Displaying publications 1 - 20 of 1188 in total

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  1. Griffiths DA
    Can J Microbiol, 1966 Feb;12(1):149-63.
    PMID: 5923132
    Matched MeSH terms: Hydrogen-Ion Concentration
  2. Chandra N, Bhattathiry EP
    Trop Geogr Med, 1967 Dec;19(4):300-3.
    PMID: 5585976
    Matched MeSH terms: Hydrogen-Ion Concentration
  3. Ogle CW, Ng YT
    Med J Malaya, 1969 Mar;23(3):174-8.
    PMID: 4240069
    Matched MeSH terms: Hydrogen-Ion Concentration
  4. Hee Wan Jang H
    Med J Malaya, 1971 Mar;25(3):208-10.
    PMID: 4253248
    Matched MeSH terms: Hydrogen-Ion Concentration*
  5. Ng KH, Sen DK
    Med J Malaya, 1971 Dec;26(2):109-11.
    PMID: 4260854
    Matched MeSH terms: Hydrogen-Ion Concentration
  6. Varghese G
    Mycopathol Mycol Appl, 1972 Oct 09;48(1):43-61.
    PMID: 4677628
    Matched MeSH terms: Hydrogen-Ion Concentration
  7. Lie-Injo LE
    Med J Malaya, 1972 Dec;27(2):120-4.
    PMID: 4268037
    Matched MeSH terms: Hydrogen-Ion Concentration
  8. Welch QB, Lie-Injo LE
    Hum. Hered., 1972;22(5):503-7.
    PMID: 4670071
    Matched MeSH terms: Hydrogen-Ion Concentration
  9. West CE, Perrin DD, Shaw DC, Heap GH, Soemanto
    PMID: 4274568
    Matched MeSH terms: Hydrogen-Ion Concentration
  10. Soh KS, Chan KE
    Toxicon, 1974 Mar;12(2):151-8.
    PMID: 4859238
    Matched MeSH terms: Hydrogen-Ion Concentration
  11. Makar AB, McMartin KE, Palese M, Tephly TR
    Biochem Med, 1975 Jun;13(2):117-26.
    PMID: 1
    Matched MeSH terms: Hydrogen-Ion Concentration
  12. Moroi K, Sato T
    Biochem Pharmacol, 1975 Aug 15;24(16):1517-21.
    PMID: 8
    Matched MeSH terms: Hydrogen-Ion Concentration
  13. Marniemi J, Parkki MG
    Biochem Pharmacol, 1975 Sep 01;24(17):1569-72.
    PMID: 9
    Matched MeSH terms: Hydrogen-Ion Concentration
  14. Chow YW, Pietranico R, Mukerji A
    Biochem Biophys Res Commun, 1975 Oct 27;66(4):1424-31.
    PMID: 6
    Matched MeSH terms: Hydrogen-Ion Concentration
  15. Smith RJ, Bryant RG
    Biochem Biophys Res Commun, 1975 Oct 27;66(4):1281-6.
    PMID: 3
    Matched MeSH terms: Hydrogen-Ion Concentration
  16. Garner CW, Behal FJ
    Biochemistry, 1975 Nov 18;14(23):5084-8.
    PMID: 38
    The presence of at least two ionizable active center groups has been detected by a study of the effect of pH upon catalysis of hydrolysis of L-alanyl-beta-naphthylamide by human liver alanine aminopeptidase and upon the inhibition of hydrolysis by inhibitors and substrate analogs. Octanoic acid, octylamine, and peptide inhibitors have been found to be competitive inhibitors and are therefore thought to bind the active center. L-Phe was previously shown to bind the active center since it was found to be a competitive inhibitor of the hydrolysis of tripeptide substrates (Garner, C. W., and Behal, F. J. (1975), Biochemistry 14, 3208). A plot of pKm vs. pH for the substrate L-Ala-beta-naphthylamide showed that binding decreased below pH 5.9 and above 7.5, the points at which the theoretical curve undergoes an integral change in slope. These points are interpreted as the pKa either of substrate ionizable groups or binding-dependent enzyme active center groups. Similar plots of pKm vs. pH for L-alanyl-p-nitroanilide (as substrate) and pKi vs. pH for L-Leu-L-Leu-L-Leu and D-Leu-L-Tyr (as inhibitors) gave pairs fo pKa values of 5.8 and 7.4, 6.0 and 7.5, and 5.7 and 7.5, respectively. All the above substrates (and D-Leu-L-Tyr) have pKa values near 7.5; therefore, the binding-dependent group with a pKa value near 7.5 is possibly this substrate group. Similar plots of pKi vs. pH for the inhibitors L-Phe, L-Met, L-Leu, octylamine, and octanoic acid had only one bending point at 7.7, 7.6, 7.4, 6.3, and 5.9, respectively. Amino acid inhibitors, octylamine, and octanoic acid have no groups with pKa values between 5 and 9. These data indicate that there are two active center ionizable groups with pKa values of approximately 6.0 and 7.5 which are involved in substrate binding or inhibitory amino acid binding but not in catalysis since Vmax was constant at all pH values tested.
    Matched MeSH terms: Hydrogen-Ion Concentration
  17. Kidder GW, Montgomery CW
    Am J Physiol, 1975 Dec;229(6):1510-3.
    PMID: 2018
    We have recently shown that 5% CO2/95% O2 in the serosal bathing solution, with 100% O2 in the mucosal solution, results in CO2-diffusion limitation of acid secretion in bullfrog gastric mucosa. Changing to 10% CO2/90% 02 on both surfaces doubles the acid secretory rate. We calculate that, were the rate of oxygen consumption to increase significantly as a result of secretory stimulation, the tissue would now be oxygen limited. This prediction is tested by raising the P02 by increasing the total pressure in a hyperbaric chamber. Since no change in acid secretory rate or potential difference was observed upon changing from PO2 = 0.9 to PO2 = 1.9 atm, we conclude that the tissue is not O2 limited at normal pressure. Decreasing PO2 below 0.9 atm, by contrast, decreases the acid secretory rate and raises both PD and resistance. We infer that the rate of oxygen consumption did not rise significantly when acid secretion was increased by supplying sufficient CO2.
    Matched MeSH terms: Hydrogen-Ion Concentration
  18. Lambert DM
    J Hered, 1976 3 1;67(2):92-8.
    PMID: 5483
    The salivary chromosomes of four species of the nasuta complex of Drosophila, D. sulfurigaster albostrigata, D, kohkoa, D. albomicans, and D. kepulauana were studied and chromosome maps of each species are presented; the maps of the latter three species are based on the map of D. sulfurigaster albostrigata. Three of the species D. sulfurigaster albostrigata, D. albomicans, and D. kohkoa were shown to be highly polymorphic for chromosomal inversions while the available evidence indicated that D. kepulauana is much less polymorphic. These facts are correlated with the geographic distribution of the species. Transitional homoselection has not been complete in the evolution of three of the species since D. sulfurigaster albostrigata, D. kohkoa, and D. albomicans have a number of naturally occurring polymorphisms in common.
    Matched MeSH terms: Hydrogen-Ion Concentration
  19. Johanson RA, Reeves HC
    Biochim. Biophys. Acta, 1977 Jul 08;483(1):24-34.
    PMID: 18195
    Oxalacetate and glyoxylate are each weak inhibitors of NADP+-specific isocitrate dehydrogenase (threo-DS-isocitrate:NADP+ oxidoreductase (decarboxylating), EC 1.1.1.42)9 Together, however, they act in a concerted manner and strongly inhibit the enzyme. The rates of formation and dissociation of the enzyme inhibitor complex, and the rate of formation and the stability of the aldol condensation product of oxalacetate and glyoxylate, oxalomalate, were examined. The data obtained do not support the often suggested possibility that oxalomalate, per se, formed non-enzymatically in isocitrate dehydrogenase assay mixtures containing oxalacetate and glyoxylate, is responsible for the observed inhibition of the enzyme. Rather, the data presented in this communication suggest that oxalacetate binds to the enzyme first, and that the subsequent binding of glyoxylate leads to the formation of a catalytically inactive enzyme-inhibitor complex.
    Matched MeSH terms: Hydrogen-Ion Concentration
  20. Solberg T, Nesbakken T
    Nord Vet Med, 1981 Sep-Nov;33(9-11):446-53.
    PMID: 7329786
    The content of indole and the pH have been determined post mortem in shrimps (Pandalus borealis) caught in the Barents Sea and in shrimps caught outside Malaysia, India and Taiwan. These two criteria were compared with organoleptic assessment and the contents of volatile nitrogen bases (ammonia, trimethylamine) and living bacteria. For shrimps caught in the Barents Sea, both raw shrimps stored in ice and processed (broiled, peeled and single-frozen) shrimps were investigated. The results showed that only low levels of indole had been formed during ice-storage. Not until an advanced state of spoilage could a distinct increase in the indole content in raw and in boiled, peeled shrimps be discerned. pH increased slowly and varied in the area between acceptable and not acceptable quality. Neither the indole content nor the pH seems therefore to be a useful criterion for quality assessment either of raw shrimps caught in the Barents Sea or of such shrimps after processing (boiling and peeling). Most of the samples of boiled, peeled shrimps from the Far East were assessed organoleptically as less good-spoiled, and bacterial growth was significant. The content of trimethylamine oxide and volatile nitrogen was low, while the content of indole was high and exceeded 25 microgram/100 g in 8 or 14 samples. This is the upper limit for import in USA. The content of indole seems to be an important quality criterion for shrimps caught in warmer countries. The content of indole exceeded 25 microgram/100 g in some samples which were assessed organoleptically as acceptable. The pH was lower in brine-treated shrimps than in the others.
    Matched MeSH terms: Hydrogen-Ion Concentration
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