire-purchase. The success of the project has illustrated that the furnishing of adequate equipment can bring about a transformation of the traditional fishery.

表达lac和glk基因的蓝藻的异养生长

将来自Brucellaabortus的葡萄糖激酶基因glk和大肠杆菌乳糖操纵子基因lacZYA装置于蓝藻glnA启动子下游 ,以广宿主质粒导入 3种蓝藻。基因的表达通过 β 半乳糖苷酶和葡糖激酶活性测定得到确证。基因工程藻株均获得了利用乳糖异养生长的能力。集胞藻 6 80 3转基因株可在光照加DCMU的条件下利用乳糖生长 ,而鱼腥藻转基因株依赖乳糖可在完全黑暗条件下生长 ,并可在黑暗或加DCMU条件下诱导产生异形胞

Theoretical Investigation of LaC~n and La_2C~n(n=-1,0,+1)Clusters

用密度泛函方法研究了ＬａＣｎ及Ｌａ２Ｃｎ（ｎ＝－１，０，＋１）分子簇的结构和稳定性．对Ｌａ２Ｃｎ体系，提出了两种可能构型，其中一种具有Ｃ２ｖ对称性，另一种具有Ｄ∞ｈ对称性．计算结果表明，对Ｌａ２Ｃｎ，当ｎ＝＋１，－１时，线状结构最稳定，并且在ｎ＝＋１时，Ｃ２ｖ结构极不稳定有收敛向线状结构的趋势．而当ｎ＝０时，Ｃ２ｖ结构最稳定．最后还计算了ＬａＣ和Ｌａ２Ｃ分子簇的电子亲和势和离化能.

« Messire Lancelot du Lac » de « GAULTIER MOAP ». « Messire Lancelot du Lac » de « GAULTIER MOAP ».

Le f. 100 manque.

« Messire Lancelot du Lac » de « GAULTIER MOAP ». « Messire Lancelot du Lac » de « GAULTIER MOAP ».

Le f. 100 manque.

« Messire Lancelot du Lac » de « GAULTIER MOAP ». « Messire Lancelot du Lac » de « GAULTIER MOAP ».

Le f. 100 manque.