Production of Ethanol by Zymomonas Mobilis Mutant : The Effects of Sodium Acetate at pH 5 and No Control pH

Silicon (Si) is distributed throughout plant tissues, but its role in forages has not been clarified. Although Si has been suggested as an antiquality factor which limits the digestibility of structural carbohydrates, other research indicates that its presence in plants does not affect digestibility. We employed x-ray microanalysis to evaluate Si as an antiquality factor at specific sites of two cultivars of bermuda grass (Cynodon dactvlon (L.) Pers.). “Coastal” and “Tifton-78” were chosen for this study because previous work in our lab has shown that, although these two grasses are similar ultrastructurally, they differ in in vitro dry matter digestibility and in percent composition of Si.Two millimeter leaf sections of Tifton-7 8 (Tift-7 8) and Coastal (CBG) were incubated for 72 hr in 2.5% (w/v) cellulase in 0.05 M sodium acetate buffer, pH 5.0. For controls, sections were incubated in the sodium acetate buffer or were not treated.

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In Vitro Incorporation of Sodium Acetate-l-C14 into Leukocyte Lipids of Normal and Leukaemic Subjects as a Function of Incubation Time

Nuklearmedizin ◽

10.1055/s-0037-1621180 ◽

1962 ◽

Vol 02 (02) ◽

pp. 165-172

Author(s):

C Miras ◽

G Lewis ◽

J Mantzos

Keyword(s):

Sodium Acetate ◽

Linear Part ◽

Lipid Synthesis ◽

Normal Subjects ◽

Cytostatic Agents ◽

Time Intervals ◽

Total Blood ◽

Effect Of Treatment ◽

Product Relation

Summary1. Separated leukocytes or total blood from normal subjects, untreated leukaemic patients and from leukaemic patients treated with cytostatic agents were incubated with CH3COONa-l-C14. Radioactivity of mixed lipids was measured at standard time intervals.2. The time incorporation curve observed with leukocytes from treated leukaemic patients showed after an initial linear part, a more rapid levelling off than the curves observed with leukocytes from untreated and normal subjects.3. Therefore, an indirect effect of treatment on leukocyte lipid synthesis seems to be present.4. Phospholipid and neutral lipid synthesis by leukaemic leukocytes was also studied. The results give no evidence that these fractions as a whole have any precursor-product relation.

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Applicability of electrodialysis to the separation of sodium acetate from synthetic alkaline hardwood extract

TAPPI Journal ◽

10.32964/tj14.11.695 ◽

2015 ◽

Vol 14 (11) ◽

pp. 695-708 ◽

Cited By ~ 3

Author(s):

RAVIKANT PATIL ◽

CHI TRUONG ◽

JOSEPH GENCO ◽

HEMANT PENDSE ◽

ADRIAAN VAN HEININGEN

Keyword(s):

Current Density ◽

Sodium Sulfate ◽

Sodium Acetate ◽

Separation Efficiency ◽

Feed Concentration ◽

Initial Concentration ◽

White Liquor ◽

Complete Extraction ◽

Electro Osmosis ◽

Preliminary Separation

Our objective was to develop a process for recovering acetyl groups from industrial northeast hardwood chips. Extraction experiments showed that the white liquor charge of 6% effective alkali at 50°C and liquor-to-wood ratio of 4:1 leads to the complete extraction of acetyl groups from industrial hardwood chips. Electrodialysis was assessed as a technique for separating and concentrating sodium acetate from synthetic hardwood extract. Preliminary separation experiments using dilute sodium acetate showed that the sodium acetate can be concentrated up to approximately 24% by weight from an initial concentration of about 2% by weight. The effects of current density, feed concentration, electro-osmosis, and osmosis on the separation of sodium acetate were evaluated. Finally, selectivity experiments were performed to study the effect of various components of the white liquor on the separation of sodium acetate. Fully oxidized synthetic white liquor was used in selectivity experiments to avoid deleterious effects of Na2S. Selectivity experiments using synthetic oxidized white liquor showed a significant decrease in the separation efficiency due to the presence of sodium hydroxide, sodium carbonate, and sodium sulfate in the synthetic extract.

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Nomenclature Abstract for Zymomonas mobilis francensis Coton et al. 2006.

The NamesforLife Abstracts ◽

10.1601/nm.11159 ◽

2003 ◽

Author(s):

Charles Thomas Parker ◽

George M Garrity

Keyword(s):

Zymomonas Mobilis

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Synthesis and Caracterization of some New 1H-3-aryl-7-etoxycarbonyl-6-methyl-pyrazolo[5,1-c][1,2,4]triazoles

Revista de Chimie ◽

10.37358/rc.08.1.1703 ◽

2008 ◽

Vol 59 (1) ◽

pp. 41-44

Author(s):

Maria-Daniela Sofei ◽

Maria Ilici ◽

Valentin Badea ◽

Carol Csunderlik ◽

Vasile-Nicolae Bercean

Keyword(s):

Mass Spectrometry ◽

Acetic Acid ◽

Nmr Spectroscopy ◽

Sodium Acetate ◽

Glacial Acetic Acid ◽

Ir And Nmr Spectroscopy

The synthesis of 1H-3-aryl-7-ethoxycarbonyl-6-methyl-pyrazolo[5,1-c][1,2,4]triazoles (2) was carried out by cyclization of 1H-5-arylidenehydrazino-4-ethoxycarbonyl-3-methyl-pyrazoles (1) in the presence of bromine using glacial acetic acid as solvent and sodium acetate as base. The new nine obtained compounds were characterized by IR and NMR spectroscopy and mass spectrometry.

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Novel Synthesis of 4-Benzylidene-2-((1-phenyl-3,4-dihydroisoquinoline-2(1H)-yl)methyl) oxazol-5(4H)-one Derivatives Using 1,2,3,Tetrahydroisoquinoline and their Antimicrobial Activity

Current Organic Synthesis ◽

10.2174/1570179417666200415151228 ◽

2020 ◽

Vol 17 (5) ◽

pp. 396-403

Author(s):

Nalla Krishna Rao ◽

Tentu Nageswara Rao ◽

Botsa Parvatamma ◽

Y. Prashanthi ◽

Ravi Kumar Cheedarala

Keyword(s):

Antimicrobial Activity ◽

Antibacterial Activity ◽

Acetic Acid ◽

Sodium Acetate ◽

Good Activity ◽

Activity Profile ◽

Aryl Aldehydes ◽

Chemical Structures ◽

Novel Synthesis ◽

Target Molecules

Aims: A series of six 4-benzylidene-2-((1-phenyl-3,4-dihydro isoquinoline-2(1H)-yl)methyloxazol- 5(4H)-one derivatives were synthesized by condensation of substituted aryl aldehydes with 2-(2-(1-phenyl-3,4- dihydro isoquinoline-2(1H)-acetamido)acetic acid in the presence of sodium acetate, acetic anhydride and zinc oxide as catalysts. Background: Novel Synthesis of 4-Benzylidene-2-((1-phenyl-3,4-dihy droisoquinoline-2(1H)-yl)methyl)oxazol- 5(4H)-one derivatives using 1,2,3,Tetrahydroisoquinoline and their antimicrobial activity. Objective: The title compounds can be synthesized from 1,2,3,4-tetrahydroisoquinoline. Methods: The target molecules, i.e., 4-benzylidene-2-((1-phenyl-3, 4-dihydro isoquinoline-2(1H)-yl) methyl) oxazol-5(4H)-one derivatives (8a-8f) have been synthesized from 1,2,3,4-tetrahydroisoquinoline which was prepared from benzoic acid in few steps. Results: All the six compounds were evaluated based on advanced spectral data (1H NMR, 13C NMR & LCMS), and the chemical structures of all compounds were determined by elemental analysis. Conclusion: Antibacterial activity of the derivatives was examined for the synthesized compounds and results indicate that compound with bromine substitution has a good activity profile.

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