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Field of Research : Microbial Genetics
Status : Active
Field of Research : Bacteriology
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  • Researchers (31)
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  • Active Funded Activity

    Discovery Projects - Grant ID: DP200103074

    Funder
    Australian Research Council
    Funding Amount
    $496,608.00
    Summary
    Living on air: how do bacteria scavenge atmospheric trace gases? This project aims to determine the molecular and cellular basis of atmospheric trace gas oxidation by bacteria. Bacteria have a remarkable ability to adapt to resource limitation and environmental change by entering dormant states. Our research has shown they survive in this state by using atmospheric hydrogen and carbon monoxide as energy sources. This interdisciplinary project will determine how bacteria achieve this by elucidati .... Living on air: how do bacteria scavenge atmospheric trace gases? This project aims to determine the molecular and cellular basis of atmospheric trace gas oxidation by bacteria. Bacteria have a remarkable ability to adapt to resource limitation and environmental change by entering dormant states. Our research has shown they survive in this state by using atmospheric hydrogen and carbon monoxide as energy sources. This interdisciplinary project will determine how bacteria achieve this by elucidating the regulation, mechanism, and integration of the three uncharacterised enzymes that mediate this process. Outcomes and benefits include understanding of the processes that facilitate bacterial persistence, regulate atmospheric composition, and in turn support resilience of natural ecosystems.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP210100553

    Funder
    Australian Research Council
    Funding Amount
    $416,025.00
    Summary
    Bacterial polycyclic aromatic hydrocarbon transport and degradation. This project aims to investigate the molecular processes underpinning the degradation of polycyclic aromatic hydrocarbons (PAHs) by bacteria. PAHs are persistent environmental contaminants linked to several human diseases, including cancer. Bacteria capable of degrading PAHs could be used to naturally and effectively reduce environmental PAH loads to below safe levels. The project will apply techniques in functional genomics an .... Bacterial polycyclic aromatic hydrocarbon transport and degradation. This project aims to investigate the molecular processes underpinning the degradation of polycyclic aromatic hydrocarbons (PAHs) by bacteria. PAHs are persistent environmental contaminants linked to several human diseases, including cancer. Bacteria capable of degrading PAHs could be used to naturally and effectively reduce environmental PAH loads to below safe levels. The project will apply techniques in functional genomics and biochemistry to help define the ways that PAHs are taken up from the environment by bacteria, their fate within bacterial cells, and the ways that bacteria overcome the inherent toxicity of PAHs. The knowledge generated is expected to enhance our capacity to rationally deploy bacteria for PAH degradation.
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    Active Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE200101524

    Funder
    Australian Research Council
    Funding Amount
    $355,325.00
    Summary
    Taking Control: Understanding regulation of bacterial iron acquisition. This project aims to uncover the bacterial regulatory networks acting on a family of iron-stealing molecules called siderophores. Bacteria use siderophores to acquire iron from their hosts, the environment, and each other – as such, they have a central role in microbial life. Despite their importance, we have an incomplete knowledge of how these iron-stealing weapons are deployed. This project will develop a new genomics-bas .... Taking Control: Understanding regulation of bacterial iron acquisition. This project aims to uncover the bacterial regulatory networks acting on a family of iron-stealing molecules called siderophores. Bacteria use siderophores to acquire iron from their hosts, the environment, and each other – as such, they have a central role in microbial life. Despite their importance, we have an incomplete knowledge of how these iron-stealing weapons are deployed. This project will develop a new genomics-based, high-throughput technology for defining bacterial gene regulation networks, and use it to understand siderophore control. This will provide new knowledge of siderophore function, enhance understanding of bacterial community and host interactions, and establish leadership in a new genomics technology in Australia.
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    Active Funded Activity

    Australian Laureate Fellowships - Grant ID: FL210100258

    Funder
    Australian Research Council
    Funding Amount
    $3,331,707.00
    Summary
    Understanding how bacteria adapt and function in the complex gut ecosystem. This project aims to investigate the role of the gut ecosystem in defining the structure and function of microbes. Given that one of the current challenges in microbiology is our inability to study individual microbes directly from complex, multi-microbial niches, this project aims to develop multidisciplinary methods to study microbes in their native state, to understand how they adapt to live in the gut. This understan .... Understanding how bacteria adapt and function in the complex gut ecosystem. This project aims to investigate the role of the gut ecosystem in defining the structure and function of microbes. Given that one of the current challenges in microbiology is our inability to study individual microbes directly from complex, multi-microbial niches, this project aims to develop multidisciplinary methods to study microbes in their native state, to understand how they adapt to live in the gut. This understanding should provide fundamental insights into adaptation mechanisms that lead to bacterial proliferation, disease and antibiotic resistance. As well as enhancing interdisciplinary collaborations, this work should provide economic benefits by contributing to improved gut health of animals, and more efficient food production.
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    Active Funded Activity

    ARC Future Fellowships - Grant ID: FT180100123

    Funder
    Australian Research Council
    Funding Amount
    $874,125.00
    Summary
    Breaking through the Gram-negative cell barrier. This project aims to develop fundamental knowledge of the cell envelope in Gram-negative bacteria, which functions as a permeability barrier to small molecules. Combining innovative functional genomics with biochemistry, this project will determine how small molecules can pass across the cell envelope, and the chemical properties that they need to do so. Some Gram-negative bacteria are human pathogens and cause serious infections, whereas others a .... Breaking through the Gram-negative cell barrier. This project aims to develop fundamental knowledge of the cell envelope in Gram-negative bacteria, which functions as a permeability barrier to small molecules. Combining innovative functional genomics with biochemistry, this project will determine how small molecules can pass across the cell envelope, and the chemical properties that they need to do so. Some Gram-negative bacteria are human pathogens and cause serious infections, whereas others are used in biotechnology for biosynthetic chemical production or bioremediation. This project expects to help the future development of new antibiotics and assist in the design of strains to be used in biotechnological applications.
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    Active Funded Activity

    Discovery Early Career Researcher Award - Grant ID: DE200100111

    Funder
    Australian Research Council
    Funding Amount
    $373,097.00
    Summary
    Replication and transfer of novel plasmid classes in Acinetobacter. The project aims to reveal basic biology of plasmids found in Acinetobacter baumannii. A. baumannii is a bacterial pathogen that can rapidly acquire resistance to antibiotics, including last-resort antibiotics. In modern strains, acquisition is often mediated by plasmids. On the basis of DNA sequencing data, A. baumannii plasmids are likely to function differently to well-studied plasmids. However, surprisingly little experiment .... Replication and transfer of novel plasmid classes in Acinetobacter. The project aims to reveal basic biology of plasmids found in Acinetobacter baumannii. A. baumannii is a bacterial pathogen that can rapidly acquire resistance to antibiotics, including last-resort antibiotics. In modern strains, acquisition is often mediated by plasmids. On the basis of DNA sequencing data, A. baumannii plasmids are likely to function differently to well-studied plasmids. However, surprisingly little experimental work has been done to evidence this. By combining microbiological and bioinformatics approaches the project expects to generate new knowledge on the mechanisms of replication and transfer of A. baumannii plasmids. This may lead to new targets for strategies to slow and track the spread of antibiotic resistance.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP210103374

    Funder
    Australian Research Council
    Funding Amount
    $633,006.00
    Summary
    Mechanism of secretion of large clostridial toxins . This project aims to investigate how the large clostridial toxins are secreted from important animal bacterial pathogens. This project expects to generate new knowledge about how bacteria interact with hosts through protein secretion, using a collaborative and interdisciplinary approach and cutting-edge techniques. Expected outcomes of this project include building a deep understanding of the role of export machinery in toxin secretion from ba .... Mechanism of secretion of large clostridial toxins . This project aims to investigate how the large clostridial toxins are secreted from important animal bacterial pathogens. This project expects to generate new knowledge about how bacteria interact with hosts through protein secretion, using a collaborative and interdisciplinary approach and cutting-edge techniques. Expected outcomes of this project include building a deep understanding of the role of export machinery in toxin secretion from bacteria, and the identification of new systems by which this is achieved. This should provide significant benefits, such as gaining new insights into new bacterial protein export mechanisms, with the aim of identifying targets for future veterinary disease interventions or biotechnological applications.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP220101960

    Funder
    Australian Research Council
    Funding Amount
    $489,000.00
    Summary
    YhcB, a crucial player in the control of bacterial cell envelope biogenesis. All life depends on a cell envelope to enclose the chemical reactions that make life possible. But how do cell envelopes grow? How each component of the cell envelope is incorporated into the envelope at the right amount and in the right time to prevent cell death, has been a longstanding question in bacteriology. Using a unique combination of high through put genetic screens and biochemical approaches, this project wil .... YhcB, a crucial player in the control of bacterial cell envelope biogenesis. All life depends on a cell envelope to enclose the chemical reactions that make life possible. But how do cell envelopes grow? How each component of the cell envelope is incorporated into the envelope at the right amount and in the right time to prevent cell death, has been a longstanding question in bacteriology. Using a unique combination of high through put genetic screens and biochemical approaches, this project will characterise a key regulator of cell envelope growth in Gram-negative bacteria. Knowledge arising from this research will provide insight into a fundamental process in bacteria, will develop new technology to probe protein interactions, and will provide novel avenues to solve infection in plants, humans and animals.
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    Active Funded Activity

    Discovery Projects - Grant ID: DP190100827

    Funder
    Australian Research Council
    Funding Amount
    $390,000.00
    Summary
    Unravelling a novel stress-signalling system in bacteria. This project aims to investigate the cyclic-di-AMP signalling system in industrially important bacteria. The recently discovered cyclic-di-AMP is essential for normal bacterial growth and plays key roles in heat and antibiotic resistance, metabolism and virulence. This project will develop new biological assays to shed light on how bacteria sense and respond to environmental stress. Expected outcomes include a much deeper understanding of .... Unravelling a novel stress-signalling system in bacteria. This project aims to investigate the cyclic-di-AMP signalling system in industrially important bacteria. The recently discovered cyclic-di-AMP is essential for normal bacterial growth and plays key roles in heat and antibiotic resistance, metabolism and virulence. This project will develop new biological assays to shed light on how bacteria sense and respond to environmental stress. Expected outcomes include a much deeper understanding of signalling inputs and outputs. This should lead to benefits such as guiding the improvement of bacterial strains used in food and biochemical biotechnological applications, and may provide the foundation for the development of novel antibiotics.
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    Active Funded Activity

    Australian Laureate Fellowships - Grant ID: FL210100071

    Funder
    Australian Research Council
    Funding Amount
    $3,246,000.00
    Summary
    “L-form” bacteria: basic science, antibiotics, evolution and biotechnology. This Fellowship addresses key gaps in knowledge about cell wall deficient bacteria called L-forms: an altered state of bacteria with intriguing properties both structurally and functionally. The main aims of the research program are to improve our understanding of the basic biology of L-forms and employ them as tools in several important ways: for understanding the mechanisms of cell wall synthesis and how antibiotics wo .... “L-form” bacteria: basic science, antibiotics, evolution and biotechnology. This Fellowship addresses key gaps in knowledge about cell wall deficient bacteria called L-forms: an altered state of bacteria with intriguing properties both structurally and functionally. The main aims of the research program are to improve our understanding of the basic biology of L-forms and employ them as tools in several important ways: for understanding the mechanisms of cell wall synthesis and how antibiotics work, as models for early steps in the evolution of cellular life, and as a significant new platform for the production of proteins and fine chemicals. Outcomes and benefits include improved understanding of how to generate new antibiotics, and the development of new platforms for Australian biotechnology and biocommerce.
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