Spontaneous vegetative propagules differentiation in Bowdichia virgilioides seedlings maintained at MS basal medium

An aliquot from a continuous fermenter culture of baby hamster kidney cells (BHK-21 Clone PD-4) (Wistar) maintained in Ca free Eagle's Basal Medium containing 2% Kaolin adsorbed fetal calf serum was planted in spinner flasks at 300,000 cells per ml, total volume 600 ml. After equilibration for one day at 35°C to insure that cells were in log phase, the culture was infected with the M-33-AGMK25 BHK-219 strain of rubella at an input multiplicity of about 6 TCID50 per cell. The virus was identified with specific rubella antiserum.Preliminary experiments had shown that such cultures would reach a peak or plateau HA titer of approximately 1:64, 24 hrs after inoculation and would continue to yield virus for 6 to 12 days. One hundred ml aliquot harvests were withdrawn daily and the culture was returned to volume with growth medium and incubation continued. The harvested cells were spun down rapidly at 2500 rpm per 15 mins., fixed in 3.7% gluteraldehyde in Ca free phosphate buffer saline, and post fixed in osmium tetraoxide. After dehydration, the cells were embedded in Epon 812 and cured approximately 20 hrs at 60°C.

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Somatic Embryogenesis and In vitro Plant Regeneration in Vigna trilobata (L.) Verd. - A Potential Pasture Legume

Plant Tissue Culture and Biotechnology ◽

10.3329/ptcb.v19i1.4990 ◽

1970 ◽

Vol 19 (1) ◽

pp. 89-99

Author(s):

K. Choudhary ◽

M. Singh ◽

M. S. Rathore ◽

N. S. Shekhawat

Keyword(s):

Somatic Embryogenesis ◽

Growth Regulators ◽

Somatic Embryos ◽

Basal Medium ◽

Long Term Study ◽

Continuous Application ◽

First Time ◽

Pasture Legume

This long term study demonstrates for the first time that it is possible to propagate embryogenic Vigna trilobata and to subsequently initiate the differentiation of embryos into complete plantlets. Initiation of callus was possible on 2,4-D. Somatic embryos differentiated on modified MS basal nutrient medium with 1.0 mg/l of 2,4-D and 0.5 mg/l of Kn. Sustained cell division resulted in globular and heart shape stages of somatic embryos. Transfer of embryos on to a fresh modified MS basal medium with 0.5 mg/l of Kn and 0.5 mg/l of GA3 helped them to attain maturation and germination. However, the propagation of cells, as well as the differentiation of embryos, were inhibited by a continuous application of these growth regulators. For this reason, a long period on medium lacking these growth regulators was necessary before the differentiation of embryos occurred again. The consequences for improving the propagation of embryogenic cultures in Vigna species are discussed. Key words: Pasture legume, Vigna trilobata, Globular, Heart shape, somatic embryogenesis D.O.I. 10.3329/ptcb.v19i1.4990 Plant Tissue Cult. & Biotech. 19(1): 89-99, 2009 (June)

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STUDY AND CHARACTERIZATION GROWTH OF FOUR MICROALGAE SPECIES AND TEST ANTIMICROBIAL ACTIVITY

Jurnal Zarah ◽

10.31629/zarah.v6i2.625 ◽

2018 ◽

Vol 6 (2) ◽

pp. 53-58

Author(s):

Marniati Salim

Keyword(s):

Dunaliella Salina ◽

Methanol Extract ◽

Sea Water ◽

Basal Medium ◽

Nannochloropsis Oculata ◽

Inhibitory Zone ◽

Antimicrobial Sensitivity ◽

Sensitivity Tests ◽

Microalgae Biomass ◽

Chaetoceros Calcitrans

Abstract In this study to the growth characteristics of microalgae (Dunaliella salina, Nannochloropsis oculata, Tetrasel mis chuii & Chaetoceros calcitrans), in different mediums, namely Bold’s Basal Medium (BBM) and BBM modification of sea water. The results obtained from microalgae (N.oculata, T.chuii, C.calcitrans) are better grown on BBM media while microlaga D.salina grows well on BBM modification of sea water. Microalgae biomass is extracted by maceration method in hexane and methanol solvents. Test bacteria used gram positive (Staphylococcus aureus) and gram negative (Escherichia coli). Inhibitory zone diameter results were compared with antimicrobial sensitivity tests according to Clinical and Laboratory Standards Institute (CLSI). From the results of microalgae hexane and methanol extract antibacterial activity tests (D.salina, N.oculata, T.chuii, C.calcitrans) showed that the extract was not too sensitive to inhibit bacterial growth. Keywords: microalgae, medium, antimicrobial

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Biotransformation of nitrocellulose under methanogenic conditions

Water Science & Technology ◽

10.2166/wst.1996.0567 ◽

1996 ◽

Vol 34 (5-6) ◽

pp. 327-334 ◽

Cited By ~ 2

Author(s):

David L. Freedman ◽

Bryan M. Caenepeel ◽

Byung J. Kim

Keyword(s):

Biological Treatment ◽

Enrichment Culture ◽

Basal Medium ◽

Anaerobic Biodegradation ◽

Anaerobic Treatment ◽

Acid Digestion ◽

Energetic Compounds ◽

Nitrate Ester ◽

Digestion Technique ◽

Aerobic And Anaerobic

Treatment of wastewater containing nitrocellulose (NC) fines is a significant hazardous waste problem currently facing manufacturers of energetic compounds. Previous studies have ruled out the use of biological treatment, since NC has appeared to be resistant to aerobic and anaerobic biodegradation. The objective of this study was to examine NC biotransformation in a mixed methanogenic enrichment culture. A modified cold-acid digestion technique was used to measure the percentage of oxidized nitrogen (N) remaining on the NC. After 11 days of incubation in cultures amended with NC (10 g/L) and methanol (9.9 mM), the % N (w/w) on the NC decreased from 13.3% to 10.1%. The presence of NC also caused a 16% reduction in methane output. Assuming the nitrate ester on NC was reduced to N2, the decrease in CH4 represented almost exactly the amount of reducing equivalents needed for the observed decrease in oxidized N. An increase in the heat of combustion of the transformed NC correlated with the decrease in % N. There was no statistically significant decrease in % N when only NC was added to the culture, or in controls that contained only the sulfide-reduced basal medium. The biotransformed NC has a % N comparable to nonexplosive nitrated celluloses, suggesting that anaerobic treatment may be a technically feasible process for rendering NC nonhazardous.

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Aquatic Toxicity of Photocatalyst Nanoparticles to Green Microalgae Chlorella vulgaris

Water ◽

10.3390/w13010077 ◽

2020 ◽

Vol 13 (1) ◽

pp. 77

Author(s):

Cristina Adochite ◽

Luminita Andronic

Keyword(s):

Chlorella Vulgaris ◽

Advanced Oxidation Process ◽

Growth Parameters ◽

Aquatic Toxicity ◽

Basal Medium ◽

Inhibitory Effect ◽

Synthesis Methods ◽

Potent Inhibitory Effect ◽

Density Surface ◽

The Impact

In the last years, nanoparticles such as TiO2, ZnO, NiO, CuO and Fe2O3 were mainly used in wastewater applications. In addition to the positive aspects concerning using nanoparticles in the advanced oxidation process of wastewater containing pollutants, the impact of these nanoparticles on the environment must also be investigated. The toxicity of nanoparticles is generally investigated by the nanomaterials’ effect on green algae, especially on Chlorella vulgaris. In this review, several aspects are reviewed: the Chlorella vulgaris culture monitoring and growth parameters, the effect of different nanoparticles on Chlorella vulgaris, the toxicity of photocatalyst nanoparticles, and the mechanism of photocatalyst during oxidative stress on the photosynthetic mechanism of Chlorella vulgaris. The Bold basal medium (BBM) is generally recognized as an excellent standard cultivation medium for Chlorella vulgaris in the known environmental conditions such as temperature in the range 20–30 °C and light intensity of around 150 μE·m2·s−1 under a 16/8 h light/dark cycle. The nanoparticles synthesis methods influence the particle size, morphology, density, surface area to generate growth inhibition and further algal deaths at the nanoparticle-dependent concentration. Moreover, the results revealed that nanoparticles caused a more potent inhibitory effect on microalgal growth and severely disrupted algal cells’ membranes.

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Economic and environmental assessment of bacterial poly(3-hydroxybutyrate) production from the organic fraction of municipal solid waste

Bioresources and Bioprocessing ◽

10.1186/s40643-021-00392-4 ◽

2021 ◽

Vol 8 (1) ◽

Author(s):

Jon Kepa Izaguirre ◽

Leire Barañano ◽

Sonia Castañón ◽

José A. L. Santos ◽

M. Teresa Cesário ◽

...

Keyword(s):

Municipal Solid Waste ◽

Solid Waste ◽

Environmental Assessment ◽

Basal Medium ◽

Economic Feasibility ◽

Limiting Factors ◽

Organic Fraction ◽

Extraction Solvent ◽

Experimental Parameters ◽

The Cost

AbstractThe management of municipal solid waste is a major logistic and environmental problem worldwide. Nonetheless, the organic fraction of municipal solid waste (OFMSW) is a valuable source of nutrients which can be used for a variety of purposes, according to the Circular Economy paradigm. Among the possible applications, the bioproduction of a biodegradable polyester, poly(3-hydroxybutyrate) [P(3HB)], using OFMSW as carbon platform is a promising strategy. Here, an economic and environmental assessment of bacterial P(3HB) production from OFMSW is presented based on previously published results. The SuperPro Designer® software was used to simulate P(3HB) production under our experimental parameters. Two scenarios were proposed depending on the fermentation medium: (1) enzymatic hydrolysate of OFMSW supplemented with glucose and plum waste juice; and (2) basal medium supplemented with glucose and plum waste juice. According to our results, both scenarios are not economically feasible under our experimental parameters. In Scenario 1, the low fermentation yield, the cost of the enzymes, the labour cost and the energy consumption are the factors that most contribute to that result. In Scenario 2, the cost of the extraction solvent and the low fermentation yield are the most limiting factors. The possibility of using process waste as raw material for the generation of other products must be investigated to enhance economic feasibility. From an environmental viewpoint, the photochemical oxidation potential (derived from the use of anisole as extraction solvent) and the generation of acid rain and global warming effect (caused by the burning of fuels for power generation) are the most relevant impacts associated to P(3HB) production under our experimental parameters.

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Antioxidant potential and optimization of production of extracellular polysaccharide by Acinetobacter indicus M6

Journal of Genetic Engineering and Biotechnology ◽

10.1186/s43141-021-00137-y ◽

2021 ◽

Vol 19 (1) ◽

Author(s):

Ch. Ravi Teja ◽

Abraham P. Karlapudi ◽

Neeraja Vallur ◽

K. Mamatha ◽

D. John Babu ◽

...

Keyword(s):

Antioxidant Activities ◽

Radical Scavenging Activity ◽

Radical Scavenging ◽

Basal Medium ◽

Extracellular Polysaccharide ◽

Extracellular Polysaccharides ◽

Scavenging Activity ◽

Promising Alternative ◽

Food Engineering ◽

The Face

Abstract Background Extracellular polysaccharides (ECPs) produced by biofilm-producing marine bacterium have great applications in biotechnology, pharmaceutical, food engineering, bioremediation, and bio-hydrometallurgy industries. The ECP-producing strain was identified as Acinetobacter indicus M6 species by 16S rDNA analysis. The polymer produced by the isolate was quantified and purified and chemically analyzed, and antioxidant activities have been studied. The face-centered central composite design (FCCCD) was used to design the model. Results The results have clearly shown that the ECP was found to be endowed with significant antioxidative activities. The ECP showed 59% of hydroxyl radical scavenging activity at a concentration of 500 μg/mL, superoxide radical scavenging activity (72.4%) at a concentration of 300 μg/mL, and DPPH˙ radical scavenging activity (72.2%) at a concentration of 500 μg/mL, respectively. Further, HPLC and GC-MS results showed that the isolated ECP was a heteropolymer composed of glucose as a major monomer, and mannose and glucosamine were minor monomers. Furthermore, the production of ECP by Acinetobacter indicus M6 was increased through optimization of nutritional variables, namely, glucose, yeast extract, and MgSO4 by “Response Surface Methodology”. Moreover the production of ECP reached to 2.21 g/L after the optimization of nutritional variables. The designed model is statistically significant and is indicated by the R2 value of 0.99. The optimized medium improved the production of ECP and is two folds higher in comparison with the basal medium. Conclusions Acinetobacter indicus M6 bacterium produces a novel and unique extracellular heteropolysaccharide with highly efficient antioxidant activity. GC-MS analyses elucidated the presence of quite uncommon (1→4)-linked glucose, (1→4)-linked mannose, and (→4)-GlcN-(1→) glycosidic linkages in the backbone. The optimized medium improved the production of ECP and is two folds higher in comparison with the basal medium. The newly optimized medium could be used as a promising alternative for the overproduction of ECP.

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Methylation of Arsenic by Freshwater Green Algae

Canadian Journal of Fisheries and Aquatic Sciences ◽

10.1139/f83-142 ◽

1983 ◽

Vol 40 (8) ◽

pp. 1254-1257 ◽

Cited By ~ 28

Author(s):

M. D. Baker ◽

P. T. S. Wong ◽

Y. K. Chau ◽

C. I. Mayfield ◽

W. E. Inniss

Keyword(s):

Green Algae ◽

Lake Water ◽

Sodium Arsenite ◽

Basal Medium ◽

Arsenic Species ◽

Freshwater Ecosystems ◽

Dimethylarsinic Acid ◽

Additional Source ◽

Arsenic Compounds ◽

Methylarsonic Acid

Isolates from four genera of freshwater green algae were capable of methylating sodium arsenite in lake water and Bold's basal medium. Analysis of the liquid phase of the methylation flasks revealed the presence of methylarsonic acid, dimethylarsinic acid, and trimethylarsine oxide. Volatile arsine and methylarsines were not detected in the headspace gases presumably because of the inability of the algae to reduce completely the methylated–arsenic species. Although the algae varied with respect to their methylating abilities, the levels of methylated–arsenic compounds were always significantly higher when the algae were grown in lake water. This may have been due to the lower phosphate concentration in the lake water. We suggest that arsenic methylation by green algae constitutes an additional source for the formation and cycling of organo-arsenic compounds in freshwater ecosystems.

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A medium, solidified with gellan gum, for determining the Na+ requirement of Vibrio species

Canadian Journal of Microbiology ◽

10.1139/m93-118 ◽

1993 ◽

Vol 39 (8) ◽

pp. 804-808 ◽

Cited By ~ 4

Author(s):

Lisa D. Noble ◽

John A. Gow

Keyword(s):

Marine Bacteria ◽

Solid Medium ◽

Specific Growth ◽

Basal Medium ◽

Gellan Gum ◽

Growth Responses ◽

Prolonged Incubation ◽

Low Sodium ◽

Growth Requirements ◽

Lag Period

Until now there has not been a satisfactory solid medium for determining the growth responses, to Na+, of marine and other bacteria that have specific growth requirements for Na+. A solid medium would be useful to investigators who would like to take advantage of the efficiency of multipoint inoculation when testing for a Na+ requirement. By using 1% gellan gum (Gel-GroTM) as the solidifying agent a medium was formulated that had a contaminating level of Na+ of slightly less than 2 mM in the basal medium. Two species of Aeromonas, which do not require Na+ for growth, and 31 species of Vibrio, which require Na+, were tested for their growth responses to Na+ on this medium. The Aeromonas strains grew well, within 24 h, at all of the Na+ concentrations tested. Approximately 75% of the Vibrio strains did not grow on the basal medium even after a prolonged incubation period. The remaining species were able to grow on the basal medium, but not without a lag period. These lag periods were as short as 36 h for two of the species and in some instances as long as 312 h. These lag periods were of sufficient duration to determine that Na+ stimulated the growth of the Vibrio strains that were able to grow on the basal medium. Approximately 75% of the strains, representing most species of Vibrio, were able to grow if as little as 25 mM Na+ was present in the medium.Key words: low-sodium medium, Na+ requirement, gellan gum, agar substitute, marine bacteria.

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Continuous in vitro culture of Babesia divergens in a serum-free medium

Parasitology ◽

10.1017/s0031182097008937 ◽

1997 ◽

Vol 115 (1) ◽

pp. 81-89 ◽

Cited By ~ 17

Author(s):

N. GRANDE ◽

E. PRECIGOUT ◽

M. L. ANCELIN ◽

K. MOUBRI ◽

B. CARCY ◽

...

Keyword(s):

Human Serum ◽

Reduced Glutathione ◽

Lipid Fraction ◽

Basal Medium ◽

Defined Medium ◽

Specific Lipids ◽

Serum Free ◽

Babesia Divergens ◽

Lipid Fractions

Babesia divergens was cultivated in RPMI 1640 (25 mM HEPES) supplemented with 10% human serum (RPMI-10% HS) with a high percentage of parasitized erythrocytes (PPE) ([ges ]40%). Standardization of in vitro tests, purification of exoantigens, biochemical studies and the safety of the culture handler motivated the development of a serum-free defined medium. Removal of serum greatly reduced the PPE but, after a period of adaptation, the culture was continuous and the parasite was able to develop a 3% routine PPE. Addition of vitamins or reduced glutathione in basal medium (RPMI) did not improve the PPE. The supplementation of basal medium with lipidic carrier (Albumax I or bovine serum albumin–Cohn's fraction V) promoted the growth of B. divergens with high PPE (>30%) close to those obtained in RPMI–10% HS. Neither protein nor lipid fractions alone were able to restore the growth of B. divergens. Nevertheless, the whole lipid fraction from serum or Albumax I added to delipidated albumin partially restored the growth (7% PPE), indicating that the presentation of specific lipids by a carrier is crucial for the parasite. All the data indicate that Albumax I can replace human serum offering the advantages of safety, standardization for chemosensitivity tests, and exoantigen purification.

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