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E. coli strains

E. coli strains. E. coli 0157 H7 strains lack efal, but do encode toxB, a tnmcated version of the efal gene. A toxB mutant exhibits reduced adherence to cultured epithelial cells (Stevens et ah, 2004). However, toxB had an indirect effect on adherence to epithelial cells by modulating the production and secretion of proteins that play a role for A/E formation in EHEC. The receptors for Efal and ToxB have not been identified and their true role in vivo is unknown. [Pg.125]

Additionally, we tested cell extracts in the colorimetric assay both negative control strains E. coli pET28a containing the empty vector and E. coli BFDL476Q (Table 2.2.1.2) did not show any enzyme activity in the TTC assay, whereas E. coli BAL (Table 2.2.1.2) led to the formation of an intense red color (data not shown). [Pg.306]

Only in the presence of 3,5-epimerase could a significant exchange of tritium be observed. One line of evidence consistent with this interpretation came from the use of a mutant strain E. coli Y-10, incapable of producing 6-deoxyhexose. When extracts of E. coli Y-10 were incubated with TDP-4-keto-6-deoxyglucose-3T, no exchange with the medium was observed. [Pg.405]

Overnight culture of the wild-type strain E. coli HB101 in the medium of choice. Other bacterial strains may also be used as required. [Pg.163]

Fig. 4.3.1. Schemes for genetic selection of DNA polymerase function based on complementation, (a) Host cells of E. coli recA718po/A12 that encodes a temperature-sensitive variant of DNA polymerase I (Pollts) are transformed with a polymerase mutant library. Active polymerase mutants substitute for DNA polymerase I at the non-permissive temperature (37 °C). (b) The host strain E. coli... Fig. 4.3.1. Schemes for genetic selection of DNA polymerase function based on complementation, (a) Host cells of E. coli recA718po/A12 that encodes a temperature-sensitive variant of DNA polymerase I (Pollts) are transformed with a polymerase mutant library. Active polymerase mutants substitute for DNA polymerase I at the non-permissive temperature (37 °C). (b) The host strain E. coli...
The earliest work with this bacterium showed that PolyPs occurred in it in extremely low amounts, if at all, and were present not continually and often under specific conditions, usually under growth limitation by some nutrient sources. Indeed, study of the dynamics of PolyP accumulation during the growth of the wild-type strain E. coli K12 on a mineral... [Pg.125]

Efremenko, E.N., Votchitseva, Yu.V., Aliev, T.K., and Varfolomeyev, S.D. (2005) Recombinant plasmid DNA pTES-His-OPH encoding synthesis of polypeptide with properties of organophosphate hydrolase, and strain E.coli - producer of polypeptide with properties of organophosphate hydrolase. Patent RU 2255975. [Pg.90]

In addition there is no problem with obelin availability for the present moment we have the hyper-producing strain E. coli of the protein available, and the technology permitting the obtaining of over 50 mg of a highly purified apoobelin per 1 g of raw cell paste. The recombinant apoprotein is effectively activated with a synthetic coelenterazine and does not differ from a native product in biochemical and bioluminescent properties. The protein is stable when stored in a soluble or lyophilized state. [Pg.463]

E. coli is a bacteriiun which typically inhabits the intestines of all animals. While the majority of E. coli strains are benign, there are several strains of E. coli that are capable of causing human illness. E. coli 0157 H7 is one such strain. E. coli 0157 H7 produces verotoxins that can cause severe damage to... [Pg.209]

Prepare an overnight culture of the assay strain, E. coli MT102 pJBA132 (luxR-P K/--RhSn-g (ASV)-To-Ti) (18) by growing the organism in 2 mL of ABt medium, with 6 pg/mL tetracycline at 3TC with shaking (200 rpm). [Pg.59]

The test to identify the minimal inhibitory concentration of E. coli was conducted using the strain E. coli IFA-No. 00-058,00. [Pg.17]

The cyanobacterial strain Anabaena variabilis PCC 29413 was maintained as described (3) on solid and liquid media supplemented with 10 mM HEPES pH 8.0. High CO2 cultures were stirred and bubbled with 2-5 % CO2 in air while low CO2 cultures were aerated with air alone (0.035 % CO2). The bacterial strains E.. coli HBlOl and JMlOl were maintained as described (4). Cyanobacterial genomic DNA and bacterial plasmid DNA was isolated essentially as described (5) with some modifications. Southern hybridization of restriction endonuclease fragments was performed with nitrocellulose membranes using P-labelled heterologous probes according to the manufacturer s specifications (S S). Total RNA isolation from Anabaena cells was performed as described (6) with some modifications. Northern hybridization was... [Pg.3268]

Recently, Bi et al. (2009) isolated En. asburiae JDR-1, a strain capable of fermenting both xylose and methylglucuronoxylose, which is released from hemicellulose upon acid treatment. The strain produced predominantly ethanol and acetate from hydrolysates of sweet gum xylan. To enhance ethanol production, the PET operon was introduced into En. asburiae JDR-1. Introduction of the PET operon led to homoethanol fermentation with acetate as a by-product. In addition, deletion of the native pfl gene enhanced ethanol production from xylan hydrolysates with 99% of theoretical yield and a rate of 0.11 g ethanol/L-h, which was 1.57 times the yield and 1.48 times the rate obtained with the ethanologenic strain E. coli KOI 1. [Pg.179]

Few platform organisms were suggested for fumaric acid production in addition to Rhizopus strains. E. coli has been chosen as a workhouse for the production of fumaric acid and many valuable chemicals including other organic... [Pg.427]


See other pages where E. coli strains is mentioned: [Pg.90]    [Pg.203]    [Pg.175]    [Pg.324]    [Pg.301]    [Pg.1510]    [Pg.181]    [Pg.331]    [Pg.13]    [Pg.238]    [Pg.543]    [Pg.402]    [Pg.85]    [Pg.195]    [Pg.93]    [Pg.597]    [Pg.576]    [Pg.218]    [Pg.34]    [Pg.21]    [Pg.76]    [Pg.81]    [Pg.368]    [Pg.371]    [Pg.163]    [Pg.75]    [Pg.144]    [Pg.122]    [Pg.175]    [Pg.342]    [Pg.345]    [Pg.393]    [Pg.760]    [Pg.328]    [Pg.1943]   
See also in sourсe #XX -- [ Pg.188 ]




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