Modelling the kinetics of thermal inactivation of apple polyphenoloxidase

The enzymatic browning of fruits and vegetables caused by mechanical injury during postharvest storage or processing is initiated by the catalytic action of polyphenoloxidase (PPO). A bleaching treatment prior to processing is still considered mostly effective in inhibiting the catalytic activity of PPO, and thus controlling undesirable enzymatic browning. In this work, different mathematical routines were assessed in terms of their adequacy to describe the thermal inactivation of PPO from Golden apples over a range of temperatures from 62.5 to 72.5 ºC. The classical approach to kinetic modelling of the decay activity of apple PPO, commonly reported to follow a first-order model, employs a two-step procedure, in which the model parameters are individually obtained, by each temperature studied, using non-linear or linear regressions. Thereafter, the estimated parameters are further used to calculate their temperature dependence. Alternatively, a one-step method provides a regression fit to all experimental data sets, with the temperature dependence equation being directly built in the kinetic model. This fitting technique thus, (a) avoids the estimation of intermediate parameters and, (b) substantially increases the degrees of freedom and hence the precision of parameters’ estimates. Within this issue was further explored the logarithmic transformation of the mathematical equations used on the adequacy of the model to describe experimental data. In all cases non-weighted least-squares regression procedures were used. Both the examination and criticism of the current modelling strategies were done by assessing statistical data obtained, such as the confidence intervals of the estimates, correlation coefficients, sum of squares, and residuals normality

Quasi-Dirac neutrinos and solar neutrino data

We present an analysis of the solar neutrino data in the context of a quasi-Dirac neutrino model in which the lepton mixing matrix is given at tree level by the tribimaximal matrix. When radiative corrections are taken into account, new effects in neutrino oscillations, as $\nu_e \to \nu_s$, appear. This oscillation is constrained by the solar neutrino data. In our analysis, we have found an allowed region for our two free parameters $\epsilon$ and $m_1$. The radiative correction, $\epsilon$, can vary approximately from $5\times 10^{-9}$ to $10^{-6}$ and the calculated fourth mass eigenstate, $m_4$, 0.01 eV to 0.2 eV at 2$\sigma$ level. These results are very similar to the ones presented in the literature.Comment: 24 pages, 7 figures and 2 tables. Results and conclusion unchanged. Version published in EPJC. Figures improve

Experimental joint immobilization in guinea pigs. Effects on the knee joint

In young and adult guinea pigs, the aftermath experimentally induced by the immobilization of the knee joint in hyperextended forced position was studied. Joint immobilization which varied from one to nine weeks was attained by plaster. Eighty knee joints were examined macro and microscopically. Findings included: (1) muscular hypotrophy and joint stiffness in all animals, directly proportional to the length of immobilization; (2) haemoarthrosis in the first week; (3) intra-articular fibrous tissue proliferation ending up with fibrous ankylosis; (4) hyaline articular cartilage erosions; (5) various degrees of destructive menisci changes. A tentative explanation of the fibrous tissue proliferation and of the cartilage changes is offered

Cytoskeletal turnover and Myosin contractility drive cell autonomous oscillations in a model of Drosophila Dorsal Closure

Oscillatory behaviour in force-generating systems is a pervasive phenomenon in cell biology. In this work, we investigate how oscillations in the actomyosin cytoskeleton drive cell shape changes during the process of Dorsal Closure, a morphogenetic event in Drosophila embryo development whereby epidermal continuity is generated through the pulsatile apical area reduction of cells constituting the amnioserosa (AS) tissue. We present a theoretical model of AS cell dynamics by which the oscillatory behaviour arises due to a coupling between active Myosin-driven forces, actin turnover and cell deformation. Oscillations in our model are cell-autonomous and are modulated by neighbour coupling, and our model accurately reproduces the oscillatory dynamics of AS cells and their amplitude and frequency evolution. A key prediction arising from our model is that the rate of actin turnover and Myosin contractile force must increase during DC in order to reproduce the decrease in amplitude and period of cell area oscillations observed in vivo. This prediction opens up new ways to think about the molecular underpinnings of AS cell oscillations and their link to net tissue contraction and suggests the form of future experimental measurements.Comment: 17 pages, 6 figures; added references, modified and corrected Figs. 1 and 3, corrected typos, expanded discussio