dc.contributor.author |
Hawkes, Jody. |
en_US |
dc.contributor.author |
Youngstown State University. College of Arts and Sciences. |
en_US |
dc.date.accessioned |
2011-01-31T14:20:30Z |
|
dc.date.accessioned |
2019-09-08T02:35:35Z |
|
dc.date.available |
2011-01-31T14:20:30Z |
|
dc.date.available |
2019-09-08T02:35:35Z |
|
dc.date.created |
2004 |
en_US |
dc.date.issued |
2004 |
en_US |
dc.identifier.other |
b19696024 |
en_US |
dc.identifier.uri |
http://jupiter.ysu.edu/record=b1969602 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/1989/6333 |
|
dc.description |
x, 70 leaves : ill. ; 29 cm. |
en_US |
dc.description |
Thesis (M.S.)--Youngstown State University, 2004. |
en_US |
dc.description |
Includes bibliographical references. |
en_US |
dc.description.abstract |
Bacillus subtilis is a Gram-positive bacterium capable of producing a wide range of
industrially important enzymes and antibiotics; making it a perfect subject for proteomicdrug
analysis. Here, B. subtilis will be grown with a minimum inhibitory concentration of
the macrolide class antibiotic Tylosin, which inhibits protein synthesis. The results were
compared to untreated B. subtilis control samples. Through two-dimensional gel analysis
and digital imaging software, it is seen that acidic shifting occurred in the treated
proteome expression profile indicating a chemical modification, via new isoelectric
points, during the exposure of B. subtilis to Tylosin. |
en_US |
dc.description.statementofresponsibility |
by Jody Hawkes. |
en_US |
dc.language.iso |
en_US |
en_US |
dc.relation.ispartofseries |
Master's Theses no. 0840 |
en_US |
dc.subject.classification |
Master's Theses no. 0840 |
en_US |
dc.subject.lcsh |
Bacillus subtilis. |
en_US |
dc.title |
Proteomic profiling of Bacillus subtilis with tylsoin [i.e. tylosin] / |
en_US |
dc.type |
Thesis |
en_US |