Purification and properties of an inducible cephalosporinase from Pseudomonas maltophilia GN12873.
An inducible cephalosporinase was purified from Pseudomonas maltophilia GN12873. The pI was 8.4, and the molecular weight was ca. 56,000 by gel filtration or 27,000 by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, suggesting that this enzyme had two subunits. The optimal pH and optimal...
保存先:
| 出版年: | Antimicrob Agents Chemother |
|---|---|
| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Microbiology (ASM)
1984
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC185518/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6609682/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.25.3.362 |
| タグ: |
タグなし, このレコードへの初めてのタグを付けませんか!
|