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Wise, L.

Publications and source records attributed to Wise, L..

3 recordsLinked to original sources

Thermodynamic Constraints on Electromicrobial Protein Production

Global consumption of protein is projected to double by the middle of the 21st century1. However, protein production is one of the most energy intensive and environmentally damaging parts of the food supply system today. Electromicrobial production technologies that combine renewable electricity and CO2-fixing microbial metabolism could dramatically increase the energy efficiency of commodity chemical production2-5. Here we present a molecular-scale model that sets an upper limit on the performance of any organism performing electromicrobial protein production. We show that engineered microbes that fix CO2 and N2 using reducing equivalents produced by H2-oxidation or extracellular electron uptake could produce amino acids with energy inputs as low as 64 MJ kg-1. This work provides a roadmap for development of engineered microbes that could significantly expand access to proteins produced with a low environmental footprint.

synthetic biology↗

Concurrent Multimodal Data Acquisition During Brain Scanning is within Reach

BackgroundPrevious brain-scanning research exploring the neural mechanisms underpinning visuomotor planning and control has mostly been done without simultaneous motion-tracking and eye-tracking. Employing concurrent methodologies would enhance understanding of the brain mechanisms underlying visuomotor integration of cognitive, visual, ocular, and motor aspects of reaching and grasping behaviours. Therefore, this work presents the methods and validation for a high-speed, multimodal and synchronized system to holistically examine neural processes that are involved in visually-guided movement. MethodsThe multimodal methods included high speed 3D motion tracking (Qualisys), 2D eye-tracking (SR Research), and magnetoencephalography (MEG; Elekta) that were synchronized to millisecond precision. Previous MRIs were taken to provide improved spatial localization. The methods section describes the system layout and acquisition parameters to achieve multimodal synchronization. Pilot results presented here are preliminary data from a larger study including 29 participants. Using a pincer grip, five people (3 male, 2 female, ages 30-32) reached for and grasped a translucent dowel 50 times, after it was pseudorandomly illuminated. The object illumination was the Go cue. Seven discrete time points (events) throughout the task were chosen for investigation of simultaneous brain, hand and eye activity associated with specific visual (Go cue), oculomotor (1st saccade after Go), motor (Reaction Time; RT, Maximum Velocity: MV, Maximum Grip Width; MGW) or cognitive (Ready, End) mechanisms. Time-frequency analyses were performed on the MEG data sourced from the left precentral gyrus to explore task-related changes time-locked to these chosen events. Pilot resultsBasic kinematic parameters including RT, MV, MGW, Movement Time, and Total Time were similar to previous, seminal research by Castiello, Paulignan and Jeannerod, (1991), using a similar task. Although no gaze instructions were given, eye-tracking results indicated volunteers mostly gazed at or near the target object when Ready (72%), and then hardly looked away throughout the rest of the task at the important events sampled here (92% - 98%). At the End event, when lifting the dowel, on average, participants gazed at or near the target object 100% of the time. Although saccades > 100 ms after Go, but prior to RT were made on average in about one fourth (M = 13, SD = 6) of trials, a mixed model (REML) indicated their latency in timing after the Go was significantly (F = 13.376, p = .001) associated with RT scores on those trials (AIC = 724, R m2 = 0.407, Rc2= 0.420). Neural activity relative to baseline in the beta band was desynchronized for the visually guided reach periods, beginning prior to Go, and remaining sustained until beyond End, after the grasp and lift were executed. ConclusionThis study presents the layout, acquisition parameters and validation for a multimodal, synchronized system designed to record data from the hand, eye and brain simultaneously, with millisecond precision during an ecologically-valid prehension task with physical, 3D objects. The pilot results align with previous research made with single or bimodal data recordings. This multimodal method enables full-brain modelling that can holistically map the precise location and timing of neural activity involved in the visual, oculomotor, motor and cognitive aspects of reach-to-grasp planning and control.

neuroscience↗

Human Cytomegalovirus Remodeling of Lipid Metabolism Requires pUL37x1

Human cytomegalovirus (HCMV) replication requires remodeling of the host metabolic network, including increasing central carbon metabolism, fatty acid elongation and lipid synthesis. The virus-host interactions regulating HCMV metabolic hijacking are essential to infection. While multiple host factors including kinases and transcription factors have been defined, little is known about the viral factors required. Some host factors involved are dependent on Ca2+ signaling or host stress response. The viral pUL37x1 protein mobilizes Ca2+ and targets the mitochondria. The Ca2+ changes induced by pUL37x1 can activate stress responses. In this study, we tested the hypothesis that the viral pUL37x1 protein is required for HCMV metabolic remodeling. Using a combination of metabolomics, lipidomics, and metabolic tracers, we demonstrate that pUL37x1 protein is necessary for HCMV induced fatty acid elongation and lipid metabolism but not required for most viral hijacking of central carbon metabolism. Additionally, we show that pUL37x1 is required for HCMV to fully induce two host proteins that were previously demonstrated to be important for virus induced lipid metabolism: fatty acid elongase 7 and the ER-stress related kinase PERK. We also demonstrate, for the first time, that HCMV replication results in the increase in phospholipids with very-long chain fatty acyl tails. We conclude that pUL37x1 is required for HCMV metabolic remodeling but is not necessary to for the virus to hijack metabolism on a network-wide scale.

microbiology↗