79 results about "D-arabitol" patented technology

A fungal microorganism can be engineered by means of genetic engineering to utilise L-arabinose. The genes of the L-arabinose pathway, which were unknown, i.e. L-arabinitol 4-dehydrogenase and L-xylulose reductase, were identified. These genes, together with the known genes of the L-arabinose pathway, form a functional pathway. This pathway can be introduced to a fungus, which is completely or partially lacking this pathway.

The invention relates to a novel admixture for mineral binders, composed of a composition containing at the same time a sugar or an oxidized sugar and a hydrogenated sugar. The oxidized sugar may consist, in particular, of gluconic acid or one of its salts or an oxidized starch hydrolysate. The hydrogenated sugar may consist in particular of maltitol, sorbitol, mannitol, xylitol, arabitol, or a hydrogenated starch hydrolysate containing at least 40% by weight of maltitol. Within the admixture, this composition may be combined with conventional admixtures such as phosphates, borates, or amines. The combination of a sugar or an oxidized sugar and a hydrogenated sugar within this composition makes it possible to obtain synergistic effects, particularly in terms of plasticity and mechanical properties of the mineral binders. The admixtures claimed may be used equally well for admixing with cements, raw materials for cements as for admixing with mortars, slurries and concretes. They may also be used in other sectors such as, for example, the plaster industry, particularly as complexing agents or hydration or dehydration controllers.

The invention discloses a technique for producing xylitol and dulcitol simultaneously, comprising the following steps: (1) diluting xylose mother liquor, carrying out chromatographic separation after decoloration, filtering and ion exchange and obtaining mixed liquor; (2) preparing the xylitol: adding nutritional components into the mixed liquor, inoculating yeast seed liquor after sterilization, carrying out fermentation and obtaining fermentation liquor; (3) filtering the fermentation liquor to remove the yeast, then carrying out decoloration, filtering and ion exchange, and then obtaining crystalline xylitol by evaporation, concentration and crystallization; (4) carrying out evaporation and concentration on the mixed liquor of galactose and arabitol obtained by chromatographic separation in the step (1), concentrating to the mass concentration of 35 to 45 percent, and then carrying out catalytic hydrogenation, thus obtaining the mixed liquor of the dulcitol and the arabitol; and (5) carrying out decoloration, filtering and ion exchange on the obtained mixed liquor, putting the mixed liquor into a crystallization kettle for evaporation till supersaturation, adding dulcitol seed crystal and seed crystal growth promoter, and carrying out crystallization to obtain crystalline dulcitol.

The invention discloses a Gluconobacter oxydans, which is classified and named as Gluconobacter oxydans NH-10, and preserved in China General Microbiological Culture Center of Microbial Culture Collection Management Committee with the preservation number of CGMCC No.2709. The invention further discloses a D-xylulose preparation method that uses the Gluconobacter oxydans. The strain obtained by screening can transform D-Arabitol so as to generate D-xylulose in high efficiency, the D-xylulose preparation method reaches the highest D-Arabitol transformation ratio of 99.5 percent (w/w) and the D-xylulose yield ratio of 95 percent, the D-xylulose concentration of a conversion fluid can reach 95g/L, and the conversion fluid hardly contains other ingredients.

A novel article and method are disclosed for reducing malodor in disposable products for the absorption of body fluids. An effective amount of pentitol is applied to a disposable absorbent material, prior to its use. In one aspect, the invention provides a water-swellable, water-insoluble, hydrogel-forming polymeric absorbent material. In one aspect, the pentitol is compositionally part of the absorbent structure or is coated on the absorbent material present in the absorbent structure. The pentitol preferably is located in the area of insult, i.e., that area of the absorbent product to be exposed to the body fluid intended to be absorbed. The pentitol in the novel article and method of the present invention is a compound selected from the group consisting of ribitol, D-arabinitol, L-arabinitol, and xylitol or a combination of one or more compounds selected from the group consisting of ribitol, D-arabinitol, L-arabinitol, and xylitol effective in preventing malodor.

The invention relates to an activated carbon-loaded type ruthenium catalyst and a preparation method and application thereof in preparation of sugar alcohols by catalytic hydrogenation of saccharides.The preparation method comprises the following steps of loading metal ruthenium onto the activated carbon by a simple impregnating reduction method, so as to prepare the loaded type Ru/C (ruthenium/carbon) catalyst with high dispersion degree; further applying the Ru/C catalyst into the hydrogenation process of a series of saccharides, such as xylose, arabinose, glucose, mannose and maltose, so as to prepare xylitol, arabitol, sorbitol, mannitol and maltitol at high efficiency. The activated carbon-loaded type ruthenium catalyst has the advantages that under certain reaction conditions, the high conversion rate of series saccharides and the high selectivity of sugar alcohols can be realized, the stability of the catalyst is good, the recycling is convenient, and the frequency of cyclic use is high; the preparation technology is simple, the production cost is low, the catalytic activity is high, and the preparation technology is suitable for preparing multiple types of sugar alcohols,has good universality and is suitable for being popularized.

The invention discloses a method for producing xylitol through using xylose mother liquor or xylitol mother liquor depleted during the production of xylitol. The method comprises the following: 1 a step of adding hydrogen into arabinose separated from the xylose mother liquor to obtain D-arabitol or separating after adding hydrogen to obtain the D-arabitol; 2 a step of converting the D-arabitol obtained during the step 1 or the D-arabitol in the xylitol mother liquor into xylitol through making use of a strain simultaneously containing D-arabitol dehydrogenase and xylitol dehydrogenase; 3 a step of concentrating and crystallizing the xylitol conversion liquor obtained during the step 2 to obtain an xylitol product after removing thallus cells. The method which makes full use of the xylose mother liquor and xylitol mother liquor produced by a traditional method with simple and reasonable process can improve the utilization factor of raw materials such as corn cob and bagasse by about 9 to 14 percent, thereby greatly reducing the total production cost and consequently improving the economic efficiency of xylitol production.

The invention relates to a method for preparing xylitol by a complex enzyme method, the obtained xylitol and the application of the xylitol. The method is as follows: arabitol oxidizing dehydrogenase, xylitol reductase and inductive agent xylitol are added into d-arabitol, calcium carbonate and sugar so as to prepare the xylitol. The method has strong continuous operability, low equipment investment and operation cost, easy operation and industrialization realization and very high conversion rate and production rate of the xylitol. The xylitol prepared by the method can be used for tobacco products.

The invention provides a method for producing D-arabitol from Hansenula polymorpha mutant strain and Hansenula polymorpha. A gene engineering technique is mainly utilized to obtain a D-arabitol high-yield mutant strain by establishing a Hansenula polymorpha acid phosphatase gene mutant strain. The method has the advantages of low cost and short production cycle, is easy to operate, and provides a new way for solving the problem of shortage of D-arabitol sources. The mutant strain is supplemented by batches through glucose to perform biotransformation so as to produce the D-arabitol; and the conversion rate of the substrate glucose is 51.2%, which is obviously higher than the conversion rate of the substrate glucose when the initial strain is supplemented by batches through glucose to perform biotransformation so as to produce the D-arabitol.

The invention relates to a method for catalyzing sugar and sugar alcohol hydrocracking reaction through a nickel-based catalyst. Under the action of the nickel-based catalyst, the aqueous solution of xylose, glucose, fructose, arabinose, xylitol, sorbitol, arabitol and other carbon-rich sugar and sugar alcohol is adopted as the raw material, the raw material is subjected to the hydrogenation dehydration and decomposed into low-carbon alcohols in a highly selective manner, and the low-carbon alcohols mainly comprise ethanediol, 1,2-propylene glycol and 1,3-propylene glycol.

The invention discloses a method for simultaneous rapid detection of various sugars, sugar alcohols and alcohols in beer, belonging to the technical field of analytical chemistry. In the method provided by the invention, an integrated pulsed amperometric-ion chromatography is used, by optimization of a pretreatment detection method, experimental factors influencing separation of constituents are researched, and a method for simultaneously detecting 23 types of sugars, sugar alcohols and alcohols (2, 3-butanediol, ethyl alcohol, methanol, glycerin, erythritol, xylitol, fucose, arabitol, sorbitol, trehalose, ribovitol, mannitol, 2-DNA-D-glucose, mannose, melibiose, glucose, maltitol, fructose, lactose, ribose, sucrose, raffinose and maltitol ) in the beer is built one time. Thus, a technicalproblem of accurate analysis on multiple constituents including the sugars, the sugar alcohols and the alcohols in the beer is solved, the method provided by the invention is rapid, accurate and sensitive, realizes simultaneous analysis of multiple types and multiple constituents, and makes an important contribution to detection of beer constituents.

The invention discloses a preparation method of gluconobacter oxydans engineering bacteria, which performs over-expression of the key restriction enzyme glucose-6-phosphate dehydrogenase (G6PDH) for controlling the phosphopentose path to increase the metabolic flux of the path so as to realize cyclic regeneration of coenzyme NADH. The invention also discloses a fermentation technology of the engineering bacteria and application thereof in converting and preparing xylitol. According to the invention, the effect of the engineering bacteria in converting D-arabitol to generate xylitol is obviously superior to that of an original strain; and the conversion rate of xylitol against D-arabitol can reach 60-90%. The technology solves the problems of low conversion rate and low xylitol concentration of a bioconversion method for preparing xylitol to a certain degree, and has the advantages of economy and practicability, simplicity and convenience in operation and energy conservation and environmental protection.

The invention discloses a method for simultaneously detecting 22 sugars, sugar alcohol and alcohol in fruit juice, and belongs to the field of analytical chemistry. The method adopts an integral impulse ampere-ion chromatography to research experiment factors affecting component separation via a processing method before optimization; and the method for simultaneously detecting the 22 sugars, the sugar alcohol and the alcohol (2,3-butanediol, propylene glycol, methyl alcohol, glycerin, erythritol, xylitol, rhamnose, arabitol, sorbitol, trehalose, galactitol, mannitol, 2-deoxidized-D-glucose, arabinose, melibiose, glucose, galactose, fructose, ribose, saccharose, raffinose and maltose) at a time is built. The technical difficulty of accurately analyzing the plurality of components, sugars, sugar alcohol and alcohol, in the fruit juice is solved; the method is fast, accurate and sensitive, achieves simultaneous analysis of the plurality of categories and the plurality of components, and makes an important contribution to component detection of the fruit juice.

The invention discloses a hyphopichia burtonii strain and applications of the hyphopichia burtonii strain. The hyphopichia burtonii strain has the following morphological characteristics: the strain is inoculated to a PDA culture medium through a streak inoculation method, culturing is carried out for 2d at 28 DEG C, the diameter of the bacterial colony is 5-8 mm, the bacterial colony is round-jellyfish-shaped, is milk white in color, has the butyrous texture, and is non-transparent, and the edge of the bacterial colony is blanket-shaped. The hyphopichia burtonii strain can be used for producing arabitol in Maotai-flavor baijiu.

The invention provides a screening method of a D-arabitol high-yield yeast mutant strain. By using a mutant strain obtained by carrying out mutagenesis on Kluyveromyces lactis by a low-energy N+ ion implantation technique as a screening object, a high-flux screening method, which is implemented by primary screening based on a high-sugar solid culture medium and secondary screening based on paper chromatography/high-performance liquid chromatography combination, is established. The method has the advantages of high screening efficiency, low cost, short screening period and the like, is easy to operate, and provides a new method for efficiently screening the D-arabitol high-yield strain by modifying the yeast with low-energy ion implantation.

The invention relates to a method for preparing arabitol by flammulina velutipes, which utilizes the characteristic that flammulina velutipes sporocarp contains rich arabitol to prepare the low-cost and environment-friendly arabitol by taking the flammulina velutipes sporocarp as a raw material; and the product can be taken as natural sweetener and functional food raw material. The method comprises the steps of: drying the fresh flammulina velutipes sporocarp, and then using high-concentration alcohol to soak or carry out reflux extraction on the dried flammulina velutipes sporocarp; carrying out vacuum concentration on the leach liquor to recover ethanol; putting the concentrated solution in the environment of 0-10 DEG C; separating out the arabitol by crystallization; filtering or centrifuging while the arabitol is cool to obtain arabitol crystal; then, carrying out recrystallization on the arabitol crystal by methanol; continuously carrying out vacuum concentration on the separated mother liquor of the crystal to recover ethanol; and repeating the operation of crystallization and recrystallization to improve the yield of the arabitol. In order to save the cost, the method is more suitable for taking defective flammulina velutipes sporocarp or the head cut from the flammulina velutipes sporocarp as raw material. The technology has the characteristics of being simple in equipment, saving the cost and protecting the environment, thus improving the economic benefit of the flammulina velutipes industry.

Novel compounds, called liamocins from Aureobasidium pullulans, having the general structure in Formula 1 are disclosed.

where R₁ is either COCH₃ or H; and R₂ is between two to ten O-linked 3,5-dihydroxydecanoate; and R₃ can be a polyol (e.g., L- or D-glycerol, L- or D-threitol, L- or D-erythritol, L- or D-arabitol, L- or D-xylitol, L- or D-lyxitol, L- or D-ribitol, L- or D-allitol, L- or D-altritol, L- or D-mannitol, L- or D-iditol, L- or D-gulitol, L- or D-glucitol (also called sorbitol), L- or D-galactitol (also called dulcitol), and L- or D-talitol), 2-amino-D-mannitol, 2N-acetylamino-D-mannitol, L-rhamnitol, or D-fucitol; except when R₃ is D-mannitol, R₂ is not 2 nor 3 O-linked 3,5-dihydroxydecanoate chains. These liamocins described above in addition to D-mannitol liamocin A1, D-mannitol liamocin A2, D-mannitol liamocin B1, and D-mannitol liamocin B2, alone or in combination with each other, can be used to kill certain bacteria and to treat certain bacterial infections.

The invention discloses a method for preparing D-xylosone by microbial transformation of glucose, comprising the following steps: firstly, respectively preparing an osmophilic yeast seed liquid and a gluconobacter oxydans seed liquid by using glucose as a raw material, then inoculating the osmophilic yeast seed liquid to conduct arabitol fermentation, and then in middle and later stage inoculating the gluconobacter oxydans seed liquid to conduct mixed culture fermentation, simultaneously controlling the glucose content in the broth to be 5-10g/L, and converting arabitol into D-xylosone. According to the method, the feedback inhibition of arabitol is removed, and the efficiency of preparing D-xylosone from glucose is raised. The invention further discloses a method for preparing xylitol by microbial transformation of glucose, comprising the following steps: firstly converting glucose into D-xylosone by the above method, then converting D-xylosone into D-xylose by isomerization of enzyme, extracting and refining, and conducting catalytic hydrogenation to obtain xylitol. According to the method, the production efficiency of xylitol is raised, and the cost of preparing xylitol by biological method is reduced.

The invention discloses a Candida bacterial strain and a method for producing D-arabitol. The Candida sp.H2 has the preservation number of CGMCC No.3255 in China Committee of Culture Collection for Microorganisms (CCCCM), and the 26S rDNA D1/D2 region sequence of the bacterial strain is displayed in SEQ IC NO:1. In the invention, the method using the Candida bacterial strain to produce D-arabitol is as follow: cultivating the Candida bacterial strain in a seed liquid culture medium containing glucose and yeast extracts to obtain the inoculum of Candida; then inoculating the inoculum of Candida to the seed liquid culture medium containing glucose and yeast extracts to ferment and produce D-arabitol. Compared with the prior art, the invention provides a new Candida bacterial strain which can be used for producing D-arabitol. The D-arabitol produced with the Candida sp.H2 of the invention has higher yield, and the accumulation amount can reach the high level of 86.55g.