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Experimental and System-Level Simulation Study of Stick-Slip Characteristics in Pneumatic Cylinders
Hai Nguyen Ngoc
,Phu Phung Pham
,Bo Tran Xuan
Posted: 02 April 2026
On the Cross-Scale Prospects of the Logarithmically Corrected Gravitational Potential: From Black Hole Singularities to Galactic Rotation
Huang Hai
Posted: 02 April 2026
A Measure-Theoretic Formulation of Monte Carlo Stochastic Optimization: Unifying Continuous and Discrete Domains
Shin-Ichi Inage
Posted: 02 April 2026
Expression and Partial Characterization of Alkaline Pectate Lyase A from Paenibacillus barcinonensis in a Glycosylation-Deficient Strain of Saccharomyces cerevisiae
Expression and Partial Characterization of Alkaline Pectate Lyase A from Paenibacillus barcinonensis in a Glycosylation-Deficient Strain of Saccharomyces cerevisiae
María Mormeneo
,Ismaïl Moukadiri
,Jesús Zueco
The alkaline pectate lyase A from Paenibacillus barcinonensis, encoded by pelA (GenBank accession no. CAB40884), is an enzyme with high activity on pectin and potential application in sustainable industrial biotechnology. In this study, pelA was expressed in Saccharomyces cerevisiae by using different domains of the cell wall protein Pir4 as translational fusion partners. Given the presence of five potential N-glycosylation sites in the amino acid sequence coded by pelA, two of them in conserved regions of class III pectate lyases, the effect of glycosylation on the enzymatic activity of the recombinant enzyme was investigated by expressing the recombinant fusion proteins in both, standard and glycosylation deficient strains of S. cerevisiae. Correct targeting of the recombinant fusion proteins was confirmed by Western blot analysis using Pir-specific antibodies, whilst enzymatic activity on polygalacturonic acid was demonstrated on both plate assays and colorimetric assays. Hyper- glycosylation of the enzyme when expressed in the standard strain of S. cerevisiae did not occur, however maximum activities were over two and a half times higher when the enzyme was expressed in the glycosylation deficient strain, suggesting a better adaptation of this strain to the secretion of the functional enzyme. Notably, pectate lyase activity was approximately fourfold higher when the pelA gene was expressed in this yeast strain compared to its expression in a prokaryotic host such as Bacillus subtilis or Escherichia coli.
The alkaline pectate lyase A from Paenibacillus barcinonensis, encoded by pelA (GenBank accession no. CAB40884), is an enzyme with high activity on pectin and potential application in sustainable industrial biotechnology. In this study, pelA was expressed in Saccharomyces cerevisiae by using different domains of the cell wall protein Pir4 as translational fusion partners. Given the presence of five potential N-glycosylation sites in the amino acid sequence coded by pelA, two of them in conserved regions of class III pectate lyases, the effect of glycosylation on the enzymatic activity of the recombinant enzyme was investigated by expressing the recombinant fusion proteins in both, standard and glycosylation deficient strains of S. cerevisiae. Correct targeting of the recombinant fusion proteins was confirmed by Western blot analysis using Pir-specific antibodies, whilst enzymatic activity on polygalacturonic acid was demonstrated on both plate assays and colorimetric assays. Hyper- glycosylation of the enzyme when expressed in the standard strain of S. cerevisiae did not occur, however maximum activities were over two and a half times higher when the enzyme was expressed in the glycosylation deficient strain, suggesting a better adaptation of this strain to the secretion of the functional enzyme. Notably, pectate lyase activity was approximately fourfold higher when the pelA gene was expressed in this yeast strain compared to its expression in a prokaryotic host such as Bacillus subtilis or Escherichia coli.
Posted: 02 April 2026
Edge AI Phenomics Tracking Motor Proficiency and Psychosocial Benefits in Sensory- Impaired Children’s Recreational Programs
A. Manoj Prabaharan
Posted: 02 April 2026
In Vitro Inhibition of Pathogens by Polyols: Optical Density-Based Screening and Implications for the Oral-Systemic Axis
Mark Cannon
,Bradley S. Stevenson
Polyols are widely used as non-cariogenic sweeteners in foods and oral care products, yet their comparative activity against diverse oral microbes and their potential relevance to the oral–systemic axis remain incompletely defined. Here, we performed an in vitro, optical-density (OD)-based screening of four polyols—allulose, D-mannose, erythritol, and xylitol—against Streptococcus mutans, Streptococcus anginosus, Candida albicans, and Fusobacterium nucleatum. Cultures were grown with polyols at 1–20% (w/v), and OD600 was recorded at organism-specific endpoints (~24 h). Allulose, erythritol, and xylitol produced strong, concentration-dependent suppression of streptococcal growth at ≥5–10%, whereas C. albicans showed minimal changes across the tested range. F. nucleatum was highly sensitive to allulose, D-mannose, and xylitol at ≥5% (reducing OD to ≤13% of untreated control), while low concentrations of D-mannose and erythritol increased OD above control, suggesting species-specific utilization or stress responses. One-way ANOVA with Tukey’s HSD post hoc testing supported significant between-polyol differences for most concentrations in Streptococcus spp. and F. nucleatum. Collectively, these results identify polyol- and taxon-specific growth phenotypes that can inform the formulation of swallow-safe oral hygiene products and motivate follow-up work in polymicrobial biofilm models and clinical studies targeting oral inflammation and downstream systemic risk.
Polyols are widely used as non-cariogenic sweeteners in foods and oral care products, yet their comparative activity against diverse oral microbes and their potential relevance to the oral–systemic axis remain incompletely defined. Here, we performed an in vitro, optical-density (OD)-based screening of four polyols—allulose, D-mannose, erythritol, and xylitol—against Streptococcus mutans, Streptococcus anginosus, Candida albicans, and Fusobacterium nucleatum. Cultures were grown with polyols at 1–20% (w/v), and OD600 was recorded at organism-specific endpoints (~24 h). Allulose, erythritol, and xylitol produced strong, concentration-dependent suppression of streptococcal growth at ≥5–10%, whereas C. albicans showed minimal changes across the tested range. F. nucleatum was highly sensitive to allulose, D-mannose, and xylitol at ≥5% (reducing OD to ≤13% of untreated control), while low concentrations of D-mannose and erythritol increased OD above control, suggesting species-specific utilization or stress responses. One-way ANOVA with Tukey’s HSD post hoc testing supported significant between-polyol differences for most concentrations in Streptococcus spp. and F. nucleatum. Collectively, these results identify polyol- and taxon-specific growth phenotypes that can inform the formulation of swallow-safe oral hygiene products and motivate follow-up work in polymicrobial biofilm models and clinical studies targeting oral inflammation and downstream systemic risk.
Posted: 02 April 2026
Active Vision for Social Navigation
Jack Vice
,Gita Sukthankar
Posted: 02 April 2026
Impact of a Single Hemodialysis Session on Oxidative Stress-Inducing and Oxidative Damage Biomarkers in End-Stage Kidney Disease Patients
Athina Varemmenou
,Effimia Michail
,Electra Kalaitzopoulou
,Polyxeni Papadea
,Marianna Skipitari
,Marios Papasotiriou
,Evangelos Papachristou
,Dimitrios Goumenos
,Christos D. Georgiou
Posted: 02 April 2026
Hormonal and Emerging Therapeutic Strategies in Endometriosis: Translating Pathophysiology into Targeted Treatment
Sara Perelmuter
Posted: 02 April 2026
Alzheimer’s Disease, Piezo2 Channelopathy, Piezo1 Channelopathy and the Body-Wide Piezo2 System
Balazs Sonkodi
Posted: 02 April 2026
Beyond Random Splits: A Critical Evaluation of Graph Learning Models in Predicting Mutation-Induced Drug Resistance
Zongrui Cheng
,Haoxin Wu
,Dengming Ming
Posted: 02 April 2026
Lipid Nanoparticle-Encapsulated PolyI:C as an Adjuvant Enhances Both Humoral and Cellular Immune Responses to the Hepatitis B Vaccine
Zhixian Zhao
,Bin Wang
,Hao Wang
,Qiang Zhang
,Yunfei Liang
,Yuan Liu
Posted: 02 April 2026
Optimizing Multi-Scalar Multiplication Over Fixed Bases
Saulius Grigaitis
Posted: 02 April 2026
Helium Free MRI System—What Does That Mean for a Decision Maker?
Michael Friebe
Posted: 02 April 2026
Influence of Both La Nina and Island Isolation During COVID-19 on the Epidemiology of Infectious Diseases in New-Caledonia
Pierre-Henri Moury
,Ann-Claire Gourinat
,Maria Suveges
,Méryl Delrieu
,Myrielle Dupont-Rouzeyrol
,Christophe Menkes
,Nathanaëlle Soler
,Cécile Cazorla
,Antoine Biron
,Antoine Flahault
+2 authors
Posted: 02 April 2026
The Effect of Caffeine on Various Forms of Synaptic Plasticity in the CA1 Region of Mouse Hippocampal Slices
Margarita A. Novikova
,Irina A. Korneeva
,Rodion V. Kondratenko
,Georgii M. Nikolaev
,Olga A. Averina
,Irina N. Sharonova
,Alexander V. Latanov
Posted: 02 April 2026
Neuronal Ceroid Lipofuscinosis-Like Disorder in a Dachshund with Sequence Variants in Lysosome-Related Genes
Joan R. Coates
,Kristen Keyes
,Rebecca E.H. Whiting
,Juri Kuroki
,Brandie Morgan-Jack
,Tendai Mhlanga-Mutangadura
,Keiichi Kuroki
,Martin L. Katz
Posted: 02 April 2026
Functional Integration of a Portable Non-Enzymatic Electrochemical Glucose Sensor in Simulation-Based Medical Education Through a Teleconsultation Workflow
Leonel Vasquez-Cevallos
,Darwin Castillo
,Pedro A. Salazar-Carballo
,Paul E.D. Soto-Rodriguez
,Franklin Parrales-Bravo
,Roberto Tolozano-Benites
Posted: 02 April 2026
A Grammar-Based Criterion for Learning Sufficiency in Motion Modeling
Herlindo Hernandez-Ramirez
,Jorge Luis Perez-Ramos
,Daniel Canton-Enriquez
,Ana Marcela Herrera-Navarro
,Hugo Jimenez-Hernandez
Posted: 02 April 2026
The Theory of Plafales: P vs NP Problem Solution
Dmytro Topchyi
Posted: 02 April 2026
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