Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Penicillinase

The yields of DNA intake by the cells are, however, very low. The few bacteria containing the hybrid plasmid need to be sorted out. One technique applies a plasmid which encodes for antibiotic-degrading enzymes, e.g for penicillinase and tetracyclinase, and thus... [Pg.244]

Directions for preparing a potentiometric biosensor for penicillin are provided in this experiment. The enzyme penicillinase is immobilized in a polyacrylamide polymer formed on the surface of a glass pH electrode. The electrode shows a linear response to penicillin G over a concentration range of 10 M to 10 M. [Pg.534]

Mifflin and associates described a membrane electrode for the quantitative analysis of penicillin in which the enzyme penicillinase is immobilized in a polyacrylamide gel that is coated on a glass pH electrode. The following data were collected for a series of penicillin standards. [Pg.536]

The substrate is amici11in for penicillinases and cephalothin for Cephases unless otherwise iadicated. The substrate is nitrocefin. [Pg.50]

The proper design of the side chains thus accessible has served not only to overcome many of the shortcomings of the early penicillins, such as acid lability, lack of oral activity, and ready destruction by bacterial penicillinase enzymes, but has provided antibiotics with broadened antibacterial spectra. [Pg.411]

Acylation of 6-APA by the naphthoic acid, 13, again affords an agent with considerable steric hindrance about the amide function. There is thus obtained the antibiotic nafcillin (14). a compound with good resistance to penicillinases. [Pg.412]

Acylation of 7-ACA with 2-thienylacetylchloride gives the amide cephalothin (43). Displacement of the allylic acetyl group by pyridine affords the corresponding pyridinium salt cephalori-dine (44). Both these compounds constitute useful injectable antibiotics with some activity against bacteria resistant to penicillin by reason of penicillinase production. [Pg.417]

This Crude product (15.8 g) In water (360 ml) was added to a prehydrogenated suspension of 10% palladium on charcoal (4 g) in water (400 ml), and hydrogenation was continued for 30 minutes. The catalyst was removed and the filtrate was adjusted to pH 7.5 with sodium bicarbonate, then evaporated at low temperature and pressure. The residue was purified by chromatography on a column of cellulose powder, eluting first with butanol/ ethanol/water mixture and then with acetone/isopropanol/water. The main fraction was evaporated at low temperature and pressure to give a 32% yield of the sodium salt of a-carboxybenzylpenicillin as a white powder. The product was estimated by manometric assay with penicillinase to be 58% pure. [Pg.236]

Penicillin can likewise be determined by using the enzyme penicillinase to destroy the penicillin with production of hydrogen ions which can be determined using a normal glass pH electrode. Many other organic materials can be determined by similar procedures.34,35... [Pg.562]

Gram-negative bacteria, had displayed resistance to hydrolysis by certain penicillinases and had die low toxicity of the penicillins. [Pg.180]

Class A Serine p-lactamases SHV-1 penicillinase in K. pneumoniae, and Koxy with activity against certain third generation cephalosporins in K. oxytoca BlaZ staphylococcal penicillinase TEM, SHV, VEB, PER and CTX-M penicillinases and ESBLs (P-lactamases with activity against third generation cephalosporins and aztreo-nam) KPC, IMI/NMC and SME carbapenemases... [Pg.771]

There are four groups of penicillins natural penicillins, penicillinase-resistant penicillins, aminopeni-cillins, and the extended-spectrum penicillins. See the... [Pg.65]

Because the natural penicillins have been used for many years, drug-resistant strains of microorganisms have developed, making the natural penicillins less effective than some of the newer antibiotics in treating a broad range of infections. Bacterial resistance has occurred within tire penicillins. Bacterial resistance is the ability of bacteria to produce substances that inactivate or destroy the penicillin. One example of bacterial resistance is tiie ability of certain bacteria to produce penicillinase, an enzyme that inactivates penicillin. The penicillinase-resistant penicillins were developed to combat this problem. [Pg.65]

Staphylococcus aureus is responsible for a variety of skin infections which require therapeutic approaches different from those of streptococcal infections. Staphylococcal celluhtis is indistinguishable clinically from streptococcal cellulitis and responds to cloxacillin or flucloxacillin, but generally fails to respond to penicillin owing to penicillinase (/3-lactamase) production. Staphylococcus aureus is an important cause of superficial, localized skin sepsis which varies ftom small pustules to boils and occasionally to a more deeply invasive, suppurative skin abscess known as a carbuncle. Antibiotics are generally not indicated for these conditions. Pustules and boils settle with antiseptic soaps or creams and often discharge spontaneously, whereas carbuncles frequently require surgical drainage. Staphylococcus aureus may also cause... [Pg.143]

Hydrolysis of penicillin mediated by penicillinase that has motivated attempts to alter its strnctnre (e.g., in semisynthetic penicillins). [Pg.170]

Catechins Bacteria Cell wall peptidoglycan 8-lactams Inhibition of penicillinase activity [67]... [Pg.253]

An immunoassay was developed to determine the penicillinase stable isoxazolyl penicillins cloxacillin and dicloxacillin in milk by Usleber et alJ The assay detected lOpgkg" of cloxacillin and 30pgkg of dicloxacillin with recoveries of 102% and 84%, respectively. The calibration curve was prepared by fortifying skimmed milk powder (lOOgL ) with standards. Fortified samples were prepared in pasteurized milk and analyzed directly after decreaming by centrifugation. This immunoassay was performed with minimal sample preparation, probably because the extensive water solubility of the penicillins prevents problems associated with more lipid-soluble analytes. [Pg.702]

The antibiotics of choice for treating methicillin-sensitive S. aureus (MSSA) infections are penicillinase-stable penicillins and first-generation cephalosporins. [Pg.1075]

Because GAS historically has been the primary causative organism, penicillin has been the mainstay of therapy. O However, the incidence ofS. aureus impetigo is increasing, so oral penicillinase-stable penicillins or first-generation cephalosporins are now preferred.3 Erythromycin is an alternative choice when penicillin allergy is a concern. Topical mupirocin may be used alone when there are few lesions.3... [Pg.1076]

In uncomplicated cases, prompt oral antibiotic therapy with amoxicillin or a first-generation cephalosporin halts the progression of lymphangitis. Clindamycin may be used if the patient has a significant (1-lactam allergy. Intravenous antibiotics (penicillinase-stable penicillins, first-generation cephalosporins,... [Pg.1076]


See other pages where Penicillinase is mentioned: [Pg.298]    [Pg.245]    [Pg.245]    [Pg.486]    [Pg.729]    [Pg.23]    [Pg.27]    [Pg.39]    [Pg.45]    [Pg.82]    [Pg.554]    [Pg.438]    [Pg.439]    [Pg.410]    [Pg.412]    [Pg.256]    [Pg.152]    [Pg.65]    [Pg.69]    [Pg.182]    [Pg.93]    [Pg.98]    [Pg.193]    [Pg.193]    [Pg.477]    [Pg.251]    [Pg.8]    [Pg.1078]   
See also in sourсe #XX -- [ Pg.410 ]

See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.300 , Pg.301 ]

See also in sourсe #XX -- [ Pg.375 , Pg.376 ]

See also in sourсe #XX -- [ Pg.2 ]




SEARCH



Bacillus cereus penicillinase

Bacillus cereus penicillinase induction

Bacillus licheniformis penicillinase

Bacteria gram-positive, penicillinase synthesis

Enzymes penicillinase (

Enzymes penicillinase reaction

Immobilization penicillinase

Penicillin Penicillinase

Penicillinase Penicillin-resistant Streptococcus

Penicillinase action

Penicillinase and

Penicillinase chromatography

Penicillinase discovery

Penicillinase messenger half-life

Penicillinase pneumoniae

Penicillinase resistant

Penicillinase resistant penicillin

Penicillinase synthesis

Penicillinase-resistance

Penicillinases inhibitors

The penicillinase-resistant penicillins are oxacillin, cloxacillin, dicloxacillin, methicillin, and nafcillin

© 2024 chempedia.info