A kind of evaluation method of Aspergillus niger gluten spore activity

A technology of Aspergillus niger bran koji and evaluation method, which is applied in the directions of microorganism-based methods, biochemical equipment and methods, and microbial determination/inspection, etc. problems such as poor wall permeability, to achieve the effect of improving the utilization rate of raw materials, fast detection, and improving seed vigor

Active Publication Date: 2017-05-03
JIANGNAN UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these detection methods have disadvantages such as long operation process, reaction reagents need to be prepared immediately, MTT is carcinogenic, and the equipment is expensive.
[0005] Aspergillus bran spores are special dormant bodies of Aspergillus niger. The spore wall is thick and has poor permeability, making it difficult for foreign substances to intervene. At the same time, the force between spores is strong, and the spores adhere together, making it difficult to form uniformly dispersed single spores; Therefore, there are few reports about the research on the viability of Aspergillus niger gluten spores

Method used

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  • A kind of evaluation method of Aspergillus niger gluten spore activity
  • A kind of evaluation method of Aspergillus niger gluten spore activity

Examples

Experimental program
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Effect test

Embodiment 1

[0027] Configure PDA plate, test tube slant and eggplant bottle culture medium. The corn cob granules and water are evenly mixed according to the ratio of 1:1, the corn steep liquor is added to adjust the total nitrogen content (TN=1%-3%), and sterilized to obtain the bran bent barrel culture medium. Inoculate Aspergillus niger strains on PDA plate medium for activation, and incubate in an incubator at 35-38°C for 40-48 hours; pick a single colony and inoculate the slope of the test tube, incubator at 35-38°C, and cultivate for 5-7 days to obtain mature Aspergillus niger spores ;Pick a ring of test tube slant spores, inoculate eggplant bottle medium, culture at 35-38°C for 8-10 days to obtain mature Aspergillus niger spores; wash eggplant bottle spores with sterile water to obtain spore suspension, and transfer to bran yeast barrel, turning the barrel 2 to 3 times a day, and culturing at 35 to 38°C for 8 to 10 days to obtain mature spores of Aspergillus niger.

[0028] Take a...

Embodiment 2

[0032] Configure PDA plate, test tube slant and eggplant bottle culture medium. The corn cob granules and water are evenly mixed according to the ratio of 1:1, the corn steep liquor is added to adjust the total nitrogen content (TN=1%-3%), and sterilized to obtain the bran bent barrel culture medium. Inoculate Aspergillus niger strains on PDA plate medium for activation, and incubate in an incubator at 35-38°C for 40-48 hours; pick a single colony and inoculate the slope of the test tube, incubator at 35-38°C, and cultivate for 5-7 days to obtain mature Aspergillus niger spores ;Pick a ring of test tube slant spores, inoculate eggplant bottle medium, culture at 35-38°C for 8-10 days to obtain mature Aspergillus niger spores; wash eggplant bottle spores with sterile water to obtain spore suspension, and transfer to bran yeast barrel, turning the barrel 2 to 3 times a day, and culturing at 35 to 38°C for 8 to 10 days to obtain mature spores of Aspergillus niger.

[0033] Get a ...

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Abstract

The invention discloses a method for evaluating the activity of aspergillus niger mouldy bran spore. The method comprises the following steps: (1) washing cultured aspergillus niger mouldy bran spore with a phosphate buffer liquid, and filtering, thereby obtaining aspergillus niger mouldy bran spore suspension; (2) adding 0.055% (v / v) of Tween 80, and performing ultrasonic treatment, thereby obtaining uniformly dispersed monospore suspension, and adjusting the concentration of the monospore suspension to be 10<6>-10<7> pieces / mL; (3) preparing a 8-14mg / L methylene blue solution from the phosphate buffer liquid; (4) uniformly mixing the solutions of the steps (2) and (3) according to a ratio (v / v) of 1:1, sealing to react for 420 seconds, and scanning an absorbancy-time curve at the wavelength of 663nm; (5) testing the primary absorbancy and the absorbancy after the reaction is completed, of a reaction system, and representing the activity of cells according to the change of the absorbancy. By adopting the method, the culture time of mature seeds can be effectively shortened, the raw material utilization rate can be increased, and the technique is also applicable to evaluation on the activity of other microorganism spore.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a method for evaluating the activity of Aspergillus niger aspergillus gluten spores. Background technique [0002] Citric acid (Citric Acid) is an important organic acid with multiple functions, widely used in food, medicine, chemical industry and other fields; it is the edible organic acid with the largest output and consumption in the world, with a global output of more than 1.7 million tons. At the same time, citric acid has excellent biological characteristics, and has great application potential in emerging industries such as biopolymerization, drug delivery, and cell culture, and its demand is growing at a rate of 5% per year. [0003] Aspergillus niger is an important industrial microorganism. It is favored by the citric acid industry because of its safe enzyme system, various types of carbon sources, strong acid production ability, and strong acid resistance ability. In indu...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/02C12R1/685
Inventor 石贵阳陈坚王宝石张杰胡志杰蒋小东孙福新张梁李由然丁重阳李赢顾正华
Owner JIANGNAN UNIV
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