Effects of Glucose Fermentation Products on Determination of Mannitol by Periodate-Titrametric Method.

1949 ◽  
Vol 70 (4) ◽  
pp. 677-678
Author(s):  
A. B. Kendrick ◽  
W. P. Swisher ◽  
R. A. Forrest
Minerals ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 344
Author(s):  
Svetlana Bortnikova ◽  
Natalya Abrosimova ◽  
Nataliya Yurkevich ◽  
Valentina Zvereva ◽  
Anna Devyatova ◽  
...  

This paper demonstrates the results of experiments for the determination of the composition of gases during the dehydration of sulfates (Na-jarosite, melanterite, and chalcanthite) collected at the surface of pyrometallurgical waste heaps. The volatilization of various elements, and vapor–gas phase transport from three sulfate groups were investigated by stepwise laboratory heating at 45, 55, and 65 °C. The sample of yellow efflorescence mainly consisted of Na-jarosite, the white efflorescence contained melanterite as the major mineral, and the blue efflorescence sample consisted of chalcanthite. These all contained a few impurities up to 5 %. The highest total dissolved solids (TDS) was found in the gas condensates from melanterite (59 mg/L), followed by chalcanthite (29 mg/L) and Na-jarosite (17 mg/L). It was determined that major and trace elements in the condensate can be trapped by water vapor and can migrate with the vapor phase during the desorption and dehydration of hydrous sulfates. X-ray diffractograms showed that Na-jarosite remained stable throughout the temperature range, whilst the separation of melanterite’s structural water occurred at 40 °C, and chalcanthite completely lost two water molecules at 50 °C. The gas condensates contained acetates and formates, which could be the fermentation products of bacterial communities. Some of the strains—Micrococcaceae sp., Bacillus sp., and Microbacteriaceae sp.—were cultivated.


2014 ◽  
Vol 16 (7) ◽  
pp. 3501-3507 ◽  
Author(s):  
Jayeon Baek ◽  
Tae Yong Kim ◽  
Wooyoung Kim ◽  
Hee Jong Lee ◽  
Jongheop Yi

An alternative biomass-based route to the petrochemical process for the production of 1,3-butadiene has been developed using glucose fermentation products.


2015 ◽  
Vol 98 (2) ◽  
pp. 397-409 ◽  
Author(s):  
Mary Beth Hall ◽  
J Arbaugh ◽  
K Binkerd ◽  
A Carlson ◽  
T Doan ◽  
...  

Abstract Starch, glycogen, maltooligosaccharides, and other α-1,4- and α-1,6-linked glucose carbohydrates, exclusive of resistant starch, are collectively termed "dietary starch". This nutritionally important fraction is increasingly measured for use in diet formulation for animals as it can have positive or negative effects on animal performance and health by affecting energy supply, glycemic index, and formation of fermentation products by gut microbes. AOAC Method 920.40 that was used for measuring dietary starch in animal feeds was invalidated due to discontinued production of a required enzyme. As a replacement, an enzymatic-colorimetric starch assay developed in 1997 that had advantages in ease of sample handling and accuracy compared to other methods was considered. The assay was further modified to improve utilization of laboratory resources and reduce time required for the assay. The assay is quasi-empirical: glucose is the analyte detected, but its releaseis determined by run conditions and specification ofenzymes. The modified assay was tested in an AOAC collaborative study to evaluate its accuracy and reliability for determination of dietary starch in animalfeedstuffs and pet foods. In the assay, samples are incubated in screw cap tubes with thermostable α-amylase in pH 5.0 sodium acetate buffer for 1 h at 100°C with periodic mixing to gelatinize and partially hydrolyze α-glucan. Amyloglucosidase is added, and the reaction mixture is incubatedat 50°C for 2 h and mixed once. After subsequent addition of water, mixing, clarification, and dilution as needed, free + enzymatically released glucose are measured. Values from a separate determination of free glucose are subtracted to give values forenzymatically released glucose. Dietary starch equals enzymatically released glucose multiplied by 162/180 (or 0.9) divided by the weight of the as receivedsample. Fifteen laboratories that represented feed company, regulatory, research, and commercial feed testing laboratories analyzed 10 homogenous test materials representing animal feedstuffs and pet foods induplicate using the dietary starch assay. The test samples ranged from 1 to 70% in dietary starch content and included moist canned dog food, alfalfa pellets, distillers grains, ground corn grain, poultry feed, low starch horse feed, dry dog kibbles, complete dairy cattle feed, soybean meal, and corn silage.Theaverage within-laboratory repeatability SD (sr) for percentage dietary starch in the test samples was 0.49 with a range of 0.03 to 1.56, and among-laboratory repeatability SDs (sR) averaged 0.96 with a range of 0.09 to 2.69. The HorRat averaged 2.0 for all test samples and 1.9 for test samples containing greater than 2% dietary starch. The HorRat results are comparable to those found for AOAC Method 996.11, which measures starch in cereal products. It is recommended that the dietary starch method be accepted for Official First Action status.


2021 ◽  
Vol 213 (10) ◽  
pp. 40-47
Author(s):  
G Kosovskiy ◽  
Elena Kolesnik ◽  
Dmitriy Popov

Abstract. The purpose of this work is to approve a device for studying the microbiome of the gastrointestinal tract of mammals. The study of the quantitative and qualitative composition of the digestive tract microbiota is one of the promising directions in metagenomics. Knowledge obtained about the organization of microbiocenosis genome, the determination of species composition and study of metabolic relationships between its representatives not only expand the understanding of its role in the process of evolution, speciation and breeding but also provide a scientifically substantiated basis for targeting changes in the microbiome to form a phenotype (optimization of feed bioconversion, increasing overall resistance, etc.). Scientific novelty. For the first time, the main characteristics of cellulolytic bacteria isolated from the chyme of the rabbit cecum were isolated, cultured and described through a chronic fistula. Methods. In order to carry out research aimed to study mammalian microbiome and its correction, the need arises to develop methods of obtaining microbiome samples from experimental animals. To obtain access to the chyme of the cecum in 7 rabbits for up to 3 months the chronic fistulas developed in Scientific Research Institute of Fur-Bearing Animal Breeding and Rabbit Breeding n. a. V. A. Afanas’ev were installed. No negative manifestations were observed in the animals after installation of the fistulas, no changes in appetite were detected, and complete healing of the skin wound was determined on the 9th day. Diagnostic laparotomies performed 3 months after fistula placement revealed no pathological processes in any of the studied animals. Results. Characteristics of cellulolytic bacteria of the rabbit cecum Butirivibrio fibrisolvens and Ruminococcus flavefaciens were studied. Data on their enzymatic effects on dietary components, fermentation products, digestion and formation of organic substances and chemical compounds are presented.


Molecules ◽  
2020 ◽  
Vol 25 (23) ◽  
pp. 5739
Author(s):  
Lin-Xiu Guo ◽  
Yue Tong ◽  
Jue Wang ◽  
Guo Yin ◽  
Hou-Shuang Huang ◽  
...  

Short-chain fatty acids (SCFAs) are the main microbial fermentation products from dietary fibers in the colon, and it has been speculated that they play a key role in keeping healthy in the whole-body. However, differences in SCFAs concentration in the serum and colon samples had attracted little attention. In this study, we have optimized the extract and analysis methods for the determination of ten SCFAs in both serum and colon content samples. Methanol and acetonitrile were chosen for extraction of SCFAs from serum and colon content samples, respectively. Biological samples were collected from Alzheimer’s disease rats treated by extract of Schisandra chinensis (Turcz.) Baill (SC-extract) were taken as research objects. The results showed that, the relative peak intensities of SCFAs in the colon content from all groups were quite similar, and the trend was identical in the serum samples. Compared with the values in humans, the ratio of ten SCFAs in rat’s colon was similar, while the percent of acetate in rat’s serum was significantly higher. For therapy of Alzheimer’s disease (AD), SC-extract decreased the concentration of butyrate, 3-Methyvalerate, and caproate in the serum samples towards the trend of normal rats. This study may help our understanding of how SCFAs are transported across colonic epithelium in healthy and diseased organisms.


Sign in / Sign up

Export Citation Format

Share Document