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Method for extracting chitin from litopenaeus vannamei shells

A technology for chitin and prawns, applied in the biological field, can solve the problems of low efficiency, low decalcification rate and deproteinization rate, etc., and achieve the effect of high yield and high purity

Active Publication Date: 2020-03-06
INST OF OCEANOLOGY - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In recent years, the method of extracting chitin from shrimp and crab shells by fermentation has attracted widespread attention, but the low efficiency and low decalcification rate and deproteinization rate are still the difficulties that need to be solved urgently.

Method used

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  • Method for extracting chitin from litopenaeus vannamei shells
  • Method for extracting chitin from litopenaeus vannamei shells
  • Method for extracting chitin from litopenaeus vannamei shells

Examples

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Embodiment 1

[0021] 1) Preparation of Litopenaeus vannamei shell powder: firstly, the shells of Litopenaeus vannamei were cleaned with distilled water, and then dried in an oven for two days. Then crush the dried shrimp shells to 0.5-1.0 mm with a pulverizer, and set aside;

[0022] 2) Preparation of the strain seed solution: activate Lactobacillus rhamnosus tangarus in a conventional manner, and inoculate it into MRS medium for 12 hours after activation; activate Bacillus amyloliquefaciens in a conventional manner, and inoculate it into LB culture after activation cultured in medium for 12 hours.

[0023] 3) Inoculate the seed liquid of Lactobacillus rhamnosus in the above step 2) into 5 g of the above step 1) shrimp shell powder and 5 g of glucose mixture with an inoculation amount of 4% by volume; adjust the system to pH6.5, and then Fermented and cultured at 37°C for 48 hours; then the fermentation broth was centrifuged at 4000rpm for 10 minutes to collect the precipitate. At this tim...

Embodiment 2

[0030] 1) Preparation of Litopenaeus vannamei shell powder: firstly, the shells of Litopenaeus vannamei were cleaned with distilled water, and then dried in an oven for two days. Then crush the dried shrimp shells to 0.5-1.0 mm with a pulverizer, and set aside;

[0031] 2) Preparation of the strain seed solution: activate Lactobacillus rhamnosus tangarus in a conventional manner, and inoculate it into MRS medium for 12 hours after activation; activate Bacillus amyloliquefaciens in a conventional manner, and inoculate it into LB culture after activation cultured in medium for 12 hours.

[0032] 3) Inoculate the Lactobacillus rhamnosus seed solution in the above step 2) into 5 g of the above step 1) shrimp shell powder and 5 g of glucose mixture with an inoculation amount of 2% by volume; adjust the system to pH6.5, and then Ferment and cultivate at 37°C for 48 hours; then centrifuge the fermentation broth at 4000rpm for 10 minutes to collect the precipitate. At this time, the ...

Embodiment 3

[0035] 1) Preparation of Litopenaeus vannamei shell powder: firstly, the shells of Litopenaeus vannamei were cleaned with distilled water, and then dried in an oven for two days. Then crush the dried shrimp shells to 0.5-1.0 mm with a pulverizer, and set aside;

[0036] 2) Preparation of the strain seed solution: activate Lactobacillus rhamnosus tangarus in a conventional manner, and inoculate it into MRS medium for 12 hours after activation; activate Bacillus amyloliquefaciens in a conventional manner, and inoculate it into LB culture after activation cultured in medium for 12 hours.

[0037] 3) Inoculate the Lactobacillus rhamnosus seed liquid in the above step 2) into 1000g of the above step 1) shrimp shell powder and 1000g glucose mixture with an inoculation amount of 4% by volume; adjust the system to pH 6.5, and then 37°C, ferment and cultivate for 48 hours; then centrifuge the fermented liquid at 4000rpm for 10 minutes to collect the precipitate. At this time, the remo...

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Abstract

The invention relates to a biotechnology, and in particular, relates to a method for extracting chitin from litopenaeus vannamei shells. The method comprises the steps: fermenting in the shrimp shellsthrough lactobacillus rhamnosus, inoculating bacillus amyloliquefaciens, and fermenting to remove proteins in shrimp shell powder, and thus obtaining the chitin represented by a general formula I. The lactobacillus rhamnosus is used for removing calcium carbonate, then the proteins are removed by bacillus amyloliquefaciens, the chitin is extracted from the litopenaeus vannamei shell powder, and the method has the advantages that the yield is high, the purity of the obtained chitin is high, and no chemical reagent needs to be used.

Description

technical field [0001] The invention relates to biotechnology, in particular to a method for extracting chitin from the shell of Litopenaeus vannamei. Background technique [0002] Crustaceous waste management is a huge problem. Due to the lack of scientific waste treatment methods, a large amount of waste is directly discharged as processing wastewater without treatment. The shells of crustaceans are the most important source of commercial chitin. In recent years, the potential uses of chitin and chitosan in the agricultural, food, chemical, medical, pharmaceutical, cosmetic, and biomedical industries have been widely recognized. At present, the method of extracting chitin from the shell of discarded crustaceans is mainly chemical method. For many years, chemical methods have been used for large-scale preparation of chitin because of their simplicity, high efficiency and low cost. In the chemical method, it is mainly to use a large amount of strong acid and strong alkali...

Claims

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Application Information

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IPC IPC(8): C08B37/08
CPCC08B37/0003C08B37/003
Inventor 邢荣娥刘勇亮杨皓月李克成秦玉坤刘松于华华李鹏程
Owner INST OF OCEANOLOGY - CHINESE ACAD OF SCI