scholarly journals Cadmium uptake and distribution in tomato plants (Lycopersicon esculentum Mill)

2007 ◽  
Vol 25 (1) ◽  
pp. 37 ◽  
Author(s):  
S. Cherian ◽  
V. Ramachandran ◽  
S. Sudhakaran ◽  
H. Nair
Keyword(s):  
Sodium Dodecyl ◽  
Dry Mass ◽  
Sand Culture ◽  
Growth Responses ◽  
Tomato Plants ◽  
Plant Parts ◽  
Tomato Seedlings ◽  
Low Concentrations ◽  
Sds Page ◽  
Fresh And Dry Mass

The growth responses and accumulation of heavy metal cadmium (Cd) was studied in tomato plants. Tomato seedlings were raised in sand-culture and watered with nutrient solution containing cadmium (in the form of CdCl2) at doses ranging from 0 to 7.12 mM. At low concentrations, there was no marked growth reduction in terms of fresh and dry mass. However, the highest concentration (7.12 mM) of cadmium depressed growth in terms of fresh and dry mass and caused reduction in chlorophyll content. Sodium Dodecyl Sulfate Page Gel Electrophoresis (SDS-PAGE) of proteins showed the expression of low molecular weight proteins (~18, ~30 kDa) in Cd-treated plants when compared to control. Among the different plant parts examined for Cd accumulation, the root tissue showed maximum accumulation. The uptake, distribution and possible implications of cadmium tolerance in tomato plants are discussed.

Growth of five hybrid poplar genotypes exposed to interacting elevated CO2 and O3

1998 ◽  
Vol 28 (11) ◽  
pp. 1706-1716 ◽  
Author(s):  
R E Dickson ◽  
M D Coleman ◽  
D E Riemenschneider ◽  
J G Isebrands ◽  
G D Hogan ◽  
...  
Keyword(s):  
Carbon Allocation ◽  
Negative Impact ◽  
Hybrid Poplar ◽  
Control Plant ◽  
Basal Area ◽  
Dry Mass ◽  
Atmospheric Pollutants ◽  
Growth Strategies ◽  
Growth Responses ◽  
Plant Parts

A wide variety of hybrid poplar clones are being introduced for intensive culture biomass production, but the potential clonal or genotypic response to increasing tropospheric carbon dioxide (CO2), ozone (O3), and their interactions are unknown. To study these effects, we exposed five different hybrid Populus clones to increased concentrations of CO2, O3, and CO2 + O3 in open-top chambers for one growing season and determined growth responses. Exposure to elevated CO2 increased height growth, dry mass, and basal area; exposure to O3 decreased all three of these growth responses. Exposure impact differed among the different plant parts (leaf, stem, and roots) and among the clones. These differences were associated with different growth strategies or carbon allocation patterns inherent in the different clones. The fastest growing clones had the greatest response to O3 treatment. The addition of CO2 to the O3 exposure counteracted the negative impact of O3 in all plant components except leaf mass (e.g., CO2 + O3 plant mass equaled control plant mass) in all of the clones. But correspondingly, added O3 negated increased growth from CO2. Genetic variation in response to atmospheric pollutants must be considered even in closely related genotypes found in Populus culture.

Effects of ACC deaminase containing rhizobacteria on plant growth and expression of Toc GTPases in tomato (Solanum lycopersicum) under salt stress

Botany ◽  
2014 ◽  
Vol 92 (11) ◽  
pp. 775-781 ◽  
Author(s):  
Jianmin Yan ◽  
Matthew D. Smith ◽  
Bernard R. Glick ◽  
Yan Liang
Keyword(s):  
Plant Growth ◽  
Solanum Lycopersicum ◽  
Protein Import ◽  
Chlorophyll Concentration ◽  
Plant Stress ◽  
Acc Deaminase ◽  
Dry Mass ◽  
Shoot Length ◽  
Tomato Seedlings ◽  
Fresh And Dry Mass

The bacterial enzyme 1-aminocyclopropane-1-carboxylate (ACC) deaminase plays a key role in lowering plant stress ethylene levels, thereby stimulating plant growth. The present study aims to evaluate whether the ACC deaminase producing plant growth promoting rhizobacterium (PGPR) Pseudomonas putida UW4 can maintain and promote plant growth in saline environments and modulate the expression of chloroplast import apparatus genes in salt-treated tomato plants (Solanum lycopersicum L.). Tomatoes were grown in the presence and absence of the PGPR and shoot length, fresh and dry mass, and chlorophyll concentration were measured after 6 weeks. The expression levels of the Toc GTPases of the chloroplast protein import apparatus were measured using quantitative real-time PCR. The results showed that the rhizobacteria significantly increased shoot length, shoot fresh and dry mass, and the chlorophyll concentration of tomato seedlings grown in the presence of up to 90 mmol·L–1 NaCl. Analysis showed that the expression of most of the Toc GTPase genes was upregulated in tomato seedlings after 6 weeks of exposure to NaCl, which may help facilitate the import into chloroplasts of proteins that are involved in the stress response.

Heterozygous Abnormal Fibrinogen Osaka III with the Replacement of γ Arginine-275 by Histidine Has an Apparently Higher Molecular Weight γ-Chain Variant

1992 ◽  
Vol 68 (05) ◽  
pp. 534-538 ◽  
Author(s):  
Nobuhiko Yoshida ◽  
Shingi Imaoka ◽  
Hajime Hirata ◽  
Michio Matsuda ◽  
Shinji Asakura
Keyword(s):  
Molecular Weight ◽  
Sodium Dodecyl Sulfate ◽  
Gel Electrophoresis ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Tetraacetic Acid ◽  
Fibrin Monomer ◽  
Sds Page ◽  
Thrombotic Tendency ◽  
Chain Variant

SummaryCongenitally abnormal fibrinogen Osaka III with the replacement of γ Arg-275 by His was found in a 38-year-old female with no bleeding or thrombotic tendency. Release of fibrinopeptide(s) by thrombin or reptilase was normal, but her thrombin or reptilase time in the absence of calcium was markedly prolonged and the polymerization of preformed fibrin monomer which was prepared by the treatment of fibrinogen with thrombin or reptilase was also markedly defective. Propositus' fibrinogen had normal crosslinking abilities of α- and γ-chains. Analysis of fibrinogen chains on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) in the system of Laemmli only revealed the presence of abnormal γ-chain with an apparently higher molecular weight, the presence of which was more clearly detected with SDS-PAGE of fibrin monomer obtained by thrombin treatment. Purified fragment D1 of fibrinogen Osaka III also seemed to contain an apparently higher molecular weight fragment D1 γ remnant on Laemmli gels, which was digested faster than the normal control by plasmin in the presence of [ethy-lenebis(oxyethylenenitrilo)]tetraacetic acid (EGTA).

Identifikasi Daging Tikus Pada Produk Baso Dengan Metode Sodium Dodecyl Sulphate Polyacrylamide Gel Electrophoresis (SDS-PAGE)

2018 ◽  
Vol 26 (2) ◽  
pp. 058
Author(s):  
Anna P. Roswiem ◽  
Triayu Septiani
Keyword(s):  
Sodium Dodecyl Sulphate ◽  
Gel Electrophoresis ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Polyacrylamide Gel ◽  
Sds Page

<em>Bahan<strong> </strong>baku untuk membuat baso adalah daging hewan, pada umumnya dari daging sapi, ayam, ikan dan babi. Di beberapa daerah di Indonesia terjadi kasus baso tikus. Tujuan penelitian ini adalah menguji ada tidaknya kandungan daging tikus pada produk baso yang dijual di pasar Cempaka Putih-Kecamatan Kramat Jakarta Pusat dan di pedagang baso atau mie baso di sekitar kampus Universitas YARSI Jakarta. Daging adalah protein salah satu metode untuk mengidentifikasi protein adalah metode Sodium Dodecyl Sulphate Polyacrylamide Gel Electrophoresis (SDS-PAGE).<strong> </strong>Hasil penelitian menunjukkan bahwa dari 6 sampel baso terindikasi ada 2 sampel baso dengan nomor 1 dan 5 yang dibuat dari campuran daging sapi dan tikus; ada 1 sampel baso dengan nomor 6 yang terbuat dari daging tikus; dan 2 sampel baso dengan nomor 2 dan 3 yang terbuat dari campuran sapi  dan babi, dan hanya 1 sampel baso dengan nomor sampel 4 yang benar-benar terbuat dari daging sapi.</em>

XYLANASE, AN ENVIRONMENTALLY FRIENDLY BLEACHING AGENT FOR PULP AND PAPER: Characterization And Stabilization Study Of Bacillus licheniformis I-5 CRUDE Xylanase

2018 ◽  
Vol 7 (3) ◽  
Author(s):  
Budiasih Wahyuntari., dkk
Keyword(s):  
Thermal Stability ◽  
Bacillus Licheniformis ◽  
Hot Spring ◽  
Sodium Dodecyl ◽  
Luria Broth ◽  
Crude Enzyme ◽  
Half Time ◽  
Triton X100 ◽  
Sds Page ◽  
Xylanolytic Enzymes

Isolate I-5 was isolated from Ciseeng hot spring, West Java and was identified as Bacillus licheniformis I-5. The isolate produces extracellular xylanolytic enzymes on Oatspelt containing Luria broth agar medium. Optimal activity of the crude enzyme was  observed at 50ºC and pH 7. The effect of sodium dodecyl sulphate, b-mercaptoethanol and Triton-X100 were observed. Incubating the crude enzyme in 1.5% SDS and 1.5% b-mercaptoethanol at 50oC for 90 minutes then adding Triton-X100 at final concentration of 3.5% for 45 minutes only reduced 5.75% of the initial enzyme activity. SDS/PAGE and zymogram analysis showed that at least two xylanolytic enzymes presence in the crude enzyme. The molecular weight of the enzyme was estimated about 127 and 20kD. The enzyme hydrolysed xylan into xylobiose, xylotriose and other longer xylooligosaccharides. Thermal stability of the crude enzyme was observed at 50, 60, and 70oC and pH 7 and 8. The results showed that the half time of the crude enzyme incubated at 50, 60, and 70oC pH 7 was 2 hours 55 minutes; 2 hours 33 minutes and 1 hour 15 minutes respectively. The half time at 50, 60 and 70oC, pH 8 was 2 hours 48 minutes; 1 hour 22 minutes and 1 hour 9 minutes respectively.keywords: Xilanase, Bacillus licheniformis I-5, thermal stability

Plastic Mulch Color Effects on Light Micro-environment and Watermelon Plant Growth

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 474d-474
Author(s):  
N.K. Damayanthi Ranwala ◽  
Dennis R. Decoteau
Keyword(s):  
Plant Growth ◽  
Light Transmission ◽  
Root Zone ◽  
Dry Mass ◽  
Plant Responses ◽  
Plastic Mulch ◽  
Plant Parts ◽  
Reflected Light ◽  
Total Light ◽  
Dry Mass Partitioning

This study was conducted to evaluate the spectral properties of various colored plastic color mulches and to determine the effects of upwardly reflected light from the mulch surfaces on watermelon plant growth when differences in root zone temperatures are minimized. Two-week-old watermelon plants were grown with black mulch, red-painted mulch, SRM-Red mulch (Sonoco, Inc., Harstville, S.C.), and white mulch. Total light reflection (58 μmol·m–2·s–1 in 400–700 nm) and red: far-red (R:FR = 0.44) of reflected light were lower in black mulch and highest in white mulch (634 and 0.92, respectively). Both black mulch and white mulch had same blue:red (B:R = 0.6) while white mulch had higher B:FR (0.58) in reflected light compared to black mulch (0.26). Reflective properties of red mulches were somewhat similar, and R:FR, B:R, and B:FR were 0.8, 0.2, and 0.18, respectively. However, SRM-Red mulch had highest total light (355 μmol·m–2·s–1 in 400–700 nm) transmission through the mulch, and R:FR, B:R, and B:FR were 0.84, 0.28, and 0.23, respectively. Light transmission through the other mulches was nonsignificant. Watermelon plants grown with black mulch and red mulches had higher internode lengths compared to white mulch after 20 days. Further, plants grown under black had significant higher petiole elongation accompanied with higher dry mass partitioning to petioles, and lower partitioning to roots, stems, and leaves. There was no effects of surface mulch color on total plant dry mass or photosynthesis although plants with black had higher transpiration rate. This suggests the differential regulation of dry mass partitioning among plant parts due to mulch color. The similar plant responses with black mulch and white mulch to plants treated with FR or R light at the end of photoperiod implies the involvement of phytochrome regulation of growth due to mulch surface color.

Majra Honey Abrogated the Normal and Cancer Cells Proliferation Inhibition by Juniperus procera Extract and Extract/Honey Generated AgNPs

2020 ◽  
Vol 20 (8) ◽  
pp. 970-981
Author(s):  
Hamed A. Ghramh ◽  
Essam H. Ibrahim ◽  
Mona Kilnay
Keyword(s):  
Anticancer Activity ◽  
Cancer Cells ◽  
Biological Activities ◽  
Sugar Content ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Bioactive Molecules ◽  
Sds Page ◽  
Splenic Cells ◽  
Juniperus Procera

Background: Juniperus procera and Majra honey are well-known as a folk medicine in many countries. Objectives: This work aimed to study the immunomodulatory effects after mixing Majra honey, J. procera water leaves extract and silver Nanoparticles (AgNPs) on immune or cancer cells. Methods: Juniperus procera water leaves extract and 20% Majra honey were prepared. Both the extract and honey were used separately to synthesize AgNPs. AgNPs were characterized using UV/Vis spectrophotometry and electron microscopy. Bioactive molecules in honey and the extract were explored using Fourier Transform Infrared (FT-IR) spectroscopy. Protein profile of honey was explored using Sodium Dodecyl Sulfate- Polyacrylamide Gel Electrophoresis (SDS-PAGE) and honey sugar content was determined using High- Performance Liquid Chromatography (HPLC). Biological activities of honey and the extract were tested. Results: The results demonstrated the ability of the extract/honey to produce AgNPs in a spherical shape. The extract/honey contained many functional groups. SDS-PAGE of Majra honey showed many protein bands. HPLC revealed honey is of good quality and no external additives are added to it. The extract and extract+ AgNPs inhibited the growth of normal rat splenic cells while honey stimulated it. The extract+honey turned stimulatory to the splenic cells’ growth and significantly diminished the inhibitory potential of the extract containing AgNPs. Both the extract and honey have antimicrobial activities, this potential increased in the presence of AgNPs. Honey and Honey+AgNPs inhibited HepG2 cancer cell proliferation while Hela cell growth inhibited only with honey+AgNPs. Conclusion: Both honey and the extract have antibacterial and immunomodulatory potentials as well as the power to produce AgNPs. Majra honey alone showed anticancer activity against HepGe2 cells, but not against Hela cells, and when contained AgNPs had anticancer activity on both cell lines. Mixing of Majra honey with J. procera extract showed characterized immunomodulatory potentials that can be described as immunostimulant.

scholarly journals Study on cocoonase, sericin, and degumming of silk cocoon: computational and experimental

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Preeti Anand ◽  
Jay Prakash Pandey ◽  
Dev Mani Pandey
Keyword(s):  
San Francisco ◽  
Tertiary Structure ◽  
Polyacrylamide Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Evolutionary Genetics ◽  
Imaging Analysis ◽  
Silk Cocoon ◽  
Natural Color ◽  
Sds Page

Abstract Background Cocoonase is a proteolytic enzyme that helps in dissolving the silk cocoon shell and exit of silk moth. Chemicals like anhydrous Na2CO3, Marseille soap, soda, ethylene diamine and tartaric acid-based degumming of silk cocoon shell have been in practice. During this process, solubility of sericin protein increased resulting in the release of sericin from the fibroin protein of the silk. However, this process diminishes natural color and softness of the silk. Cocoonase enzyme digests the sericin protein of silk at the anterior portion of the cocoon without disturbing the silk fibroin. However, no thorough characterization of cocoonase and sericin protein as well as imaging analysis of chemical- and enzyme-treated silk sheets has been carried out so far. Therefore, present study aimed for detailed characterization of cocoonase and sericin proteins, phylogenetic analysis, secondary and tertiary structure prediction, and computational validation as well as their interaction with other proteins. Further, identification of tasar silkworm (Antheraea mylitta) pupa stage for cocoonase collection, its purification and effect on silk sheet degumming, scanning electron microscope (SEM)-based comparison of chemical- and enzyme-treated cocoon sheets, and its optical coherence tomography (OCT)-based imaging analysis have been investigated. Various computational tools like Molecular Evolutionary Genetics Analysis (MEGA) X and Figtree, Iterative Threading Assembly Refinement (I-TASSER), self-optimized predicted method with alignment (SOPMA), PROCHECK, University of California, San Francisco (UCSF) Chimera, and Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) were used for characterization of cocoonase and sericin proteins. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), protein purification using Sephadex G 25-column, degumming of cocoon sheet using cocoonase enzyme and chemical Na2CO3, and SEM and OCT analysis of degummed cocoon sheet were performed. Results Predicted normalized B-factors of cocoonase and sericin with respect to α and β regions showed that these regions are structurally more stable in cocoonase while less stable in sericin. Conserved domain analysis revealed that B. mori cocoonase contains a trypsin-like serine protease with active site range 45 to 180 query sequences while substrate binding site from 175 to 200 query sequences. SDS-PAGE analysis of cocoonase indicated its molecular weight of 25–26 kDa. Na2CO3 treatment showed more degumming effect (i.e., cocoon sheet weight loss) as compared to degumming with cocoonase. However, cocoonase-treated silk cocoon sheet holds the natural color of tasar silk, smoothness, and luster compared with the cocoon sheet treated with Na2CO3. SEM-based analysis showed the noticeable variation on the surface of silk fiber treated with cocoonase and Na2CO3. OCT analysis also exemplified the variations in the cross-sectional view of the cocoonase and Na2CO3-treated silk sheets. Conclusions Present study enlightens on the detailed characteristics of cocoonase and sericin proteins, comparative degumming activity, and image analysis of cocoonase enzyme and Na2CO3 chemical-treated silk sheets. Obtained findings illustrated about use of cocoonase enzyme in the degumming of silk cocoon at larger scale that will be a boon to the silk industry.

scholarly journals The mechanism of in vitro clot lysis induced by vascular plasminogen activator

Blood ◽  
1984 ◽  
Vol 63 (6) ◽  
pp. 1331-1337 ◽  
Author(s):  
C Tran-Thang ◽  
EK Kruithof ◽  
F Bachmann
Keyword(s):  
Plasminogen Activator ◽  
Whole Blood ◽  
Apparent Molecular Weight ◽  
Clot Lysis ◽  
Initial Concentration ◽  
Low Concentrations ◽  
Sds Page ◽  
Tissue Plasminogen ◽  
Low Rate

Abstract The contribution of vascular plasminogen activator (v-PA) to the lysis of whole blood and plasma clots was investigated. v-PA released into the circulation after infusion of deamino-D-arginine vasopressin (DDAVP) was shown to bind quantitatively to plasma clots. Its apparent molecular weight, determined by the SDS-PAGE fibrin-agarose underlay method, was approximately 68,000 daltons, and its activity was quenched by antibodies against human tissue plasminogen activator (t-PA). Clots prepared from post-DDAVP plasma or post-DDAVP whole blood, rich in v- PA, did not lyse when incubated in imidazole buffer or normal plasma, as determined by the release of 125I from radiolabeled clots. However, clots made of v-PA-poor plasma or whole blood, incubated in v-PA-rich plasma, underwent substantial lysis. The concentration of PA in clots incubated in v-PA-rich plasma progressively increased in relation to the initial concentration of v-PA in the surrounding plasma. The results suggest that, at low concentrations of circulating v-PA, a hemostatic plug will lyse at a very low rate. However, when the v-PA concentration in the clot environment is increased, v-PA will accumulate progressively onto fibrin and induce thrombolysis.

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