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  • LUNAR AND PLANETARY EXPLORATION  (14,409)
  • Biochemistry and Biotechnology  (13,095)
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  • 1
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    /Ar-39/-/Ar-40/ ages of lunar rocks (1977)
    In:  Other Sources
    Details
    Publication Date: 2019-07-13
    Description: The (Ar-39)-(Ar-40) ages for 21 lunar samples from Apollo 14, 15, 16, and 17 are presented. The cosmic-ray exposure ages, Ca, and K contents are also measured. Mare basalt 15075, a slowly cooled pyroxene-phyric basalt, has a (Ar-39)-(Ar-40) plateau age of 3.45 + or - 0.2 billion years. This is one of the oldest mare basalts found at Apollo 15. 65777, a recrystallized noritic breccia, has a plateau age of 3.72 + or - 0.02 billion years, relatively young for a highland rock. This rock is probably related to a cratering event over 200 m.y. post Imbrium. Similarly breccia 68516 was formed 150 m.y. post Imbrium. Histograms for the (Ar-39)-(Ar-40) plateau ages strongly suggest that the peak in ages at Apollo 14, 16, and 17 of about 4 billion years is caused by the dominance of Imbrium ejecta at these landing sites.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar Science Conference; Mar 14, 1977 - Mar 18, 1977; Houston, TX
    Format: text
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    NASA TECHNICAL REPORTS
  • 2
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    /Ar-40/-/Ar-39/ dating of Apollo 16 and 17 rocks (1975)
    In:  Other Sources
    Details
    Publication Date: 2019-07-13
    Description: The reported study is a continuation of an investigation begun by Alexander and Kahl (1974), with primary emphasis on (Ar-40)-(Ar-39) dating of lunar breccias. A primary objective of the study was related to the resolution of small plateau-age differences between Apollo 16 and 17 samples which have been irradiated in the same irradiation. This objective was not realized because (1) neither of the considered Apollo 16 samples has a well-defined plateau, and (2) the release patterns of the two Apollo 17 samples with plateaux (73235 and 77017) are sufficiently complex to suggest caution in interpretation of fine-scale differences among apparent ages. The plateau age of 73235 agrees well with plateau ages measured for a nearby boulder at the South Massif. The plateau age of 77017, on the other hand, agrees well with plateau ages measured in an nearby boulder at the base of the North Massif. These rock and boulder ages are tightly clustered about 3.99 b.y., and this clustering suggests that the North and South Massifs were made in the same basin-forming event, presumably Serenitatis.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar Science Conference; Mar 17, 1975 - Mar 21, 1975; Houston, TX
    Format: text
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    NASA TECHNICAL REPORTS
  • 3
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    /Ar-40/-/Ar-39/ dating of inclusions from IAB iron meteorites (1979)
    In:  Other Sources
    Details
    Publication Date: 2019-06-27
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Geochimica et Cosmochimica Acta; 43; Nov. 197
    Format: text
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    NASA TECHNICAL REPORTS
  • 4
    Electronic Resource
    Electronic Resource
    1,2-Dioxetanes: Novel chemiluminescent enzyme substrates. Applications to immunoassays (1989)
    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 4 (1989), S. 99-111 
    Details
    ISSN: 0884-3996
    Keywords: Chemiluminescent substrates ; enzymes ; immunoassays ; sensitive detection ; enhancement ; 1,2-dioxetane ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: We have synthesized and studied two 1,2-dioxetane-based chemiluminescent enzyme substrates: 3-(2′-spiroadamantane)-4-methoxy-4-(3″-phosphoryloxy)phenyl-1,2-dioxetane (AMPPD), and, 3-(2′-spiroadamantane)-4-methoxy-4- (3″-β-D′-galactopyrano-yloxy)phenyl-1,2-dioxetane (AMPGD), which can be activated to chemiluminescence at 470 nm by alkaline phosphatase and βD-galactosidase, respectively. In addition, we observed that certain macromolecules enhance the luminescence of AMPPD. For example, the addition of 0.1% bovine serum albumin amplifies the luminescent signal and improves the detection limit for alkaline phosphatase by approximately one order of magnitude under certain conditions. This effect is due to the presence of a hydrophobic microenvironment provided by the enhancer which ‘stabilizes’ the dephosphorylated AMPPD emitter.Alkaline phosphatase catalysed chemiluminescence from AMPPD is constant for a prolonged period of time. Using AMPPD we were able to detect 0.01 attomole quantities of alkaline phosphatase immobilized on membrane supports and imaged on photographic film and, in solution, measured in a luminometer.AMPPD and AMPGD offer alternatives to colorimetric and fluorescent subsrates for alkaline phosphatase and β-D-galactosidase labels used in enzyme immunoassays. The simplicity and sensitivity of this chemiluminescent readout allowed the development of rapid clinical assays (e.g. β-hCG, LH, TSH and others).
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bio.1170040116
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    Paper (German National Licenses)
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  • 5
    Electronic Resource
    Electronic Resource
    1,4-α-Glucan phosphorylase from Klebsiella pneumoniae covalently coupled on porous glass (1977)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 19 (1977), S. 1387-1403 
    Details
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A simplified procedure for the preparation of 1,4-α-glucan phosphorylase from Klebsiella pneumoniae is described. An 80-fold purification is achieved in two steps with an overall yield of about 50%. The specific activity of the homogeneous enzyme protein is 17.7 units/mg. Compared with glycogen phosphorylase from rabbit muscle the enzyme from K. pneumoniae shows a markedly higher stability against deforming and chaotropic agents. The 1,4-α-glucan phosphorylase was covalently bound to porous glass particles by three different methods. Coupling with glutaraldehyde gave the highest specific activity, i.e., 5.6 units/mg of bound protein or 133 units/g of glass with maltodextrin as substrate. This corresponds to about 30% of the specific activity of the soluble enzyme. With substrates of higher molecular weight, such as glycogen or amylopectin, lower relative activity was observed. The immobilized enzyme preparations showed pH activity profiles which were slightly displaced to higher values and exhibited an increased temperature stability.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260190911
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  • 6
    Electronic Resource
    Electronic Resource
    1-dehydrogenation of steroids by Septomyxa affinis (1962)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 4 (1962), S. 57-63 
    Details
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: 1-Dehydrogenation of steroids by Septomyxa affinis is brought about by an inducible enzyme. Only soluble substrate steroid is attacked. Individual steroids are dehydrogenated at different relative rates. The pH-activity curve is shallow.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260040108
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  • 7
    Electronic Resource
    Electronic Resource
    1-Monoglyceride production from lipase-catalyzed esterification of glycerol and fatty acid in reverse micelles (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 38 (1991), S. 507-517 
    Details
    ISSN: 0006-3592
    Keywords: lipases ; reverse micelles ; dynamic light scattering ; glycerol-fatty acid esterification ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Glycerol-fatty acid esterification has been conducted with lipase from R. delemar in water/AOT/isooctane reverse micellar media, with the major product being 1-monoglyceride, a useful food-emulsifier. 1,3-diglyceride was also synthesized, but to a much lesser extent. For a given set of initial conditions, the reaction productivity, measured in terms of the initial product formation rate, V0, and the final or equilibrium concentration of product, is optimal for a particular concentration of each surfactant, fatty acid, glycerol, and water. Many of these optimal values correlate well with a “critical” region on the phase diagram. Also, results indicate lipase-catalyzed esterification stops due to the achievement of kinetic equilibrium expect for a few cases where enzyme deactivation is severe. Dynamic light scattering was employed to examine the influence of water, glycerol, and fatty acid on micellar and interfacial structure. Results from this technique indicate enzyme kinetic are linked to interfacial phenomena and the presence of substrates at the interfacial region.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bit.260380509
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  • 8
    Electronic Resource
    Electronic Resource
    11th international symposium on glycoconjugates, 30 june-5 July 1991, Sheraton center, Toronto, Ontario, Canada (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    Cell Biochemistry and Function 8 (1990), S. 244-244 
    Details
    ISSN: 0263-6484
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cbf.290080413
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  • 9
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    12054 and 76215 - New measurements of interplanetary dust and solar flare fluxes (1977)
    In:  Other Sources
    Details
    Publication Date: 2019-07-13
    Description: The mass distribution and flux of micrometeoroids, variations in solar activity, solar-wind erosion and solar-flare track production are discussed on the basis of lunar sample analyses. A bimodal size frequency distribution of micrometeorites is found; the ratio of the density of craters larger than 0.1 micron to the density of those larger than 500 microns is 50 to 100 million. Solar cosmic-ray track ages determined for the lunar samples through use of the model of Blanford et al. (1975) indicate no variation in solar activity over a period of 2 million years. Solar wind erosion is set at no more than 0.03 A per year.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: Lunar Science Conference; Mar 14, 1977 - Mar 18, 1977; Houston, TX
    Format: text
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    NASA TECHNICAL REPORTS
  • 10
    Electronic Resource
    Electronic Resource
    13C tracer experiments and metabolite balancing for metabolic flux analysis: Comparing two approaches (1998)
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 58 (1998), S. 254-257 
    Details
    ISSN: 0006-3592
    Keywords: metabolic flux analysis ; 13C tracer experiments ; fractional enrichment ; NADH ; NADPH ; pentose phosphate pathway ; Aspergillus oryzae ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Conventional metabolic flux analysis uses the information gained from determination of measurable fluxes and a steady-state assumption for intracellular metabolites to calculate the metabolic fluxes in a given metabolic network. The determination of intracellular fluxes depends heavily on the correctness of the assumed stoichiometry including the presence of all reactions with a noticeable impact on the model metabolite balances. Determination of fluxes in complex metabolic networks often requires the inclusion of NADH and NADPH balances, which are subject to controversial debate. Transhydrogenation reactions that transfer reduction equivalents from NADH to NADPH or vice versa can usually not be included in the stoichiometric model, because they result in singularities in the stoichiometric matrix. However, it is the NADPH balance that, to a large extent, determines the calculated flux through the pentose phosphate pathway. Hence, wrong assumptions on the presence or activity of transhydrogenation reactions will result in wrong estimations of the intracellular flux distribution. Using 13C tracer experiments and NMR analysis, flux analysis can be performed on the basis of only well established stoichiometric equations and measurements of the labeling state of intracellular metabolites. Neither NADH/NADPH balancing nor assumptions on energy yields need to be included to determine the intracellular fluxes. Because metabolite balancing methods and the use of 13C labeling measurements are two different approaches to the determination of intracellular fluxes, both methods can be used to verify each other or to discuss the origin and significance of deviations in the results. Flux analysis based entirely on metabolite balancing and flux analysis, including labeling information, have been performed independently for a wild-type strain of Aspergillus oryzae producing α-amylase. Two different nitrogen sources, NH4+ and NO3-, have been used to investigate the influence of the NADPH requirements on the intracellular flux distribution. The two different approaches to the calculation of fluxes are compared and deviations in the results are discussed. © 1998 John Wiley & Sons, Inc. Biotechnol Bioeng 58:254-257, 1998.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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