Aqueous channels within apolar peptide aggregates. Solvated helix of Boc-Aib-Ala-Leu-Aib-Ala-Leu-Aib- -Ala-Leu-Aib-OMe. H2O.CH3OH

Although the peptide Boc-Aibl-Ala2-Leu3- Aib4-Alas Leu'-Aib7-Ala8-Leu9-Aib'0-OMe [with a t-butoxycarbonyl(Boc) blocking group at the amino terminus, a methyl ester (OMe) at the carboxyl terminus, and four a-aminoisobutyric (Aib) residues] has a 3-fold repeat of residues, the helix formed by the peptide backbone is irregular. The carboxyl-terminal half assumes an at-helical form with torsion angles ) and r of approximately -60° and -45°, respectively, whereas the amino-terminal half is distorted by an insertion of a water molecule between the amide nitrogen of Ala5 [N(5)] and the carbonyl oxygen of Ala2 [0(2)]. The water molecule W(1) acts as a bridge by forming hydrogen bonds N(5).W(1) (2.93 A) and W(1)---0(2) (2.86 A). The distortion of the helix exposes the carbonyl oxygens of Aib' and Aib4 to the outside environment, with the consequence that the helix assumes an amphiphilic character despite having all apolar residues. Neighboring helices in the crystal run in antiparallel directions. On one side of a helix there are only hydrophobic contacts with efficient interdigitation of leucine side chains with those from the neighboring helix. On the other side of the helix there are hydrogen bonds between protruding carbonyl oxygens and four water molecules that separate two neighboring helices. Along the helix axis the helices bind head-to-tail with a direct hydrogen bond N(2)-0(9) (3.00 A). Crystals grown from methanol/water solution are in space group P2, with a = 15.778 ± 0.004 A, b = 11.228 ± 0.002 A, c = 18.415 ± 0.003 A, = 102.10 ± 0.02ur and two formula units per cell for C49HON1003 2H2OCH3OH. The overall agreement factorR is 7.5% for 3394 reflections observed with intensities >3a(F), and the resolution is 0.90 A.

Reactivity Of Pph3 Toward Ruiiruiiicl(O2car)4 - Syntheses, Molecular-Structures, And Spectroscopic And Electrochemical Properties Of Ruiiruiii(Oh2)Cl(Mecn)(O2car)4(Pph3)2 And Ruii2(Oh2)(Mecn)2(O2car)4(Pph3)2

By the reaction of Ru2Cl(O2CAr)4 (1) and PPh3 in MeCN-H2O the diruthenium(II,III) and diruthenium(II) compounds of the type Ru2(OH2)Cl(MeCN)(O2CAr)4(PPh3)2 (2) and Ru2(OH2)(MeCN)2(O2CAr)4(PPh3)2 (3) were prepared and characterized by analytical, spectral, and electrochemical data (Ar is an aryl group, C6H4-p-X; X = H, OMe, Me, Cl, NO2). The molecular structure of Ru2(OH2)Cl(MeCN)(O2CC6H4-p-OMe)4(PPh3)2 was determined by X-ray crystallography. Crystal data are as follows: triclinic, P1BAR, a = 13.538 (5) angstrom, b = 15.650 (4) angstrom, c = 18.287 (7) angstrom, alpha = 101.39 (3)-degrees, beta = 105.99 (4)-degrees, gamma = 97.94 (3)-degrees, V = 3574 angstrom 3, Z = 2. The molecule is asymmetric, and the two ruthenium centers are clearly distinguishable. The Ru(III)-Ru(II), Ru(III)-(mu-OH2), and Ru(II)-(mu-OH2) distances and the Ru-(mu-OH2)-Ru angle in [{Ru(III)Cl(eta-1-O2CC6H4-p-OMe)(PPh3)}(mu-OH2)(mu-O2CC6H4-p-OMe)2{Ru(II)(MeCN)(eta-1-O2CC6H4-p-OMe)(PPh3)}] are 3.604 (1), 2.127 (8), and 2.141 (10) angstrom and 115.2 (5)-degrees, respectively. The compounds are paramagnetic and exhibit axial EPR spectra in the polycrystalline form. An intervalence transfer (IT) transition is observed in the range 900-960 nm in chloroform in these class II type trapped mixed-valence species 2. Compound 2 displays metal-centered one-electron reduction and oxidation processes near -0.4 and +0.6 V (vs SCE), respectively in CH2Cl2-TBAP. Compound 2 is unstable in solution phase and disproportionates to (mu-aquo)diruthenium(II) and (mu-oxo)diruthenium(III) complexes. The mechanistic aspects of the core conversion are discussed. The molecular structure of a diruthenium(II) compound, Ru2(OH2)(MeCN)2(O2CC6H4-p-NO2)4(PPh3)2.1.5CH2Cl2, was obtained by X-ray crystallography. The compound crystallizes in the space group P2(1)/c with a = 23.472 (6) angstrom, b = 14.303 (3) angstrom, c = 23.256 (7) angstrom, beta = 101.69 (2)-degrees, V = 7645 angstrom 3, and Z = 4. The Ru(II)-Ru(II) and two Ru(II)-(mu-OH2) distances and the Ru(II)-(mu-OH2)-Ru(II) angle in [{(PPh3)-(MeCN)(eta-1-O2CC6H4-p-NO2)Ru}2(mu-OH2)(mu-O2CC6H4-p-NO2)2] are 3.712 (1), 2.173 (9), and 2.162 (9) angstrom and 117.8 (4)-degrees, respectively. In both diruthenium(II,III) and diruthenium(II) compounds, each metal center has three facial ligands of varying pi-acidity and the aquo bridges are strongly hydrogen bonded with the eta-1-carboxylato facial ligands. The diruthenium(II) compounds are diamagnetic and exhibit characteristic H-1 NMR spectra in CDCl3. These compounds display two metal-centered one-electron oxidations near +0.3 and +1.0 V (vs SCE) in CH2Cl2-TBAP. The overall reaction between 1 and PPh3 in MeCN-H2O through the intermediacy of 2 is of the disproportionation type. The significant role of facial as well as bridging ligands in stabilizing the core structures is observed from electrochemical studies.

Interactions of tris buffer with nucleotides: the crystal structure of tris(hydroxymethyl)methylammonium adenosine 5'-diphosphate dihydrate

The crystal and molecular structures of the Tris salt of adenosine 5'-diphosphate were determined from X-ray diffraction data. The crystals are monoclinic, space P21, and Z = 2 with a=9.198 (2) A, b=6.894 (1) A, c=18.440 (4) A, and beta = 92.55 (2) degrees. Intensity data were collected on an automated diffractometer. The structure was solved by the heavy-atom technique and refined by least squares to R = 0.047. The ADP molecule adopts a folded conformation. The conformation about the glycosidic bond is anti. The conformation of the ribose ring is close to a perfect C(2')-endo-C-(3')-exo puckering. The conformation about C(4')-C(5') is gauche-gauche, similar to other nucleotide structures. The pyrophosphate chain displays a nearly eclipsed geometry when viewed down the P-P vector, unlike the staggered conformation observed in crystal structures of other pyrophosphates. The less favorable eclipsed conformation probably results from the observed association of Tris molecules with the polar diphosphate chain through electrostatic interactions and hydrogen bonds. Such interactions may play an important role in Tris-buffered aqueous solutions of nucleotides and metal ions.

Crystal structure of a daturalactone - a withanolide

The crystal structure of a daturalactone derivative has been determined by X-ray structural analysis. The compound crystallizes in orthorhomic space group P2(1)2(1)2(1) with cell parameters a = 15.141(1) angstrom, b = 18.425(1) angstrom, c = 19.251(2) angstrom. The structure was solved by direct methods and refined to R = 0.082. The asymmetric unit contains two non-equivalent molecules. Extensive hydrogen bonding is present. The conformations of the rings are A: a distorted half-chair, B: a perfect half-chair, C: a chair, D: an envelope-half chair and E: a twist boat. Ring junctions A/B, B/C, C/D are all trans fused. Methyl carbons C(18), C(19), C(27) and the lactone moiety is beta-oriented whereas the methyl carbons C(21) and C(28) are alpha-oriented.

Synthesis of Trilaurin by Developing Pisa Seeds (Actinodaphne hookeri)

The developing seeds of Actinodaphne hookeri were investigated to delineate their ability to synthesize large amounts of trilaurin. Until 88 days after flowering the embryos contained 71% neutral lipids (NL) and 29% phospholipids (PL) and both these components contained C-16:0, C-18:0, C-18:2, and C-18:3 as the major fatty acids (FA). At 102 days after flowering the seeds began to accumulate triacylglycerols (TAG) and to synthesize lauric acid (C-12:0). By 165 days after flowering, when the seeds were mature, they contained about 99% NL and 1% FL. At this stage the TAG contained exclusively C-12:0, while the PL consisted of long-chain fatty acids (LCFA) only. Leaf lipids in contrast did not contain any C-12:0. Experiments on [1-C-14]acetate incorporation into developing seed slices showed that at 88 days after flowering only 4% of the label was in TAG, 1% in diacylglycerols (DAG), and 87% in FL. One hundred two days after flowering seeds incorporated only 2% of the label into TAG, 30% into DAG, and 64% into FL. In contrast at 114 days after flowering 71% of the label was incorporated into TAG, 25% into DAG, and only 2% into FL. Analysis of labeled FA revealed that up to 102 days after flowering it was incorporated only into LCFA, whereas at 114 days after flowering it was incorporated exclusively into C-12:0. Furthermore, 67% of the label in PL at 114 days after flowering was found to be dilaurylglycerophosphate. Analysis of the label in DAG at this stage showed that it was essentially in dilaurin species. These observations indicate the induction of enzymes of Kennedy pathway for the specific synthesis of trilaurin at about 114 days after flowering, Homogenates of seeds (114 days after flowering) incubated with labeled FA in the presence of glycerol-3-phosphate and coenzymes A and ATP incorporated 84% of C-12:0 and 61% of C-14:0, but not C-16:0, C-18:2, and C-18:3, into TAG. In contrast the LCFA were incorporated preferentially into FL. It is concluded that, between 102 and 114 days after flowering, a switch occurs in A. hookeri for the synthesis of C-12:0 and trilaurin which is tissue specific. Since the seed synthesizes exclusively C-12:0 at 114 days after flowering onwards and incorporates specifically into TAG, this system appears to be ideal for identifying the enzymes responsible for medium-chain fatty acid as well as trilaurin synthesis and for exploiting them for genetic engineering. (C) 1994 Academic Press, Inc.

A new layered iron fluorophosphate

A new iron fluorophosphate of the composition, [C6N4H21] [Fe2F2(HPO4)(3)][H2PO4](.)2H(2)O, I has been prepared by the hydrothermal route. This compound contains iron fluorophosphate layers and the H2PO4- anions are present in the interlayer space along with the protonated amine and water molecules. The compound crystallizes in the monoclinic space group P2(1)/c. (a = 13-4422(10) Angstrom, b = 9 7320(10) Angstrom, c = 18-3123(3) Angstrom, beta = 92-1480degrees, V = 2393-92(5) Angstrom 3, Z = 4, M = 719-92, d(calc). = 1.997 g cm(-3), R-1 = 0.03 and wR(2) = 0,09).

Chromatographic methods for determination of nimesulide and for stability studies

Simple and rapid HPLC, GC, and TLC procedures have been developed for detection and determination of nimesulide, a non-pharmacopeial drug, in preformulation and dosage form. Use of these techniques has enabled separation of impurities and the precursor in the bulk material and in formulations. Isocratic reversed-phase HPLC was performed on a C-18 column with methanol-water-acetic acid, 67:32:1 (v/v), as mobile phase and UV detection at 230 nm. Calibration curves were linear over the concentration range 100-1000 mug mL(-1) with a good correlation coefficient (0.9993) and a coefficient of variation of 1.5%. Gas chromatography was performed on an OV-17 packed column with temperature programming and flame-ionization detection. The lower limit of determination by HPLC and GC was 4 ppm. Thin-layer chromatography of nimesulide was performed on silica gel G with toluene-ethyl acetate, 8:2, as mobile phase. Stability testing of the drug was performed under different temperature, humidity, and UV-radiation conditions.

4-(4-Chlorophenyl)-N-[(E)-4-(dimethylamino)benzylidene]-1,3-thiazol-2- amine

The title compound, C(18)H(16)ClN(3)S, adopts an extended molecular structure. The thiazole ring is inclined by 9.2 (1) and 15.3 (1)degrees with respect to the chlorophenyl and 4-(dimethylamino)phenyl rings, respectively, while the benzene ring planes make an angle of 19.0 (1)degrees. A weak intermolecular C-H center dot center dot center dot pi contact is observed in the crystal structure.

Climate change and crop yields in the Indian Cardamom Hills, 1978-2007 CE

In this study we analyzed climate and crop yields data from Indian cardamom hills for the period 1978-2007 to investigate whether there were significant changes in weather elements, and if such changes have had significant impact on the production of spices and plantation crops. Spatial and temporal variations in air temperatures (maximum and minimum), rainfall and relative humidity are evident across stations. The mean air temperature increased significantly during the last 30 years; the greatest increase and the largest significant upward trend was observed in the daily temperature. The highest increase in minimum temperature was registered for June (0.37A degrees C/18 years) at the Myladumpara station. December and January showed greater warming across the stations. Rainfall during the main monsoon months (June-September) showed a downward trend. Relative humidity showed increasing and decreasing trends, respectively, at the cardamom and tea growing tracts. The warming trend coupled with frequent wet and dry spells during the summer is likely to have a favorable effect on insect pests and disease causing organisms thereby pesticide consumption can go up both during excess rainfall and drought years. The incidence of many minor pest insects and disease pathogens has increased in the recent years of our study along with warming. Significant and slight increases in the yield of small cardamom (Elettaria cardamomum M.) and coffee (Coffea arabica), respectively, were noticed in the recent years.; however the improvement of yield in tea (Thea sinensis) and black pepper (Piper nigrum L.) has not been seen in our analysis.

Sensitive Liquid Chromatography-Tandem Mass Spectrometry Method for the Determination of Olanzapine in Human Urine

A sensitive and selective liquid chromatographic-tandem mass spectrometric (LC-MS-MS) method was developed to determine olanzapine (OLZ) in human urine. After solid-phase extraction with SPE cartridge, the urine sample was analysed on a C-18 column (Symmetry 3.5 mu m, 50 x 4.6 mm i.d) interfaced with a triple quadrupole tandem mass spectrometer. Positive electrospray ionization was employed as the ionization source. The mobile phase consisted of ammonium acetate (pH 7.8)-acetonitrile (10:90, v/v). The method was linear over a concentration range of 1-100 ngml(-1). The lower limit of quantitation was 1 ngml(-1). The intra-day and inter-day relative standard deviation across three validation runs over the entire concentration range was < 11.5 %. The accuracy determined at three concentrations (8.0, 50.0 and 85.0 ngml(-1) OLZ) was within +/- 1.21 % in terms of relative errors.

A Rodinian suture in western India: New insights on India-Madagascar correlations

We report detailed evidence for a new paleo-suture zone (the Kumta suture) on the western margin of southern India. The c. 15-km-wide, westward dipping suture zone contains garnet-biotite, fuchsite-haematite, chlorite-quartz, quartz-phengite schists, biotite augen gneiss, marble and amphibolite. The isochemical phase diagram estimations and the high-Si phengite composition of quartz-phengite schist suggest a near-peak condition of c. 18 kbar at c. 550 degrees C, followed by near-isothermal decompression. The detrital SHRIMP U-Pb zircon ages from quartz-phengite schist give four age populations ranging from 3280 to 2993 Ma. Phengite from quartz-phengite schist and biotite from garnet-biotite schist have K-Ar metamorphic ages of ca. 1326 and ca. 1385 Ma respectively. Electron microprobe-CHIME ages of in situ zircons in quartz-phengite schist (ca. 3750 Ma and ca. 1697 Ma) are consistent with the above results. The Bondla ultramafic-gabbro complex in the west of the Kumta suture compositionally represents an arc with K-Ar biotite ages from gabbro in the range 1644-1536 Ma. On the eastern side of the suture are weakly deformed and unmetamorphosed shallow westward-dipping sedimentary rocks of the Sirsi shelf, which has the following upward stratigraphy: pebbly quartzite/sandstone, turbidite, magnetite iron formation, and limestone; farther east the lower lying quartzite has an unconformable contact with ca. 2571 Ma quartzo-feldspathic gneisses of the Dharwar block with a ca. 1733 Ma biotite cooling age. To the west of the suture is a c. 60-km-wide Karwar block mainly consisting of tonalite-trondhjemite-granodiorite (TTG) and amphibolite. The TTGs have U-Pb zircon magmatic ages of ca. 3200 Ma with a rare inherited core age of ca. 3601 Ma. The K-Ar biotite cooling age from the TTGs (1746 Ma and 1796 Ma) and amphibolite (ca. 1697 Ma) represents late-stage uplift. Integration of geological, structural and geochronological data from western India and eastern Madagascar suggest diachronous ocean closure during the amalgamation of Rodinia; in the north at around ca. 1380 Ma, and a progression toward the south until ca. 750 Ma. Satellite imagery based regional structural lineaments suggests that the Betsimisaraka suture continues into western India as the Kumta suture and possibly farther south toward a suture in the Coorg area, representing in total a c. 1000 km long Rodinian suture. (C) 2013 Elsevier B.V. All rights reserved.

Estudio de pre-factibilidad de una propuesta de desarrollo ganadero para la finca "El Garabato" en Tola, Rivas

En el presente trabajo se evaluó EX-ante la factibilidad técnica y financiera de una propuesta de desarrollo ganadero para la finca "El Garabato" planteada por los socios de la Cooperativa Ezequiel N24 en el Municipio de Tola, Departamento de Rivas. Para ello se realizó un diagnóstico general de la finca, donde se determinó los recursos disponibles y las características propias del sistema productivo, basados en esto se estimaron los diferentes coeficientes técnicos así como las posibles fuentes de ingresos y egresos, permitiendo realizar las proyecciones del hato así como las proyecciones financieras, Dentro de los aspectos técnicos se determinó la composición de las pasturas donde el 69% de los pastos son naturalizados, el 23% son pastos mejorados y el 8% está conformado por pastos naturales. Los canales de comercialización en la zona del proyecto para la leche están representados por los manteros, el Proyecto Juan Agustín Guillén de la Tienda Campesina y el Centro de Acopio de La Selecta. En el caso de la carne por los intermediarios (matarifes) y productores dedicados a la crianza y engorde de novillos. Al considerar las inversiones en pastura que conlleva la propuesta, la distribución de pastos varia, ocupando los pastos mejorados el 41%, el 3% por pastos naturales y el 56% corresponden a pastos naturalizados. A la par de esto el área ganadera se incrementa en 64 mz. como consecuencia de la reducción del área agricola por la misma cantidad de mz. Las disponibilidades de pastos se ven mejoradas por las inversiones, disminuyendo el déficit de alimento a partir del segundo año. El uso de la Caña de Azúcar más urea, durante el verano permitirá mejorar la oferta de alimento para esta época, resultando menores pérdidas en la producción. Como efecto de la propuesta se producirá un incremento promedio anual de 7.18% del hato total, este incremento se da esperando que los índices de mortalidad de adultos y terneros disminuyan de un 4 al. 2% y de 14 al 7% respectivamente y que la tasa de descarte de vacas se mantenga en 12%1 considerando que la finca mantenga un 67% en tasa de natalidad. Al estructurar los gastos se encontró que en el año base los gastos de mano de obra representan el 71%, la suplementación el 8%, los gastos en manejo fueron de 8%, impuestos 7%, mantenimiento de equipo e infraestructura de 4% y gastos varios de 1%, con el proyecto esta estructura de gastos se ve un poco alterada al disminuir los gastos por mano de obra a un 63% e incrementarse los gastos por suplementacion y gastos varios a 12% y 6% respectivamente, el resto de los gastos presentan leves modificaciones. En los ingresos del año base la producción de leche representa el 46%, la producción de carne el 53% y el 1% corresponde a otros ingresos. Con el proyecto el aporte en los ingresos por producción de leche asciende a 62% y en producción de carne es de 34%, en otros ingresos representa el 4% al finalizar el sexto año. De las inversiones que se realizaran el 60% ésta destinado para pastos y el 40% corresponde a inversiones en infraestructura. El monto total de la inversión asciende a C$96,905.70 de los cuales el 71% será solicitado en préstamo y el restante 29% será asumido por la Cooperativa. Del análisis financiero resultó que la propuesta de los socios con uso de financiamiento para las inversiones a una tasa de interés del 12.5% presenta un VAN de C$41996.65 y una TIR de 15.16%. En cambió la realización de la propuesta con recursos propios presentó resultados superiores al anterior siendo el VAN de C$18,506.01 y una TIR de 18.01%•. Considerando estos resultados la propuesta es rentable, pero debido al déficit de efectivo que se presenta en los primeros años podría alterar la realización de las inversiones, ésta situación puede compensarse haciendo uso de otros recursos de la Cooperativa.

Determinación de la dosis óptima del insecticida Chlorpyrifos aplicado manualmente al cogollo para control de Spodoptera frugiperda Smith (Lepidoptera: noctuidae) en el cultivo del maiz (Zea mays L.) en la época de riego y primera

En el presente estudio se probaron 6 dosis del producto chlorpyrifos, estas fueron la siguiente: 1 1/mz. , 0.5 1/mz., 0.25 1/mz., 0.125 1/mz. 0.0625 1/mz. Y un testigo de aplicación. El propósito era determinar cuál de estas dosis seria la óptima para reducir las poblaciones del “gusano cogollero” spodoptera frugiperda Smith (lepidóptera: noctuidae). El estudio se llevó a cabo en dos épocas, en época bajo riego y en época de primera. Se evaluó también el grado de daño, componente de rendimiento propiamente dicho. En la época bajo riego, no hubo diferencia significativa entre los tratamiento en la variable del rendimiento, pero el tratamiento que brindo una mayor ganancia netya fue la dosis de 0.5 1/mz., siendo la ganancia neta de C$ 18,662.05, y el rendimiento fue de 6.77 qq/mz. (440.25 kg/ha). En la época de primera hubo diferencia significativa entre los tratamiento en lo que a rendimiento fue la dosis de 0.25 1/mz., produciendo 2.71 qq/mz. (176.24 kg/ha.). Obteniéndose C$ 6,101.18 de ganancia neta. Cabe de señalar que en la época de riego, la dosis de 0.5 1/mz. Es la que prorciona mayor ganancia neta y mayor rendimiento, pero la dosis de 1 1/mz. Proporciona 6.62 qq/mz. (430.51 kg/ha.) y una ganancia neta de C$ 18,350.85, de manera que no difiere en grandes cifras ni la ganancia neta ni los rendimiento, y al aplicar la dosis de 0.5 1/mz. Se reduce el costo de aplicación. Es importante señalar también que se reduce de manera considerable la dosis y el número de aplicaciones s, ya que en época primera. Las aplicaciones se reducen a una sola, y en época de riego no excedieron de dos. Se obtuvieron rendimiento bajo, ya que cierta forma la presión de ovoposición del “cogollero” en época de riego y las fuertes explosiones de chicharrita dulzuras mays del cero al uno %. En la época de primera. Iniciaron en gran forma al hecho de haber obtenido estos rendimientos.

Plan de negocios en las comunidades de la Laguna Negra y San Isidro del municipio de Camoapa

El presente trabajo es una investigación de campo de tipo descriptivo, documental, no experimental y se realizó según las normativas de la Universidad Nacional Agraria. En primer lugar, se realizaron las visitas a las comunidades de San Isidro y La Laguna Negra con el propósito de observar y conocer la situación socioe conómica de las familias y a la vez conseguir el involucramiento y aprobación de la población para la utilización de las casas comunales de una forma viable y su mejoramiento. Se utilizó el método matricial para elegir una idea de negocio a ejecutar y desarrollarla en ambas casas comunales, siendo electa la elaboración de un plan de negocio que incluye la venta de abarrotes, medicinas y herramientas del campo. Los resultados están basados a la estructura de un Plan de Negocios, teniendo unas compras proyectadas para el primer mes de C$ 109,867.09 y unas ventas de C$ 128,461.98 en ambas casas obteniendo una ganancia de C$ 18,594.89; con una ganancia anual de C$ 223,138.68. Para la iniciación del negocio se pretende realizar un crédito de C$ 243,796.49 con una tasa de interés del 14%, con pagos anuales; se obtuvo un valor actual neto de 82,510.62 y una tasa de interés rentable de 19.34%. Como la idea principal era la mejora de las casas comunales se ejecutó la elaboración de un presupuesto de inversión el cual asume una cantidad de C$ 112,929.40 (Ciento doce mil novecientos veinte y nueve c��rdobas con 40/100); la cual se incluirá en la inversión inicial sustentada en el financiamiento.

N49 phospholipase A(2), a unique subgroup of snake venom group II phospholipase A(2)

A novel phospholipase A(2) (PLA(2)) with Asn at its site 49 was purified from the snake venom of Protobothrops mucrosquamatus by using SP-Sephadex C25, Superdex 75, Heparin-Sepharose (FF) and HPLC reverse-phage C-18 chromatography and designated as TM-N49