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IN VITRO ANTIBACTERIAL ACTIVITY OF CEFOPERAZONE
The in vitro antibacterial activities of cefoperazone (CPZ) against clinical isolates including various-lactamase-producing strains were studied and compared with those of cefotiam (CTM).CPZ βhad a broad spectrum against Gram-negative and Gram-positive bacteria. Especially, CPZ showed apparently mor...
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Published in: | Japanese journal of antibiotics 1983/12/25, Vol.36(12), pp.3437-3443 |
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container_end_page | 3443 |
container_issue | 12 |
container_start_page | 3437 |
container_title | Japanese journal of antibiotics |
container_volume | 36 |
creator | WATANABE, YASUO MINAMI, SHINZABUROU YOTSUJI, AKIRA ARAKI, HARUMI YASUDA, TAKASHI SAIKAWA, ISAMU |
description | The in vitro antibacterial activities of cefoperazone (CPZ) against clinical isolates including various-lactamase-producing strains were studied and compared with those of cefotiam (CTM).CPZ βhad a broad spectrum against Gram-negative and Gram-positive bacteria. Especially, CPZ showed apparently more potent antibacterial activities than CTM against Enterobacter cloacae, Serratia marcescens, and Pseudomonas aeruginosa.However, CPZ was less active than CTM against Staphylococcus aureus and Proteus mirabilis. The stability and affinity of CPZ for various types of β-lactamase were also studied.CPZ was more resistant to hydrolysis by typical cephalosporinase (CSase) and cefuroximase (CXase) than CTM, but was less stable to penicillinase (PCase).CPZ often showed higher affinity to β-lactamases than CTM.The study for the inducer-activity revealed that CPZ hardly induced CSase production in E. cloacae and Proteus vulgaris while CTM highly induced in both strains. CPZ was more active against CSase-producers than CTM, especially against strains which inducibly produced the enzyme.It was speculated that this activity was responsible for the superior stability to CSase and low inducer-activity for CSase production. |
doi_str_mv | 10.11553/antibiotics1968b.36.3437 |
format | article |
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Especially, CPZ showed apparently more potent antibacterial activities than CTM against Enterobacter cloacae, Serratia marcescens, and Pseudomonas aeruginosa.However, CPZ was less active than CTM against Staphylococcus aureus and Proteus mirabilis. The stability and affinity of CPZ for various types of β-lactamase were also studied.CPZ was more resistant to hydrolysis by typical cephalosporinase (CSase) and cefuroximase (CXase) than CTM, but was less stable to penicillinase (PCase).CPZ often showed higher affinity to β-lactamases than CTM.The study for the inducer-activity revealed that CPZ hardly induced CSase production in E. cloacae and Proteus vulgaris while CTM highly induced in both strains. 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J. Antibiotics</addtitle><description>The in vitro antibacterial activities of cefoperazone (CPZ) against clinical isolates including various-lactamase-producing strains were studied and compared with those of cefotiam (CTM).CPZ βhad a broad spectrum against Gram-negative and Gram-positive bacteria. Especially, CPZ showed apparently more potent antibacterial activities than CTM against Enterobacter cloacae, Serratia marcescens, and Pseudomonas aeruginosa.However, CPZ was less active than CTM against Staphylococcus aureus and Proteus mirabilis. The stability and affinity of CPZ for various types of β-lactamase were also studied.CPZ was more resistant to hydrolysis by typical cephalosporinase (CSase) and cefuroximase (CXase) than CTM, but was less stable to penicillinase (PCase).CPZ often showed higher affinity to β-lactamases than CTM.The study for the inducer-activity revealed that CPZ hardly induced CSase production in E. cloacae and Proteus vulgaris while CTM highly induced in both strains. CPZ was more active against CSase-producers than CTM, especially against strains which inducibly produced the enzyme.It was speculated that this activity was responsible for the superior stability to CSase and low inducer-activity for CSase production.</description><subject>Bacteria - drug effects</subject><subject>Bacteria - enzymology</subject><subject>beta-Lactamases - biosynthesis</subject><subject>Cefoperazone - pharmacology</subject><subject>Drug Resistance, Microbial</subject><subject>Enzyme Induction - drug effects</subject><issn>0368-2781</issn><issn>2186-5477</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><recordid>eNpdUMtKw0AUHUSppfYThLhxl3YmN5nHMoZEA6GREgXdDDPJVFPSh5l04d87paULN_d1Dod7DkIPBM8IiSKYq-3Q6nY3tLUlgnI9AzqDENgVGgeEUz8KGbtGYwyU-wHj5BZNrW01BsJ44CRGaEQpFkFExmieL7z3vFqWXryo8qc4qdJlHheeG3J3__DKzEvSrHxNl_FnuUjv0M1KddZMz32C3rK0Sl78onzOk7jw10TgwY-g5kaIkDCGicahcb_QlQCsNMZubQwn4coEUR0KLLSuG-eDgREhkIZrARP0eNLd97ufg7GD3LS2Nl2ntmZ3sJJjLkAAd8T7M_GgN6aR-77dqP5Xnh06vDjhazuoL3PBVe_y64z8H6YEKklwrMdIL7T6W_XSbOEPqxZs5Q</recordid><startdate>198312</startdate><enddate>198312</enddate><creator>WATANABE, YASUO</creator><creator>MINAMI, SHINZABUROU</creator><creator>YOTSUJI, AKIRA</creator><creator>ARAKI, HARUMI</creator><creator>YASUDA, TAKASHI</creator><creator>SAIKAWA, ISAMU</creator><general>Japan Antibiotics Research Association</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>198312</creationdate><title>IN VITRO ANTIBACTERIAL ACTIVITY OF CEFOPERAZONE</title><author>WATANABE, YASUO ; MINAMI, SHINZABUROU ; YOTSUJI, AKIRA ; ARAKI, HARUMI ; YASUDA, TAKASHI ; SAIKAWA, ISAMU</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j190t-53c8e99417701b04e3686f930ab0004ede814fe25c4909bbcd68b73e9431d8b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1983</creationdate><topic>Bacteria - drug effects</topic><topic>Bacteria - enzymology</topic><topic>beta-Lactamases - biosynthesis</topic><topic>Cefoperazone - pharmacology</topic><topic>Drug Resistance, Microbial</topic><topic>Enzyme Induction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WATANABE, YASUO</creatorcontrib><creatorcontrib>MINAMI, SHINZABUROU</creatorcontrib><creatorcontrib>YOTSUJI, AKIRA</creatorcontrib><creatorcontrib>ARAKI, HARUMI</creatorcontrib><creatorcontrib>YASUDA, TAKASHI</creatorcontrib><creatorcontrib>SAIKAWA, ISAMU</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese journal of antibiotics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WATANABE, YASUO</au><au>MINAMI, SHINZABUROU</au><au>YOTSUJI, AKIRA</au><au>ARAKI, HARUMI</au><au>YASUDA, TAKASHI</au><au>SAIKAWA, ISAMU</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IN VITRO ANTIBACTERIAL ACTIVITY OF CEFOPERAZONE</atitle><jtitle>Japanese journal of antibiotics</jtitle><addtitle>Jpn. J. Antibiotics</addtitle><date>1983-12</date><risdate>1983</risdate><volume>36</volume><issue>12</issue><spage>3437</spage><epage>3443</epage><pages>3437-3443</pages><issn>0368-2781</issn><eissn>2186-5477</eissn><abstract>The in vitro antibacterial activities of cefoperazone (CPZ) against clinical isolates including various-lactamase-producing strains were studied and compared with those of cefotiam (CTM).CPZ βhad a broad spectrum against Gram-negative and Gram-positive bacteria. Especially, CPZ showed apparently more potent antibacterial activities than CTM against Enterobacter cloacae, Serratia marcescens, and Pseudomonas aeruginosa.However, CPZ was less active than CTM against Staphylococcus aureus and Proteus mirabilis. The stability and affinity of CPZ for various types of β-lactamase were also studied.CPZ was more resistant to hydrolysis by typical cephalosporinase (CSase) and cefuroximase (CXase) than CTM, but was less stable to penicillinase (PCase).CPZ often showed higher affinity to β-lactamases than CTM.The study for the inducer-activity revealed that CPZ hardly induced CSase production in E. cloacae and Proteus vulgaris while CTM highly induced in both strains. CPZ was more active against CSase-producers than CTM, especially against strains which inducibly produced the enzyme.It was speculated that this activity was responsible for the superior stability to CSase and low inducer-activity for CSase production.</abstract><cop>Japan</cop><pub>Japan Antibiotics Research Association</pub><pmid>6609251</pmid><doi>10.11553/antibiotics1968b.36.3437</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 0368-2781 |
ispartof | The Japanese Journal of Antibiotics, 1983/12/25, Vol.36(12), pp.3437-3443 |
issn | 0368-2781 2186-5477 |
language | jpn |
recordid | cdi_proquest_miscellaneous_80893938 |
source | Alma/SFX Local Collection |
subjects | Bacteria - drug effects Bacteria - enzymology beta-Lactamases - biosynthesis Cefoperazone - pharmacology Drug Resistance, Microbial Enzyme Induction - drug effects |
title | IN VITRO ANTIBACTERIAL ACTIVITY OF CEFOPERAZONE |
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