[en] The classic baculovirus expression system makes use of recombinant viruses to infect cells. This infection can, by the lytic activity of the virus, only result in transient expression of the recombinant protein. In this study, an alternative baculovirus expression system is demonstrated which is based on the property of viral immediate early genes, to be transcribed by uninfected cells in the absence of the other viral gene products. An immediate early gene of the baculovirus of Bombyx mori (BmNPVIEG) has been isolated and sequenced. By using an expression vector in which the lacZ reporter gene is placed under BmNPVIEG promoter control, expression of the lacZ reported gene in insect cells in a transient way was found. When the same expression vector was co-transfected with a construct containing the hygromycin B resistance gene, transformed Drosophila S2 cells were able to express the reporter gene continuously. (author). 8 refs

[en] With unprecedented advances in genetic engineering we are starting to see progressively more original examples of synthetic life. As such organisms become more common it is desirable to gain an ability to distinguish between natural and artificial life forms. In this paper, we address this challenge as a generalized version of Darwin’s original problem, which he so brilliantly described in On the Origin of Species . After formalizing the problem of determining the samples’ origin, we demonstrate that the problem is in fact unsolvable. In the general case, if computational resources of considered originator algorithms have not been limited and priors for such algorithms are known to be equal, both explanations are equality likely. Our results should attract attention of astrobiologists and scientists interested in developing a more complete theory of life, as well as of AI-Safety researchers. (invited comment)

[en] Gene transformation for the control of mosquito transmitted diseases is currently limited by the lack of an efficient method for the transfection and integration of exogenous DNA. The biolistic technique, which uses high velocity DNA coated microprojectiles, has been developed to introduce DNA into embryos of Anopheles gambiae. The biolistic parameters have been characterized and optimized on the basis of transient expression of the luciferase reporter gene placed under the control of the heat shock protein 70 promoter of Drosophila. High luciferase activities were observed for biolistic DNA introduction performed in the early embryonic stages. Because of the very large number of embryos which can easily be transfected biolistically, and because DNA is probably delivered directly into the nuclei, the biolistic method could be useful for obtaining insect genetic transformation, despite the low frequency of exogenous DNA integration. Moreover, this technique has already been proved suitable for embryo transfection in other invertebrates, such as crustaceans. (author). 8 refs

[en] Of environmental stresses, salinity has negative impacts on agricultural yield throughout the world; affected production is 1% as compared to 3%. Soil salinity affects plant growth and development by way of osmotic stress, injurious effects of toxic Na/sup +/ and Cl/sup -/ ions and to some extent Cl/sup -/ and SO/sub 4//sup 2-/ of Mg//sup 2+/. The plant response to salinity consists of numerous processes that must function in coordination to alleviate both cellular hyper osmolarity and ion disequilibrium. However, cell biology and molecular genetics research is providing new insight into the plant response to salinity and is identifying genetic determinants involved in the salt tolerance. Recent confirmation (Arabidopsis thaliana) to salt tolerance determinants is that mediate cellular ion homeostasis. The transport systems facilitate cellular capacity to utilize Na/sup +/ for osmotic adjustment and growth and the role of the Salt-Overly-Sensitive (SOS) signal transduction pathway in the regulation of ion homeostasis and salt tolerance. The SOS signaling pathway regulates Na/sup +/ and K/sup +/ homeostasis, after Ca/sup 2+/ activation. Furthermore, overexpression of AtNHX1 enhances plant salt tolerance, presumably by increasing vacuolar Na/sup +//H/sup +/ compartmentalization that minimizes the toxic I. accumulation of the ion in the cytosol. The activation of SOS1 (Na/sup +/ efflux) and/or AtNHX1 (Na/sup +/ efflux) so by expression of such transporters enhances salt tolerance in plants. (author)

[en] In synthetic biology, precise control over protein expression is required in order to construct functional biological systems. A core principle of the synthetic biology approach is a model-guided design and based on the biological understanding of the process, models of prokaryotic protein production have been described. Translation initiation rate is a rate-limiting step in protein production from mRNA and is dependent on the sequence of the 5′-untranslated region and the start of the coding sequence. Translation rate calculators are programs that estimate protein translation rates based on the sequence of these regions of an mRNA, and as protein expression is proportional to the rate of translation initiation, such calculators have been shown to give good approximations of protein expression levels. In this review, three currently available translation rate calculators developed for synthetic biology are considered, with limitations and possible future progress discussed.

No abstract available

[en] An ideal molecule to deliver radioimmunotherapy (RIT) would be target specific and have prolonged residence time at high concentrations in the tumour with rapid clearance from normal tissues. It would also be non-immunogenic. These features can be rationally introduced into recombinant antibody-based proteins using antibody engineering techniques. This reviews focuses on the use of antibody engineering in the design and development of RIT molecules which have single chain Fv (scFv) antibody fragments as building blocks

[en] Published in summary form only

[en] Manipulating living mammalian cells present fascinating possibilities for a plethora of applications within our healthcare. These imply several possibilities in tissue engineering and regenerative medicine, to those of a therapeutic nature. The physical sciences are increasingly playing a pivotal role in this endeavour by both advancing existing cell engineering technology and pioneering new protocols for the creation of biologically viable structures. In this paper, the author introduces several direct needle/channel/orifice-based cell engineering protocols, currently undergoing intense investigation for a whole host of bio-applications. Hence, each protocol's advantages and disadvantages are clearly identified, whilst recognizing their future biological and engineering challenges. In conclusion, a few selected biotechnological applications present possibilities where these protocols could undergo focused exploration. Successful development of these bio-protocols sees the emergence of unique future strategies within a clinical environment having far-reaching consequences for our healthcare

[en] A dengue-1 DNA vaccine containing sequences encoding premembrane and envelope proteins (DIME) was previously shown to elicit virus neutralizing antibodies in rhesus and Aotus monkeys, and the primates were partially protected from viremia upon challenge. To increase the neutralizing antibody levels and subsequent protection from virus challenge, four strategies were evaluated: (a) coimmunization with a plasmid expressing Aotus GM-CSF gene; (b) coimmunization with a plasmid containing human immunostimulatory sequences (ISS); (c) coimmunization with both the GM-CSF gene and ISS; and (d) delivery of vaccine using the needle-free Biojector system. Vaccination with the mixed formulation containing DIME, GM-CSF gene, and ISS, by either needle injection or Biojector, led to neutralizing antibody titers that were stable for up to 6 months after vaccination. Furthermore, 6 of 7 monkeys (85%), and 7 of 8 monkeys (87%) receiving this formulation were completely protected from viremia when challenged 1 and 6 months after vaccination, respectively. This is a significant improvement compared to our previous study in which one of three monkeys (33%) receiving just the DIME vaccine was completely protected from viremia at 6 months after immunization