Antineutrino Physics at MINOS

We present two new measurements of antineutrino properties based on a data sample corresponding to 3.2×10^(20) protons-on-target, exploiting MINOS' unique ability to distinguish positive and negative muons and thus separate charged current neutrino and antineutrino interactions event-by-event. The first measurement takes advantage of the 6% antineutrino component of the NuMI neutrino beam to measure antineutrino oscillations between the near and far detectors. We observe 42 events at the far detector with an expectation of 58.3±7.6(stat.)±3.6(syst.) assuming CPT-conserving oscillations, excluding (5.0<Δm(overbar)^2<81)×10^(−3)eV^2 at 90% confidence at maximal mixing. We also present a search for neutrino-antineutrino transitions ν_μ → ν(overbar)_μ, which would result in an excess of antineutrino events in the Far Detector relative to the rate expected from the intrinsic antineutrino component in the neutrino beam. We observe no excess and set a limit of 0.026 on the transition probability at 90% confidence

Search for Lorentz Invariance and CPT Violation with the MINOS Far Detector

We searched for a sidereal modulation in the MINOS far detector neutrino rate. Such a signal would be a consequence of Lorentz and CPT violation as described by the standard-model extension framework. It also would be the first detection of a perturbative effect to conventional neutrino mass oscillations. We found no evidence for this sidereal signature, and the upper limits placed on the magnitudes of the Lorentz and CPT violating coefficients describing the theory are an improvement by factors of 20–510 over the current best limits found by using the MINOS near detector

Improved Measurement of Muon Antineutrino Disappearance in MINOS

We report an improved measurement of ν̅_μ disappearance over a distance of 735 km using the MINOS detectors and the Fermilab Main Injector neutrino beam in a ν̅_μ-enhanced configuration. From a total exposure of 2.95×10^20 protons on target, of which 42% have not been previously analyzed, we make the most precise measurement of Δm̅^2=[2.62_(-0.28)^(+0.31)(stat)±0.09(syst)]×10^(-3)  eV^2 and constrain the ν_μ mixing angle sin^(2)(2θ̅)>0.75 (90% C.L.). These values are in agreement with Δm^2 and sin^(2)(2θ) measured for νμ, removing the tension reported in [ P. Adamson et al. Phys. Rev. Lett. 107 021801 (2011)]

Glycosylation of hyperthermostable designer cellulosome components yields enhanced stability and cellulose hydrolysis

Biomass deconstruction remains integral for enabling second‐generation biofuel production at scale. However, several steps necessary to achieve significant solubilization of biomass, notably harsh pretreatment conditions, impose economic barriers to commercialization. By employing hyperthermostable cellulase machinery, biomass deconstruction can be made more efficient, leading to milder pretreatment conditions and ultimately lower production costs. The hyperthermophilic bacterium Caldicellulosiruptor bescii produces extremely active hyperthermostable cellulases, including the hyperactive multifunctional cellulase CbCel9A/Cel48A. Recombinant CbCel9A/Cel48A components have been previously produced in Escherichia coli and integrated into synthetic hyperthermophilic designer cellulosome complexes. Since then, glycosylation has been shown to be vital for the high activity and stability of CbCel9A/Cel48A. Here, we studied the impact of glycosylation on a hyperthermostable designer cellulosome system in which two of the cellulosomal components, the scaffoldin and the GH9 domain of CbCel9A/Cel48A, were glycosylated as a consequence of employing Ca. bescii as an expression host. Inclusion of the glycosylated components yielded an active cellulosome system that exhibited long‐term stability at 75 °C. The resulting glycosylated designer cellulosomes showed significantly greater synergistic activity compared to the enzymatic components alone, as well as higher thermostability than the analogous nonglycosylated designer cellulosomes. These results indicate that glycosylation can be used as an essential engineering tool to improve the properties of designer cellulosomes. Additionally, Ca. bescii was shown to be an attractive candidate for production of glycosylated designer cellulosome components, which may further promote the viability of this bacterium both as a cellulase expression host and as a potential consolidated bioprocessing platform organism

Cellulose crystallinity index: measurement techniques and their impact on interpreting cellulase performance

Although measurements of crystallinity index (CI) have a long history, it has been found that CI varies significantly depending on the choice of measurement method. In this study, four different techniques incorporating X-ray diffraction and solid-state 13C nuclear magnetic resonance (NMR) were compared using eight different cellulose preparations. We found that the simplest method, which is also the most widely used, and which involves measurement of just two heights in the X-ray diffractogram, produced significantly higher crystallinity values than did the other methods. Data in the literature for the cellulose preparation used (Avicel PH-101) support this observation. We believe that the alternative X-ray diffraction (XRD) and NMR methods presented here, which consider the contributions from amorphous and crystalline cellulose to the entire XRD and NMR spectra, provide a more accurate measure of the crystallinity of cellulose. Although celluloses having a high amorphous content are usually more easily digested by enzymes, it is unclear, based on studies published in the literature, whether CI actually provides a clear indication of the digestibility of a cellulose sample. Cellulose accessibility should be affected by crystallinity, but is also likely to be affected by several other parameters, such as lignin/hemicellulose contents and distribution, porosity, and particle size. Given the methodological dependency of cellulose CI values and the complex nature of cellulase interactions with amorphous and crystalline celluloses, we caution against trying to correlate relatively small changes in CI with changes in cellulose digestibility. In addition, the prediction of cellulase performance based on low levels of cellulose conversion may not include sufficient digestion of the crystalline component to be meaningful