Peter Rutledge

Dr. Peter Rutledge

School of Chemistry, The University of Sydney, NSW 2006, Australia
orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 June 2015 in Nature Reviews Microbiology
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Journal Article
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Peter RutledgePeter Rutledge
Peter Rutledge
GCGregory L. Challis
Gregory L. Challis

12 February 2020 in Chemical Science
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Journal Article
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AFAngelo Frei
Angelo Frei
JZJohannes Zuegg
Johannes Zuegg
AEAlysha G. Elliott
Alysha G. Elliott
MBMurray Baker
Murray Baker
SBStefan Bräse
Stefan Bräse
Mark BlaskovichMark Blaskovich
Mark Blaskovich
There is a dire need for new antimicrobial compounds to combat the growing threat of widespread antibiotic resistance. With a currently very scarce drug pipeline, consisting mostly of derivatives of known antibiotics, new classes of antibiotics are urgently required. Metal complexes are currently in clinical development for the treatment of cancer, malaria and neurodegenerative diseases. However, only little attention has been paid to their application as potential antimicrobial compounds. We report the evaluation of 906 metal-containing compounds that have been screened by the Community for Open Antimicrobial Drug Discovery (CO-ADD) for antimicrobial activity. Metal-bearing compounds display a significantly higher hit-rate (9.9%) when compared to the purely organic molecules (0.87%) in the CO-ADD database. Out of 906 compounds, 88 show activity against at least one of the tested strains, including fungi, while not displaying any cytotoxicity against mammalian cell lines or haemolytic properties. Herein, we highlight the structures of the 30 compounds with activity against Gram-positive and/or Gram-negative bacteria containing Mn, Co, Zn, Ru, Ag, Eu, Ir and Pt, with activities down to the nanomolar range against methicillin resistant S. aureus (MRSA). 23 of these complexes have not been reported for their antimicrobial properties before. This work reveals the vast diversity that metal-containing compounds can bring to antimicrobial research. It is important to raise awareness of these types of compounds for the design of truly novel antibiotics with potential for combatting antimicrobial resistance.

1 October 1999 in Nature
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NBNicolai I. Burzlaff
Nicolai I. Burzlaff
Peter RutledgePeter Rutledge
Peter Rutledge
ICIan J. Clifton
Ian J. Clifton
CHCharles M. H. Hensgens
Charles M. H. Hensgens
MPMichael Pickford
Michael Pickford
JBJack E. Baldwin
Jack E. Baldwin

28 January 2022 in Molecules
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HLHeather Jane Lacey
Heather Jane Lacey
Peter RutledgePeter Rutledge
Peter Rutledge
The Streptomyces genus has been a rich source of bioactive natural products, medicinal chemicals, and novel drug leads for three-quarters of a century. Yet studies suggest that the genus is capable of making some 150,000 more bioactive compounds than all Streptomyces secondary metabolites reported to date. Researchers around the world continue to explore this enormous potential using a range of strategies including modification of culture conditions, bioinformatics and genome mining, heterologous expression, and other approaches to cryptic biosynthetic gene cluster activation. Our survey of the recent literature, with a particular focus on the year 2020, brings together more than 70 novel secondary metabolites from Streptomyces species, which are discussed in this review. This diverse array includes cyclic and linear peptides, peptide derivatives, polyketides, terpenoids, polyaromatics, macrocycles, and furans, the isolation, chemical structures, and bioactivity of which are appraised. The discovery of these many different compounds demonstrates the continued potential of Streptomyces as a source of new and interesting natural products and contributes further important pieces to the mostly unfinished puzzle of Earth’s myriad microbes and their multifaceted chemical output.

8 April 2015 in Optics Letters
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AHArafat Hossain
Arafat Hossain
JCJohn Canning
John Canning
SASandra Ast
Sandra Ast
KCKevin Cook
Kevin Cook
Peter RutledgePeter Rutledge
Peter Rutledge
AJAbbas Jamalipour
Abbas Jamalipour
A combined “dual” absorption and fluorescence smartphone spectrometer is demonstrated. The optical sources used in the system are the white flash LED of the smartphone and an orthogonally positioned and interchangeable UV (λex=370  nm) and blue (λex=450  nm) LED. The dispersive element is a low-cost, nano-imprinted diffraction grating coated with Au. Detection over a 300 nm span with 0.42 nm/pixel resolution was carried out with the camera CMOS chip. By integrating the blue and UV excitation sources into the white LED circuitry, the entire system is self-contained within a 3D printed case and powered from the smartphone battery; the design can be scaled to add further excitation sources. Using a customized app, acquisition of absorption and fluorescence spectra are demonstrated using a blue-absorbing and green-emitting pH-sensitive amino-naphthalimide-based fluorescent probe and a UV-absorbing and blue-emitting Zn2+-sensitive fluoro-ionophore.

7 October 2014 in IEEE Sensors Journal
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Journal Article
Closed access
AHArafat Hossain
Arafat Hossain
JCJohn Canning
John Canning
SASandra Ast
Sandra Ast
Peter RutledgePeter Rutledge
Peter Rutledge
TYTeh Li Yen
Teh Li Yen
AJAbbas Jamalipour
Abbas Jamalipour
A novel portable fluorometer combining the attributes of a smartphone with an easy-fit, simple and compact sample chamber fabricated using 3-D printing has been developed for pH measurements of environmental water in the field. A color filter attached over the camera white light light-emitting diode selects an excitation band centered around λ ~ 450 nm with a 3-dB bandwidth, Δλ ~ 21 nm. An application-specific, temperature-stable probe based on the 4-aminonaphthalimide fluorophore was synthesized to absorb at this wavelength while emitting in the green region of the visible spectrum. The green emission is readily detected using the smartphone camera and a simple red-green-blue Android application. Suppression of the green emission increases with increasing pH enabling a straightforward pH sensor. The system was calibrated against a commercial spectrofluorometer and pH measurements were taken at various locations around Sydney. The results were then compared directly with those obtained using conventional electrode-based measurements. The data can be stored in the phone's available memory or transmitted by phone back to base for further real-time analysis.