John Gustafson

Prof. John Gustafson

Department of Biochemistry and Molecular Biology, 246C Noble Research Center, Oklahoma State University, Stillwater, OK 74078-3035, USA
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Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

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

Representative Publications

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25 December 2001 in Journal of Applied Microbiology
Verified
Journal Article
Open access
PDF file
SCS. D. Cox
S. D. Cox
CMC. M. Mann
C. M. Mann
JMJ. L. Markham
J. L. Markham
HBH. C. Bell
H. C. Bell
John GustafsonJohn Gustafson
John Gustafson
SWS. G. Wyllie
S. G. Wyllie
S.D. COX, C.M. MANN, J.L. MARKHAM, H.C. BELL, J.E. GUSTAFSON, J.R. WARMINGTON and S.G. WYLLIE.2000.The essential oil of Melaleuca alternifolia (tea tree) exhibits broad‐spectrum antimicrobial activit...

16 January 2001 in Molecules
Verified
Journal Article
Open access
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SCSean D. Cox
Sean D. Cox
CMCindy M. Mann
Cindy M. Mann
JMJulie L. Markham
Julie L. Markham
John GustafsonJohn Gustafson
John Gustafson
JWJohn R. Warmington
John R. Warmington
SWS. Grant Wyllie
S. Grant Wyllie
Research into the mode of action of the essential oil of Melaleuca alternifolia (Tea tree oil) is briefly reviewed. Its mode of action is interpreted in terms of the membrane-toxicity of its monoterpenoid components and different approaches for determining cell membrane damage are discussed.

1 May 1998 in Letters in Applied Microbiology
Verified
Journal Article
Closed access
PDF file
SCS D Cox
S D Cox
John GustafsonJohn Gustafson
John Gustafson
CMC M Mann
C M Mann
JMJ L Markham
J L Markham
YLY C Liew
Y C Liew
SWS G Wyllie
S G Wyllie

1 March 1998 in Letters in Applied Microbiology
Verified
Journal Article
Closed access
PDF file
John GustafsonJohn Gustafson
John Gustafson
YLY C Liew
Y C Liew
SCS Chew
S Chew
JMJ Markham
J Markham
HBH C Bell
H C Bell
JWJ R Warmington
J R Warmington

1 October 2000 in The International Journal of Biochemistry & Cell Biology
Verified
Journal Article
Closed access
CPChristopher T.D Price
Christopher T.D Price
ILIan R Lee
Ian R Lee
John GustafsonJohn Gustafson
John Gustafson

1 July 1992 in Antimicrobial Agents and Chemotherapy
Verified
Journal Article
Closed access
BBB Berger-Bächi
B Berger-Bächi
ASA Strässle
A Strässle
John GustafsonJohn Gustafson
John Gustafson
FKF H Kayser
F H Kayser
Chromosomal factors, termed fem or aux factors, are needed for the expression of methicillin resistance in methicillin-resistant (Mcr) Staphylococcus aureus; also needed is the mec-encoded low-affinity penicillin-binding protein PBP 2'. These factors make up part of the normal set of genes present in susceptible and resistant strains of S. aureus and can be identified by Tn551-mediated insertional inactivation of the methicillin resistance. In this study, we characterized different Tn551 inserts and mapped them into four distinct loci on the SmaI chromosomal map of S. aureus NCTC 8325, thereby identifying two new loci which code for fem factors. The largest fragment, SmaI-A, carries three loci, two coding for both closely linked factors femA and femB and a novel third locus (femC) that is not linked to the other two. An additional, fourth, locus, femD, was identified in fragment SmaI-I. femA and femB inactivation reduced overall methicillin resistance, whereby femB had less of an influence on the resistance level. femC and femD inactivation reduced mainly the basal resistance level in heterogeneously Mcr strains and had less of an impact on the subpopulation with high-level resistance. Inactivation of either of these factors was shown to have no influence on the production of PBP 2', the main factor mediating methicillin resistance. In addition, no changes were observed in the banding patterns of the major autolysins in whole-cell extracts of the fem mutants, suggesting that the reduced cell wall turnover and autolysis observed in some of the insertionally inactivated strains were due to changes either of the substrate or in the autolysin control.