Dirty money : a matter of bacterial survival, adherence, and toxicity

In this study we report the underlying reasons to why bacteria are present on banknotes and coins. Despite the use of credit cards, mobile phone apps, near-field-communication systems, and cryptocurrencies such as bitcoins which are replacing the use of hard currencies, cash exchanges still make up a significant means of exchange for a wide range of purchases. The literature is awash with data that highlights that both coins and banknotes are frequently identified as fomites for a wide range of microorganisms. However, most of these publications fail to provide any insight into the extent to which bacteria adhere and persist on money. We treated the various currencies used in this study as microcosms, and the bacterial loading from human hands as the corresponding microbiome. We show that the substrate from which banknotes are produced have a significant influence on both the survival and adherence of bacteria to banknotes. Smooth, polymer surfaces provide a poor means of adherence and survival, while coarser and more fibrous surfaces provide strong bacterial adherence and an environment to survive on. Coins were found to be strongly inhibitory to bacteria with a relatively rapid decline in survival on almost all coin surfaces tested. The inhibitory influence of coins was demonstrated through the use of antimicrobial disks made from coins. Despite the toxic effects of coins on many bacteria, bacteria do have the ability to adapt to the presence of coins in their environment which goes some way to explain the persistent presence of low levels of bacteria on coins in circulation. © 2016 by the authors; licensee MDPI, Basel, Switzerland. **Please note that there are multiple authors for this article therefore only the names of the Federation University Australia affiliates are is provided in this record*

Self-healing metal coordinated hydrogels using nucleotide ligands

A supramolecular gel formed by coordination of Zn2+ with adenosine monophosphate (AMP) is reported. The adenine base, the monophosphate, and Zn2+ are all important for gel formation. Mechanically disrupted gels can re-form upon centrifugation; applications of this gel for guest-molecule entrapment are explored.Beijing Higher Education Young Elite Teacher Project || ETP0520 Fundamental Research Funds for the Central Universities || YS1407 China Scholarship Council || Natural Sciences and Engineering Research Council |

Magnetic Iron Oxide Nanoparticle Seeded Growth of Nucleotide Coordinated Polymers

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Applied Materials & Interfaces, © 2016 American Chemical Society after peer review and technical editing by publisher. To access the final edited and published work see Liang, H., Liu, B., Yuan, Q., & Liu, J. (2016). Magnetic Iron Oxide Nanoparticle Seeded Growth of Nucleotide Coordinated Polymers. Acs Applied Materials & Interfaces, 8(24), 15615–15622. https://doi.org/10.1021/acsami.6b04038The introduction of functional molecules to the surface of magnetic iron oxide nanoparticles (NPs) is of critical importance. Most previously reported methods were focused on surface ligand attachment either by physisorption or covalent conjugation, resulting in limited ligand loading capacity. In this work, we report the seeded growth of a nucleotide coordinated polymer shell, which can be considered as a special form of adsorption by forming a complete shell. Among all of,the tested metal ions, Fe3+ is the most efficient for this seeded growth. A diverse range of guest molecules, including small organic dyes, proteins, DNA, and gold NPs, can be encapsulated in the shell. All of these molecules were loaded at a much higher capacity compared to that on the naked iron oxide NP core, confirming the advantage of the coordination polymer (CP) shell. In addition, the CP shell provides better guest protein stability compared to that of simple physisorption while retaining guest activity as confirmed by the entrapped glucose oxidase assay. Use of this system as a peroxidase nanozyme and glucose biosensor was demonstrated, detecting glucose as low as 1.4 mu M with excellent stability. This work describes a new way to functionalize inorganic materials with a biocompatible shell.Beijing Higher Education Young Elite Teacher Project [YETP0520]; Fundamental Research Funds for the Central Universities [YS1407]; Beijing Natural Science Foundation [2162030]; China Scholarship Council; Natural Sciences and Engineering Research Council of Canada (NSERC

3D-SeqMOS: A Novel Sequential 3D Moving Object Segmentation in Autonomous Driving

For the SLAM system in robotics and autonomous driving, the accuracy of front-end odometry and back-end loop-closure detection determine the whole intelligent system performance. But the LiDAR-SLAM could be disturbed by current scene moving objects, resulting in drift errors and even loop-closure failure. Thus, the ability to detect and segment moving objects is essential for high-precision positioning and building a consistent map. In this paper, we address the problem of moving object segmentation from 3D LiDAR scans to improve the odometry and loop-closure accuracy of SLAM. We propose a novel 3D Sequential Moving-Object-Segmentation (3D-SeqMOS) method that can accurately segment the scene into moving and static objects, such as moving and static cars. Different from the existing projected-image method, we process the raw 3D point cloud and build a 3D convolution neural network for MOS task. In addition, to make full use of the spatio-temporal information of point cloud, we propose a point cloud residual mechanism using the spatial features of current scan and the temporal features of previous residual scans. Besides, we build a complete SLAM framework to verify the effectiveness and accuracy of 3D-SeqMOS. Experiments on SemanticKITTI dataset show that our proposed 3D-SeqMOS method can effectively detect moving objects and improve the accuracy of LiDAR odometry and loop-closure detection. The test results show our 3D-SeqMOS outperforms the state-of-the-art method by 12.4%. We extend the proposed method to the SemanticKITTI: Moving Object Segmentation competition and achieve the 2nd in the leaderboard, showing its effectiveness

Multicopper Laccase Mimicking Nanozymes with Nucleotides as Ligands

This document is the Accepted Manuscript version of a Published Work that appeared in final form in Applied Materials & Interfaces, © 2017 American Chemical Society after peer review and technical editing by publisher. To access the final edited and published work see Liang, H., Lin, F., Zhang, Z., Liu, B., Jiang, S., Yuan, Q., & Liu, J. (2017). Multicopper Laccase Mimicking Nanozymes with Nucleotides as Ligands. Acs Applied Materials & Interfaces, 9(2), 1352–1360. https://doi.org/10.1021/acsami.6b15124Using nanomaterials to achieve functional enzyme mimics (nanozymes) is attractive for both applied and fundamental research. Laccases are multicopper oxidases highly important for biotechnology and environmental remediation. In this work, we report an exceptionally simple yet functional laccase mimic based on guanosine monophosphate (GMP) coordinated copper. It forms an amorphous metal organic framework (MOP) material. The ratio of copper and GMP is 3:4 as determined by isothermal titration calorimetry. It has excellent laccase-like activity and converts a diverse range of phenol containing substrates such as hydroquinone, naphthol, catechol and epinephrine. Comparative work shows that the activity is originated from guanosine coordination instead of phosphate binding in GMP. Cu2+ is required and cannot be substituted by other metal ions. At the same mass concentration, the Cu/GMP nanozyme has a higher V-max and similar K-m compared to the protein laccase. To achieve the same catalytic efficiency, the cost of the Gu/GMP is similar to 2400-fold lower than that of laccase. The Cu/GMP is much more stable at extreme pH, high salt, high temperature and for long-term storage. This is one of the first laccase-mimicking nanozymes, which will find important applications in analytical chemistry, environmental protection, and biotechnology.Beijing Natural Science Foundation [2162030]; Fundamental Research Funds for the Central Universities [YS1407]; China Scholarship Council; 111 project; Natural Sciences and Engineering Research Council of Canada (NSERC

Co-immobilization of multiple enzymes by metal coordinated nucleotide hydrogel nanofibers: improved stability and an enzyme cascade for glucose detection

Preserving enzyme activity and promoting synergistic activity via co-localization of multiple enzymes are key topics in bionanotechnology, materials science, and analytical chemistry. This study reports a facile method for co-immobilizing multiple enzymes in metal coordinated hydrogel nanofibers. Specifically, four types of protein enzymes, including glucose oxidase, Candida rugosa lipase, a-amylase, and horseradish peroxidase, were respectively encapsulated in a gel nanofiber made of Zn2+ and adenosine monophosphate (AMP) with a simple mixing step. Most enzymes achieved quantitative loading and retained full activity. At the same time, the entrapped enzymes were more stable against temperature variation (by 7.5 degrees C), protease attack, extreme pH (by 2-fold), and organic solvents. After storing for 15 days, the entrapped enzyme still retained 70% activity while the free enzyme nearly completely lost its activity. Compared to nanoparticles formed with AMP and lanthanide ions, the nanofiber gels allowed much higher enzyme activity. Finally, a highly sensitive and selective biosensor for glucose was prepared using the gel nanofiber to co-immobilize glucose oxidase and horseradish peroxidase for an enzyme cascade system. A detection limit of 0.3 mu M glucose with excellent selectivity was achieved. This work indicates that metal coordinated materials using nucleotides are highly useful for interfacing with biomolecules.Beijing Higher Education Young Elite Teacher Project [YETP0520]; Fundamental Research Funds for the Central Universities [YS1407]; Beijing Natural Science Foundation [2162030]; China Scholarship Council; Natural Sciences and Engineering Research Council of Canada (NSERC

A Polycistronic System for Multiplexed and Precalibrated Expression of Multigene Pathways in Fungi

Synthetic biology requires efficient systems that support the well-coordinated co-expression of multiple genes. Here, we discover a 9-bp nucleotide sequence that enables efficient polycistronic gene expression in yeasts and filamentous fungi. Coupling polycistronic expression to multiplexed, markerless, CRISPR/Cas9-based genome editing, we develop a strategy termed HACKing (Highly efficient and Accessible system by CracKing genes into the genome) for the assembly of multigene pathways. HACKing allows the expression level of each enzyme to be precalibrated by linking their translation to those of host proteins with predetermined abundances under the desired fermentation conditions. We validate HACKing by rapidly constructing highly efficient Saccharomyces cerevisiae cell factories that express 13 biosynthetic genes, and produce model endogenous (1,090.41 ± 80.92 mg 

Production of high‐purity hydrogen and layered doubled hydroxide by the hydrolysis of Mg‐Al alloys

Hydrogen is becoming an important clean energy and layered doubled hydroxide (LDH) is of great interest for many applications, including water treatment, environmental remediation, and chemical catalysis. The production of high‐purity hydrogen and LDH by the hydrolysis of Mg‐Al alloys is reported. The effects of initial pH, reaction temperature, reaction time, and alloy's Mg/Al mass ratio on the rate of hydrogen generation and the purity of LDH are evaluated and the solid hydrolysis products are characterized by different techniques. The initial rate of hydrogen generation increases with decreasing initial pH and increasing reaction temperature and Mg/Al ratio while the purity of LDH increases with Mg/Al ratio, reaction temperature and time. This study may provide a new, green, and sustainable approach for storage of hydrogen and material for water treatment