No abstract

The use of remote laboratories for education is increasing because it is a method that allows a better use of resources (laboratories operate 24 hours a day) and students interact with real equipment from different locations. However, we can say that there are as many particular solutions as remote labs can be found today. In this paper, we present a design framework for remote laboratories, covering the various aspects involved and completely based on free software. Within this approach, professors have all the tools required to convert a laboratory experiment in a remote experiment. Moreover, they can also design an user interface that includes augmented reality techniques to enrich the user experience.

Remote labs are emerging as a necessary tool to support practical classes in engineering studies. It is due to the increasing number of students who combine their studies with work. In fact, there are numerous developments in areas such as electronics and automatic. However, there are only a few of them in the area of electrical machines. This paper presents a testing bench for remote practical training in electric machines. The security challenges presented by these experiments are overcome by software within the remote lab. In addition, a friendly interface has been designed including augmented reality to identify the different elements and to provide information on these items if the student requires it. The testing bench has been developed to be used in different kinds of electrical machines test.

Genetic manipulation shows great promise to further boost the productivity of microalgae-based compounds. However, selection of microalgal transformants depends mainly on the use of antibiotics, which have raised concerns about their potential impacts on human health and the environment. We propose the use of a synthetic phytoene desaturase-encoding gene (CRTIop) as a selectable marker and the bleaching herbicide norflurazon as a selective agent for the genetic transformation of microalgae. Bacterial phytoene desaturase (CRTI), which, unlike plant and algae phytoene desaturase (PDS), is not sensitive to norflurazon, catalyzes the conversion of the colorless carotenoid phytoene into lycopene. Although the expression of CRTI has been described to increase the carotenoid content in plant cells, its use as a selectable marker has never been testedin algae or in plants. In this study, a version of the CRTI gene adapted to the codon usage of Chlamydomonas has been synthesized, and its suitability to be used as selectable marker has been shown. The microalgae were transformed by the glass bead agitation method and selected in the presence of norflurazon. Average transformation efficiencies of 550 colonies µg−1 DNA were obtained. All the transformants tested had incorporated the CRTIop gene in their genomes and were able to synthesize colored carotenoids.