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bài 8 quang hợp ở các nhóm thực vật

VIBRATION AND SHOCK

VIBRATION AND SHOCK

Kĩ thuật Viễn thông

... 180 ° By taking the square root of 0.752 plus 1.162, we get a resultant of 1. 38 oz-in Now to get the proper angle: ^4 = 180 ° - tan-1 ^ - 180 ° - 32 .8 - 147.2° So we see that we must remove 1. 38 ... 102 020 102 000 = 9-^A 10 nm 100 nm /mi 10 ptm 100 fjan mm 10 mm 1m fN (Hz) 980 576 4 98 157.6 49 .8 15.76 4. 98 0.4 98 Note, from Eqs (23.2a) and (23.2b), that fN depends on 6, and thus on both ... imbalance at station 3, when sensed at station 1, is X 5A2 = % = 0 .83 or a vector 0 .83 at 180 ° By taking the square root of 2.252 plus 0 .83 2, we find that we must remove 2.41 oz-in Now at what angle...
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Bài giảng Chapter 17 Free Energy and Thermodynamics

Bài giảng Chapter 17 Free Energy and Thermodynamics

Hóa học

... H2O(g) HF(g) HBr(g) I2(s) N2(g) NO(g) Na(s) S(s) 28. 3 152.3 2.43 197.9 41.4 33.30 27.15 130. 58 188 .83 173.51 1 98. 49 116.73 191.50 210.62 51.45 31 .88 Al2O3(s) Br2(g) C(graphite) CO2(g) CaO(s) CuO(s) ... 6(SH O( g ) )] − [4(S NH ( g ) ) + 5(SO ( g ) )] J J J J = [ 4(210 .8 K ) + 6( 188 .8 K )] − [4(192 .8 K ) + 5(205.2 K )] J = 1 78. 8 K Check: ∆S is +, as you would expect for a reaction with more gas ... I2(g) NH3(g) NO2(g) O2(g) SO2(g) -1669 .8 +30.71 -393.5 -635.5 -156.1 -82 2.16 - 187 .8 - 285 .83 -92.30 +25.94 +62.25 -46.19 +33 .84 -296.9 Entropy • entropy is a thermodynamic function that increases...
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Tài liệu Báo cáo khoa học: Crystal structure of the cambialistic superoxide dismutase from Aeropyrum pernix K1 – insights into the enzyme mechanism and stability pdf

Tài liệu Báo cáo khoa học: Crystal structure of the cambialistic superoxide dismutase from Aeropyrum pernix K1 – insights into the enzyme mechanism and stability pdf

Báo cáo khoa học

... 0.0 08 1.135 6 984 29 630 31 .86 –1.35 (1. 38 1.35) 152991 (1 083 8) 18. 8 (23.9) ⁄ 20.3 (25.4) 0.0 08 1.170 682 3 18 734 49.75–1. 48 (1.52–1. 48) 113539 (7965) 22.6 (29.5) ⁄ 25.6 (32.7) 0.012 1. 382 685 5 ... 15.9 (5 .8) 13 .8 a = 69.06 b = 71.76 c = 76.40 b = 91.72 50.0–1. 48 (1.53–1. 48) 1.92 7.7 ( 38. 3) 95.9 (88 .9) 732659 124631 6.1 (5.2) 16.6 (3.6) 18. 3 36.13–1.57 (1.61–1.57) 987 31 (6 589 ) 19 .8 (33.7) ... (1.62–1.56) 1.95 7.3 (39.6) 98. 0 (92.4) 45 483 3 106 085 4.4 (2.7) 18. 1 (2.9) 19 .8 BL44XU, SPring -8 0.9 P21 a = 69.06 b = 71. 78 c = 76 .85 b = 91 .81 50.0–1.35 (1.40–1.35) 1.94 4 .8 (36.1) 98. 0 (97.0) 1179512...
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Tài liệu Báo cáo khóa học: Mutations in the hydrophobic core and in the protein–RNA interface affect the packing and stability of icosahedral viruses doc

Tài liệu Báo cáo khóa học: Mutations in the hydrophobic core and in the protein–RNA interface affect the packing and stability of icosahedral viruses doc

Báo cáo khoa học

... plaqueforming units Titer (p.f.u.ÆmL)1) Control MS2 T45S M88V D11N 3.4 kbar of pressure 4.5 M urea 9.0 M urea 1 08 1 08 1 08 1 08 1 08 1 08 107 1 08 105 102 102 107 ND ND ND 102 and T45S particles with ... RNA interaction (I) [U]½ (M) CM LS DV/na (mLÆmol)1) WT M88V T45S D11N B I S 4.6 3.2 3.0 5 .8 3.0 1.6 1 .8 >3.2 3.1 1.4 1.5 >3.2 4.65 19 .81 14.12 – a The apparent volume change of association (DV) ... and M88V were also coupled, as shown by the overlapping of the fluorescence and light scattering curves The large red-shift in the fluorescence emission spectra of the WT form and T45S, M88V and...
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Tài liệu Báo cáo khoa học: Relationships between structure, function and stability for pyridoxal 5¢-phosphate-dependent starch phosphorylase from Corynebacterium callunaeas revealed by reversible cofactor dissociation studies doc

Tài liệu Báo cáo khoa học: Relationships between structure, function and stability for pyridoxal 5¢-phosphate-dependent starch phosphorylase from Corynebacterium callunaeas revealed by reversible cofactor dissociation studies doc

Báo cáo khoa học

... the range 080 mM Protein KdPi (mM) Recovered enzyme activity (%) Wild-type S224A R226A R234A R242A 6.07 2 .89 10.4 47.1 ND 66 59 85 68 56 1.29 0.51 3 .8 4.5 (37) (35) ( 48) (15) ( 48) recovered ... PL-phosphorylase 1.050 /80 50/5120 50 /80 Native phosphorylase 1.050 /80 Activator oxyanion (mM) vmax (Uặmg)1) Km (mM) Phosphite (10) Phosphite (10) Phosphate (0.13.0) 1 .86 0.11 1.95 0.12 8. 6 0.2 11.2 ... 5Â-phosphate analogs Biochemistry 8, 5 189 5196 11 Shimomura, S., Emman, K & Fukui, T (1 980 ) The role of pyridoxal 5Â-phosphate in plant phosphorylase J Biochem 87 , 1043 1052 12 Tagaya, M., Shimomura,...
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VITAMINS IN FOODS Analysis, Bioavailability, and Stability potx

VITAMINS IN FOODS Analysis, Bioavailability, and Stability potx

Hóa học - Dầu khí

... 379 380 380 380 381 381 381 382 382 382 383 385 385 385 386 386 387 387 387 388 388 388 389 390 390 391 19 .8. 3 Columns 19 .8. 4 Applications to Food ... 2 58 260 262 263 264 264 275 276 276 277 277 2 78 2 78 2 78 279 281 281 282 283 283 283 284 284 284 285 285 Chapter 15 Vitamin C 15.1 Background 289 ... 57 60 61 61 62 63 63 63 66 66 67 67 67 68 68 69 69 71 74 74 76 77 77 77 78 80 81 86 87 88 88 88 3.6.2 Effects of b-Carotene Supplementation on Breastmilk Carotenoids...
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Báo cáo khoa học: Local changes in the catalytic site of mammalian histidine decarboxylase can affect its global conformation and stability pptx

Báo cáo khoa học: Local changes in the catalytic site of mammalian histidine decarboxylase can affect its global conformation and stability pptx

Báo cáo khoa học

... catalytic group and enhances catalysis J Biol Chem 2 78, 9 481 –9 488 48 Hayashi, H (1995) Pyridoxal enzymes: mechanistic diversity and uniformity J Biochem 1 18, 463–473 ... analysis of the coenzyme and reaction intermediates Biochemistry 32, 81 2 81 8 Hayashi, H., Mizugushi, H & Kagamiyama, H (19 98) The iminepyridine torsion of the pyridoxal 5¢-phosphate Schiff base ... USA 87 , 733– 737 33 Laemmli, U.K (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4 Nature 227, 680 – 685 34 Hayashi, H., Tanase, S & Snell, E.E (1 986 )...
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Arsenic speciation in environmental and biological samples extraction and stability studies

Arsenic speciation in environmental and biological samples extraction and stability studies

Môi trường

... species 3.0 7.9 7.0 80 .7 98. 6 ± ± ± ± ± 0.9 1.0 1.0 3.1 3.4 3.2 8. 1 7.3 80 .4 99.0 ± ± ± ± ± 1.0 1.1 1.0 3.2 3.6 2.9 8. 3 7.1 80 .4 98. 7 ± ± ± ± ± 0 .8 1.3 1.0 3.2 3.7 3.2 8. 3 7.2 80 .1 98. 8 ± ± ± ± ± 1.0 ... 3.1 8. 2 7.3 80 .0 98. 6 ± ± ± ± ± 1.0 2.0 2.0 3.2 4.2 As(III) DMA MMA As(V) As species 3.0 8. 1 7.1 80 .0 98. 2 ± ± ± ± ± 0 .8 1.0 1.0 3.6 3.9 3.3 8. 1 7.2 80 .2 98. 8 ± ± ± ± ± 1.0 1.4 1.1 3.3 3.9 3.1 8. 0 ... 3.0 28. 0 ± 1.9 85 .0 ± 3.7 50.0 ± 2.9 18. 0 ± 2.0 80 .0 ± 3.5 46.0 ± 2.2 12.2 ± 2.5 68. 0 ± 2.9 50.0 ± 3.0 20.0 ± 2.2 89 .0 ± 3.5 82 .0 ± 3.0 17.0 ± 2.0 99.0 ± 3.0 Certified values of NIST 1568a (0.29...
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BIS Papers No 62 Financial sector regulation for growth, equity and stability doc

BIS Papers No 62 Financial sector regulation for growth, equity and stability doc

Tài chính doanh nghiệp

... reproduced or translated provided the source is stated ISSN 1609-0 381 (print) ISBN 92-9131- 088 -3 (print) ISSN 1 682 -7651 (online) ISBN 92-9197- 088 -3 (online) Preface The failure of regulation and the short-sightedness ... 45 Summary of the discussion 85 Financial Sector Regulation for Equity Chair’s initial remarks Stephany Griffith-Jones 89 Too big to fail vs Too small to be counted ... real sectors: a critical survey of the literature”, BCBS Working Papers, no 18, February 2011 (www.bis.org/publ/bcbs_wp 18. htm) This is further elaborated in Committee on the Global Financial System,...
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Báo cáo khoa học: Increased amylosucrase activity and specificity, and identification of regions important for activity, specificity and stability through molecular evolution doc

Báo cáo khoa học: Increased amylosucrase activity and specificity, and identification of regions important for activity, specificity and stability through molecular evolution doc

Báo cáo khoa học

... G 184 A, C1317T, G1516A G99A, G495A, A1159G G1221T, G 183 9T A 680 G C123T, G1165C, A1509T C58T, G444T, T1793C N76D P157A, D231Y P234L, G554S E62K, D506N N 387 D Q613H E227G V 389 L, N503I R20C, F598S ... (57) 570 (52) 555 (42) H4 580 (62) 595 (84 ) 605 (1 08) 600 (94) 605 (1 08) 585 ( 68) E9 nd nd 570 (52) 580 (62) 570 (52) 560 (45) FEBS Journal 273 (2006) 673– 681 ª 2006 The Authors Journal compilation ... ⁄ Km2 (s)1ÆmM)1) 0.74 0.60 1.19 0.19 0.14 0. 28 71 165 82 1.4 1.7 2.2 0.020 0.010 0.026 0.35 0. 18 0.54 0.14 0.23 0.23 29 48 62 0.52 0.43 0 .86 0.0 18 0.009 0.014 0.43 (1.2)a 0.05 0.36 (2.0) 0.04...
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Báo cáo khoa học: Thermodynamic analysis of the unfolding and stability of the dimeric DNA-binding protein HU from the hyperthermophilic eubacterium Thermotoga maritima and its E34D mutant pdf

Báo cáo khoa học: Thermodynamic analysis of the unfolding and stability of the dimeric DNA-binding protein HU from the hyperthermophilic eubacterium Thermotoga maritima and its E34D mutant pdf

Báo cáo khoa học

... denaturation of Sac7d J Mol Biol 264, 784 80 5 Jaenicke, R & Bohm, G (19 98) The stability of proteins in ¨ extreme environments Curr Opin Struct Biol 8, 7 38 7 48 Szilagyi, A & Zavodsky, P (2000) Structural ... ± ± ± ± ± ± 0.2 0.2 0.2 0.2 0.3 0.3 DGU,25 (kJÆmol)1) Tg (°C) 183 175 174 166 106 100 28. 5 26.7 26.6 25.0 16.0 15.4 101.9 98. 0 97 .8 94.2 74.4 73.0 ± ± ± ± ± ± 2 2 3 ± ± ± ± ± ± 0.3 0.3 0.3 0.3 ... 19 White, S.W., Appelt, K., Wilson, K.S & Tanaka, I (1 989 ) A protein structural motif that bends DNA Proteins Struct Funct Genet 5, 281 – 288 20 Vis, H., Mariani, M., Vorgias, C.E., Wilson, K.S.,...
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Báo cáo khoa học: Solution structure and stability of the full-length excisionase from bacteriophage HK022 pot

Báo cáo khoa học: Solution structure and stability of the full-length excisionase from bacteriophage HK022 pot

Báo cáo khoa học

... 6.5 6.5b 7.0 41.6 47.3 51.4 51.9 54.0 1 38 153 165 165 174 2 .8 2 .8 3.1 3.0 3.0 82 82 76 74 74 0.26 0.25 0.22 0.21 0.21 6.9 8. 2 9 .8 9.9 11.0 0.91 0.96 0. 98 0. 98 0.99 a Data for the Xis_wt thermal ... binding J Bacteriol 182 , 580 7– 581 2 Supplementary material The following material is available from http://blackwell publishing.com/products/journals/suppmat/EJB/EJB 388 4/ EJB 388 4sm.htm Appendix S1 ... local RMSD values Interaction of HK022 Xis with specific DNA (X1) 21 0.36 0 .83 1 .86 0.71 1. 68 ± ± ± ± 0.14 0. 18 0.13 0.19 83 .9 13.1 1.6 1.5 a The number of included H-bond restraints is indicated...
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Báo cáo Y học: Domain organization, folding and stability of bacteriophage T4 fibritin, a segmented coiled-coil protein docx

Báo cáo Y học: Domain organization, folding and stability of bacteriophage T4 fibritin, a segmented coiled-coil protein docx

Báo cáo khoa học

... transition 486 281 2 58 182 120 1 08 75 58 )9 280 )3610 )3170 )1660 – )1216 )630 )515 )7600 )3 080 )2640 )1170 ) 687 )656 – – – )530 )530 )490 – )560 – )515 0.13 0.39 0.42 0 .88 0.91 0 .81 – – The crystal ... coiled coil Biochemistry 34, 86 42 86 48 25 Engel, J & Kammerer, R.A (2000) What are oligomerization domains good for? Matrix Biol 19, 283 – 288 26 Cohen, C & Parry, D.A (19 98) A conserved C-terminal ... 789 –7 98 Strelkov, S.V., Tao, Y., Shneider, M.M., Mesyanzhinov, V.V & Rossmann, M.G (19 98) Structure of bacteriophage T4 fibritin M: a troublesome packing arrangement Acta Crystallogr D54, 80 5 81 6...
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Báo cáo Y học: Cytochrome c from a thermophilic bacterium has provided insights into the mechanisms of protein maturation, folding, and stability potx

Báo cáo Y học: Cytochrome c from a thermophilic bacterium has provided insights into the mechanisms of protein maturation, folding, and stability potx

Báo cáo khoa học

... (19 98) The stability of proteins in ¨ extreme environments Curr Opin Struct Biol 8, 7 38 7 48 Lee, B & Vasmatzis, G (1997) Stabilization of protein structures Curr Opin Biotechnol 8, 423–4 28 Szilagyi, ... Biochemistry 34, 81 15 81 22 Perl, D., Muller, U., Heinemann, U & Schmid, F.X (2000) Two ¨ exposed amino acid residues confer thermostability on a cold shock protein Nat Struct Biol 7, 380 – 383 Sanbongi, ... 276, 4 581 3–4 581 7 Pertinhez, T.A., Bouchard, M., Tomlinson, E.J., Wain, R., Ferguson, S.J., Dobson, C.M & Smith, L.J (2001) Amyloid fibril formation by a helical cytochrome FEBS Lett 495, 184 – 186 Tomlinson,...
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Islamic vs. Conventional Banking: Business Model, Efficiency and Stability ppt

Islamic vs. Conventional Banking: Business Model, Efficiency and Stability ppt

Ngân hàng - Tín dụng

... 1.417 13.5 28 36.726 17. 480 1.121 10.705 36 .89 8 0.271 0.000 0.000 0 .88 6 384 22 383 33 37 188 13.762 44.451 1 .88 2 1 .88 8 23.462 1.712 10.959 13.610 0.109 16 .86 6 85 .490 5.411 13.572 41.737 2. 288 13.766 ... 13.610 0.109 16 .86 6 85 .490 5.411 13.572 41.737 2. 288 13 .88 2 47.514 1.5 28 0.000 0.000 0.000 315 303 309 322 2 58 3 58 8.035 4 .87 1 0.657 47.360 0.537 14.390 1.5 28 3.252 0.190 21.111 0.424 25 .89 2 5.544 ... 0.0909* 0.0904* -0. 185 8* -0.1315* 0.0142 0.11 68* -0.20 18* 0.2472* 0.16 98* 0.4214* -0.0449* 0.20 48* -0. 187 0* -0.22 98* -0.0195 0.0 286 * -0.1 486 * 0. 087 9* 0.1 480 * 0.2102* 0.0 683 * -0.1956* -0.2904*...
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Báo cáo khoa học: Metal ions modulate the folding and stability of the tumor suppressor protein S100A2 docx

Báo cáo khoa học: Metal ions modulate the folding and stability of the tumor suppressor protein S100A2 docx

Báo cáo khoa học

... 4.7 +Zn2+ 2.5 +Ca2+ 3.9 89 .9 35.1 40.3 13.0 3.5 2.9 – )14.2 )5.2 4.5 4.0 4 .8 78. 9 50.1 62.4 11.2 5.3 7.0 – )3.9 +2.4 4.2 4.1 4.3 71 .8 68. 2 51 .8 10.3 9.7 5.3 – )0 .8 +0 .8 a DDGU = D[Urea]1 ⁄ · ... FEBS Lett 282 , 405–4 08 17 Franz C, Durussel I, Cox JA, Schafer BW & Heizmann CW (19 98) Binding of Ca2+ and Zn2+ to human nuclear S100A2 and mutant proteins J Biol Chem 273, 188 26– 188 34 18 Koch M, ... +Ca2+ (10 : 1) wt C2S 58. 4 66.6 56.6 53.9 56.6 50.6 DCys 59.5 58. 1 Aggregates 68. 1  42 > 80  75 > 85 Apo S100A2-wt and S100A2-DCys have very similar T app values of 58. 4 and 59.5 °C, respectively,...
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Báo cáo khoa học: Tryptophan 243 affects interprotein contacts, cofactor binding and stability in D-amino acid oxidase from Rhodotorula gracilis ppt

Báo cáo khoa học: Tryptophan 243 affects interprotein contacts, cofactor binding and stability in D-amino acid oxidase from Rhodotorula gracilis ppt

Báo cáo khoa học

... (nm) Flavin a.u 0.02 ± 0.01a 110 ± 8b 0 .8 ± 0.2b 12.7 0.12 ± 0.01 86 ± 1.5 ± 0.2 0.37 ± 0.03 95 ± 2d 1.6 ± 0.1d 135 940 230 900 340 465 370 715 0.04 ± 0.01 1 08 ± 1.4 ± 0.1 As described previously ... (°C) Trp fluorescence 46 .8 FAD fluorescence 47.5 ANS fluorescence 50.0 Urea Cm (M) Trp fluorescence 1.4 (1 .8) FAD fluorescencec 1 .8, 6.2 39.2 42.3 n.d 1.0 (2.0) 1.3, 5.6 42.4 38. 5 41.7 n.d (1.9) n.d ... excess of free FAD (0.2 mM) in the activity assay mixture 506 d (334) (342) (3 38) (342) (3 38) (340) (337) (341) 18. 9 9.4 12.3 These values were determined in the presence FEBS Journal 273 (2006)...
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Báo cáo khóa học: High level cell-free expression and specific labeling of integral membrane proteins doc

Báo cáo khóa học: High level cell-free expression and specific labeling of integral membrane proteins doc

Báo cáo khoa học

... inhibitorb Hepes-KOH pH 8. 0 EDTA magnesium acetate potassium acetate polyethylenglycol 80 00 sodium azide a UÆlL 500 lgÆmL 40 lgÆmL 0.5–1 mM 20 mM 20 mM 1.2 mM 0 .8 mM 0 .8 mM 0 .8 mM mM 0.2 mM tablet ... tablet per 10 mL – – – 1–1.5 mM 20 mM 20 mM 1.2 mM 0 .8 mM 0 .8 mM 0 .8 mM mM 0.2 mM tablet per 10 mL 100 mM 2 .8 mM 13 mM 290 mM 2% 0.05% 100 mM 2 .8 mM 13 mM 290 mM 2% 0.05% Amersham Biosciences b ... (1 988 ) A continuous cell-free translation system Harbor, NY 18 Zubay, G (1973) In vitro synthesis of protein in microbial systems 27 Annu Rev Genet 7, 267– 287 19 Schagger, H & Jagow, G.V (1 987 )...
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