Characterization and expression analysis of a serine acetyltransferase gene family involved in a key step of the sulfur assimilation pathway in Arabidopsis

Ser acetyltransferase (SATase; EC 2.3.1.30) catalyzes the formation of O-acetyl-Ser from L-Ser and acetyl-CoA, leading to synthesis of Cys. According to its position at the decisive junction of the pathways of sulfur assimilation and amino acid metabolism, SATases are subject to regulatory mechanisms to control the flux of Cys synthesis. In Arabidopsis (Arabidopsis thaliana) there are five genes encoding SATase-like proteins. Two isoforms, Serat3;1 and Serat3;2, were characterized with respect to their enzymatic properties, feedback inhibition by L-Cys, and subcellular localization. Functional identity of Serat3;1 and Serat3;2 was established by complementation of a SATase-deficient mutant of Escherichia coli. Cytosolic localization of Serat3;1 and Serat3;2 was confirmed by using fusion construct with the green fluorescent protein. Recombinant Serat3;1 was not inhibited by L-Cys, while Serat3;2 was a strongly feedback-inhibited isoform. Quantification of expression patterns indicated that Serat2;1 is the dominant form expressed in most tissues examined, followed by Serat1;1 and Serat2;2. Although Serat3;1 and Serat3;2 were expressed weakly in most tissues, Serat3;2 expression was significantly induced under sulfur deficiency and cadmium stress as well as during generative developmental stages, implying that Serat3;1 and Serat3;2 have specific roles when plants are subjected to distinct conditions. Transgenic Arabidopsis plants expressing the green fluorescent protein under the control of the five promoters indicated that, in all Serat genes, the expression was predominantly localized in the vascular system, notably in the phloem. These results demonstrate that Arabidopsis employs a complex array of compartment-specific SATase isoforms with distinct enzymatic properties and expression patterns to ensure the provision of Cys in response to developmental and environmental changes.     

Rapid and stable production of 2,3-butanediol by an engineered <Emphasis Type="Italic">Saccharomyces cerevisiae</Emphasis> strain in a continuous airlift bioreactor

Utilization of renewable feedstocks for the production of bio-based bulk chemicals, such as 2,3-butanediol (2,3-BDO), by engineered strains of the non-pathogenic yeast, Saccharomyces cerevisiae, has recently become an attractive option. In this study, to realize rapid production of 2,3-BDO, a flocculent, 2,3-BDO-producing S. cerevisiae strain YPH499/dPdAdG/BDN6-10/FLO1 was constructed from a previously developed 2,3-BDO-producing strain. Continuous 2,3-BDO fermentation was carried out by the flocculent strain in an airlift bioreactor. The strain consumed more than 90 g/L of glucose, which corresponded to 90% of the input, and stably produced more than 30 g/L of 2,3-BDO over 380 h. The maximum 2,3-BDO productivity was 7.64 g/L/h at a dilution rate of 0.200/h, which was higher than the values achieved by continuous fermentation using pathogenic bacteria in the previous reports. These results demonstrate that continuous 2,3-BDO fermentation with flocculent 2,3-BDO-producing S. cerevisiae is a promising strategy for practical 2,3-BDO production.     

Morphological,distributional, and genetic characteristics of <Emphasis Type="Italic">Cottus pollux</Emphasis> in the Kyushu Island,Japan: indication of fluvial and amphidromous life histories within a single lineage

We evaluated the morphological, distributional, and genetic characteristics of the freshwater sculpin, Cottus pollux, in Kyushu Island, Japan. Based on pectoral fin ray number, the sculpins inhabiting 30 rivers were divided into two types [modes 13 (M13) and 15 (M15)]. We evaluated four environmental parameters: length of main river (L-MR), average gradient of main river (G-MR), distance from sampling site to river mouth (D-SM), and gradient around sampling site (G-S), and compared the two types. L-MR, D-SM, and G-S were significantly larger for the rivers that contained M13 fish than for those containing M15 fish. M13 individuals were distributed in the upstream areas of large river systems, suggesting a fluvial life history, whereas M15 individuals were distributed in the downstream areas of small river systems, indicating an amphidromous life history. We conducted phylogenetic analysis based on mitochondrial 12S rRNA [788 base pair (bp)] and control regions (386 bp). Mitochondrial DNA analysis showed that both M13 and M15 groups were genetically of C. pollux middle-egg type (ME). Our findings proposed the hypothesis that C. pollux ME in Kyushu Island exhibits dimorphism in both morphological and distributional traits. Additionally, haplotype distribution indicated that the fluvial M13 populations had higher genetic specificity in each river in contrast to the existence of one genetic group of amphidromous M15 individuals in Kyushu Island.     

Characterization of the Roles of the Saccharomyces Cerevisiae Rad54 Gene and a Homologue of Rad54, Rdh54/Tid1, in Mitosis and Meiosis

The RAD54 gene, which encodes a protein in the SWI2/SNF2 family, plays an important role in recombination and DNA repair in Saccharomyces cerevisiae. The yeast genome project revealed a homologue of RAD54, RDH54/TID1. Properties of the rdh54/tid1 mutant and the rad54 rdh54/tid1 double mutant are shown for mitosis and meiosis. The rad54 mutant is sensitive to the alkylating agent, methyl methanesulfonate (MMS), and is defective in interchromosomal and intrachromosomal gene conversion. The rdh54/tid1 single mutant, on the other hand, does not show any significant deficiency in mitosis. However, the rad54 rdh54/tid1 mutant is more sensitive to MMS and more defective in interchromosomal gene conversion than is the rad54 mutant, but shows the same frequency of intrachromosomal gene conversion as the rad54 mutant. These results suggest that RDH54/TID1 is involved in a minor pathway of mitotic recombination in the absence of RAD54. In meiosis, both single mutants produce viable spores at slightly reduced frequency. However, only the rdh54/tid1 mutant, but not the rad54 mutant, shows significant defects in recombination: retardation of the repair of meiosis-specific double-strand breaks (DSBs) and delayed formation of physical recombinants. Furthermore, the rad54 rdh54/tid1 double mutant is completely defective in meiosis, accumulating DSBs with more recessed ends than the wild type and producing fewer physical recombinants than the wild type. These results suggest that one of the differences between the late stages of mitotic recombination and meiotic recombination might be specified by differential dependency on the Rad54 and Rdh54/Tid1 proteins.     

Structure and subcellular localization of a small RNA-binding protein from tobacco

In this study, a cDNA encoding a small RNA-binding protein was isolated from a Nicotiana sylvestris cDNA library. The predicted protein (RGP-3) is 144 amino acid residues long, and contains a consensus sequence-type RNA binding domain (CS-RBD) of 83 amino acids and a short glycine-rich region of 15 amino acids. RGP-3 synthesized in Escherichia coli has high affinity for poly(U). Immunocytochemical analysis indicated that RGP-3 is localized in the nucleoplasm, and that RGP-1b, a related protein reported previously, is localized in the nucleolus. Possible roles of these proteins in pre-mRNA or pre-rRNA processing are discussed.     

Growth stimulation with honey royal jelly DIII protein of human lymphocytic cell lines in a serum-free medium

Summary The growth stimulating effects of a royal jelly protein (DIII protein) were studied. The DIII protein stimulated the growth of five human lymphocytic cell lines in serum-free conditions. Cell cycle analysis showed that U-937 cells cultured with the DIII protein did not arrest to the G1 phase. Furthermore, a binding assay using europium-labeled DIII protein showed U-937 cells had a large number of low affinity receptors on the cell surface.     

Experimental Investigation of the Mechanism of Reproductive Differentiation in the Queenless Ant,Diacamma sp., from Japan

We test two hypotheses about regulation of the reproductive division of labour in the permanently queenless ponerine ant, Diacamma sp., from Japan. All workers emerge with gemmae (tiny innervated thoracic appendages), but only one individual keeps them in each colony, and she is the only mated reproductive worker (gamergate). The gemmae of all other workers are mutilated by the gamergate soon after their emergence, and they can never mate. In the presence of gamergate, mutilated workers have inactive ovaries and do not behave aggressively. Two possible consequences of mutilation are: 1. olfactory signal — a pheromone inhibiting the oogenesis of mutilated workers is no longer released by the gemmae; and 2. endocrine degeneration of its afferent neuronal connections interferes reproductive physiology of a gamergate. Gemmae of gamergates were coated with shellac (to prevent pheromone emission) or removed, and over three weeks we studied any changes in ovarian activity of the gamergates as well as nestmate workers. Coating of gemmae did not elicit worker oviposition, suggesting that gemmae pheromones do not have a regulatory function. Experimental mutilation of gamergates resulted in a slight increase in both the frequency of dominance interactions and the ovarian activity of mutilated workers, but this effect was much lower than in colonies where the gamergate was removed. This contrasts with the immediate change in the behaviour (aggressive to timid) of newly emerged workers following mutilation.