RESUMEN
Pb hyper-accumulated Carex putuoshan was taken as experimental material and subjected to combined stress of Pb and Zn. The differential expression of proteins in their roots were analyzed by Proteomic Approach. The protein that was directly involved in the cellular defense under the Pb and Zn combined stress was separated, and expression of those genes was analyzed with Carex Evergold as control. The results were obtained by MALDI-TOF/MS analysis. After applying Pb and Zn combined stress, the expression of 9 protein spots (including 7 different proteins, 2 identical proteins, 1 unknown protein) in Carex putuoshan root was found to be significantly up-regulated. Five proteins were obtained from the 9 proteins related to carbohydrate metabolism, including malate dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, frutose-1,6-bisphosphate aldolase, enolase, and 6- phosphogluconate dehydrogenase. Two proteins were related to protein biosynthesis, including isoflavone reductase and phytochelatin synthase (PCS). From these proteins, the most important protein is PCS, which is a key enzyme in the synthesis of phytochelatins (PCs) and plays an important role in chelation. It is directly involved in cellular defense under Pb and Zn stress. After Pb and Zn combined stress, the CpPCS in Carex putuoshan was cloned. The full length of cDNA is 1461 bps, and it encodes 486 amino acids with molecular weight of 53.86 kD and pI value of 6.12. Two typical phytochelatin synthase subfamily domains constitute CpPCS protein, which includes three adjacent Cys-Cys elements in the C-terminal region. Phylogenetic analysis of PCS proteins from different species showed that it had the closest relationship with the Oryza sativa and Triticum aestivum. Real-time quantitative PCR analysis indicated that CpPCS and CePCS (Carex Evergold) genes were expressed in the root. The CpPCS and CePCS genes were up-regulated by Pb and Zn treatments. The expression of CpPCS was higher than that of CePCS under the same condition. The study found that CpPCS expression was increased by Pb and Zn stress in the Carex putuoshan enrichment process of Pb, which lead to high expression of PCS protein. CpPCS improved the accumulation ability and resistance of Carex putuoshan to heavy metals with the expression level of glucose metabolism related proteins increasing after Pb and Zn stress.
Asunto(s)
Carex (Planta)/efectos de los fármacos , Plomo/toxicidad , Raíces de Plantas/efectos de los fármacos , Estrés Fisiológico/efectos de los fármacos , Zinc/toxicidad , Carex (Planta)/metabolismo , Modelos Moleculares , Proteínas de Plantas/análisis , Proteínas de Plantas/metabolismo , Raíces de Plantas/metabolismo , Reacción en Cadena de la Polimerasa , Conformación ProteicaRESUMEN
CouR from Rhodopseudomonas palustris is a member of the MarR transcriptional regulator family. It regulates the expression of CouA and CouB, enzymes that are involved in the degradation of p-coumarate. In vivo, CouR binds to a DNA fragment containing the couAB promoter and suppresses the expression of CouA and CouB, while binding of p-coumaroyl-CoA attenuates its affinity towards DNA and activates the expression of CouA and CouB. Here, the crystallization and X-ray diffraction analyses of CouR alone and in complex with p-coumaroyl-CoA are reported. Apo and ligand-complexed CouR crystals diffracted to 2.5 and 3.3 Å resolution, respectively. The crystals of apo CouR belonged to space group P22121, with unit-cell parameters a = 62.78, b = 76.15, c = 87.38 Å, whereas the crystals of the CouR-ligand complex belonged to space group P212121, with unit-cell parameters a = 61.37, b = 69.82, c = 70.32 Å. The crystals were predicted to contain two CouR molecules or CouR-ligand complexes per asymmetric unit.
Asunto(s)
Proteínas Bacterianas/biosíntesis , Proteínas Bacterianas/genética , Clonación Molecular/métodos , Regulación Bacteriana de la Expresión Génica , Rhodopseudomonas/genética , Acilcoenzima A/biosíntesis , Acilcoenzima A/química , Acilcoenzima A/genética , Secuencia de Aminoácidos , Proteínas Bacterianas/química , Secuencia de Bases , Ácidos Cumáricos/química , Cristalización , Cristalografía por Rayos X , Datos de Secuencia Molecular , Propionatos , Rhodopseudomonas/metabolismoAsunto(s)
Antituberculosos/química , Proteínas Bacterianas/química , Carbapenémicos/química , Mycobacterium tuberculosis/enzimología , Peptidil Transferasas/química , Tienamicinas/química , Sustitución de Aminoácidos , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Sitios de Unión , Carbapenémicos/metabolismo , Dominio Catalítico , Cristalografía por Rayos X , Meropenem , Peptidil Transferasas/genética , Peptidil Transferasas/metabolismo , Tienamicinas/metabolismoRESUMEN
OBJECTIVE: To assess the efficacy and safety of azosemide in patients with edema and ascites. METHODS: A multicentral, randomized, double-blind, controlled clinical trial was applied. All 223 patients (cardiac edema 92, hepatogenic edema 63, renal edema 68) were randomized to azoesmide and furosemide group, and all patients were treated for 2 weeks. Patients with cardiac or renal edema took azosemide (30 mg/d) or furosemide (20 mg/d); patients with hepatogenic edema took azosemide (60 mg/d) or furosemide (40 mg/d). The dosage were adjusted to azosemide 60 mg/d (cardiac, renal edema), 90 mg (hepatogeic edema); or furosemide 40 mg/d (cardiac, renal edema), 60 mg (hepatogeic edema), if diuretic effects were not obtained at the end of third day. RESULTS: At the end of the study, the weight changes were (2.87+/-3.10) kg and (2.81 +/-2.84) kg; the total effective rate of edema lessen was 89.19% and 89.81%; the total effective rate of heart function improvement was 64.44% and 66.66%; the 24 h urine output increased (321.85 +/-669.52) ml and (273.80 +/-645.72) ml for azosemide and furosemide, respectively. The total effective rate of ascites lessen (tested by B-ultrasound) was 89.28% and 86.66%; abdominal girth decreased (5.20 +/-3.58) cm and (5.03 +/-3.74) cm for azosemide and furosemide, respectively. The adverse event rate was 23.01% in azosemide group and 21.01% in furosemide group; the main adverse effects were hypokalemia, hyperuricemia, hypertriglyceridemia and thirsty. CONCLUSION: Azosemide could effectively lessen edema, improve heart function and decrease ascitesûit is well tolerated and is particularly useful for the diuretic treatment.
Asunto(s)
Ascitis/tratamiento farmacológico , Diuréticos/uso terapéutico , Edema/tratamiento farmacológico , Sulfanilamidas/uso terapéutico , Adolescente , Adulto , Anciano , Ascitis/etiología , Diuréticos/efectos adversos , Método Doble Ciego , Edema/etiología , Edema Cardíaco/tratamiento farmacológico , Edema Cardíaco/etiología , Femenino , Insuficiencia Cardíaca/complicaciones , Humanos , Enfermedades Renales/complicaciones , Cirrosis Hepática/complicaciones , Masculino , Persona de Mediana Edad , Sulfanilamidas/efectos adversosRESUMEN
A plant antifungal protein, Gastrodia antifungal protein (GAFP-1) has been isolated from terminal corms of the orchid Gastrodia elata B1 f. elata, purified to homogeneity and crystallized by means of the hanging-drop vapour-diffusion method. The best quality crystals grew over several months at 277 K. The crystal used for data collection belongs to the space group P2(1)2(1)2, with unit-cell parameters a = 61.087, b = 91.488, c = 81.132 A. Using a synchrotron-radiation source, the resolution limit of the data reached 2.0 A, with an overall R(merge) of 0.097 and a completeness of 99.8%. Four independent molecules were estimated to be present in the asymmetric unit, with a solvent content of 46.3%. This data will help to solve the first structure of a monomeric monocot mannose-binding lectin.
Asunto(s)
Antifúngicos/química , Gastrodia/química , Lectinas de Unión a Manosa/química , Secuencia de Aminoácidos , Antifúngicos/aislamiento & purificación , Cristalización , Cristalografía por Rayos X/métodos , Lectinas de Unión a Manosa/aislamiento & purificación , Lectinas de Unión a Manosa/farmacología , Pruebas de Sensibilidad Microbiana , Datos de Secuencia Molecular , Proteínas de Plantas/química , Proteínas de Plantas/aislamiento & purificación , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Trichoderma/efectos de los fármacosRESUMEN
Respiratory motion during acquisition of first-pass myocardial perfusion images results in translation, distortion from out-of-plane motion, and changes in left ventricular geometry. Together these effects make visual image analysis more difficult and limit methods of quantitative analysis of contrast kinetics. We present a fully automated registration and warping algorithm for correcting translation and geometric distortions using a statistically based image registration method. Twelve patients (mean age 51 +/- 12 years) were studied 3 +/- 1 days after reperfused first myocardial infarction. Perfusion images were acquired during bolus administration of nonionic Gd-DTPA. Pixel intensity statistics were computed for each image in the neighborhood of high spatial frequencies. These statistics were then used to register and warp each target image (image to be registered and warped) to a common template image. Average image-to-image vertical translation was 2.6 +/- 0.8 pixels (3.4 +/- 1.0 mm) prior to processing and 0.9 +/- 0.3 pixels (1.2 +/- 0.4 mm) post-processing (P < 0.0001). Mean image-to-image horizontal translation was 1.7 +/- 1.2 pixels (1.8 +/- 1.2 mm) before and 1.3 +/- 0.7 pixels (1.4 +/- 0.7 mm) after processing (P = 0.05). Left ventricular endocardial area varied an average of 105 +/- 55 pixels (140.7 +/- 53.7 mm2) between images prior to processing vs. 51 +/- 15 pixels (68.3 +/- 20.1 mm2) after processing (P < 0.001). Thus automated, statistically based registration and warping of perfusion images is effective in reducing image-to-image translation. This method may permit more sensitive qualitative and quantitative evaluation of myocardial contrast-enhanced first-pass images.