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Saccharomyces cerevisiae deleted bacterial strain and application thereof in furfural resistant aspect

A technology of Saccharomyces cerevisiae and strains, applied in the direction of fermentation, fungi, and microorganism-based methods, etc., can solve the problems of reducing ethanol production efficiency, achieve large scale, high efficiency, and improve tolerance

Inactive Publication Date: 2012-07-18
JIANGNAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, various fermentation inhibitors are produced during the production of ethanol from cellulose, which greatly reduces the production efficiency of ethanol

Method used

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  • Saccharomyces cerevisiae deleted bacterial strain and application thereof in furfural resistant aspect
  • Saccharomyces cerevisiae deleted bacterial strain and application thereof in furfural resistant aspect

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Example 1 Furfural resistance experiment of Saccharomyces cerevisiae deletion strain KKSC1

[0022] Take the Saccharomyces cerevisiae deletion strain KKSC1 and culture it overnight at 30°C in liquid YPD medium for 8-12 hours, and then adjust the resulting culture to OD600 nm With a value of 2.0, the culture was obtained for use.

[0023] YPD medium: yeast extract 10g / L, peptone 20g / L, glucose 20g / L.

[0024] Take the obtained culture and wild-type Saccharomyces cerevisiae strain, dilute them 5 times with distilled water as the solution respectively according to ten times the concentration, and obtain 5 cell dilution solutions with decreasing concentrations accordingly, and label them respectively for future use.

[0025] Take 3 μL of 5 diluted cell solution samples from KKSC1 and wild-type Saccharomyces cerevisiae strains, respectively, and inoculate them on SC solid medium without or with 10 mM furfural, and culture them on plates at 30°C for 48 hours.

[0026] SC so...

Embodiment 2

[0029] Example 2 Furfural resistance experiment of Saccharomyces cerevisiae deletion strain KKSC2

[0030] Take the Saccharomyces cerevisiae deletion strain KKSC2 and culture it overnight at 30°C in liquid YPD medium for 8-12 hours, and then adjust the resulting culture to OD600 nm With a value of 2.0, the culture was obtained for use.

[0031] YPD medium: yeast extract 10g / L, peptone 20g / L, glucose 20g / L.

[0032] Take the obtained culture and wild-type Saccharomyces cerevisiae strain, use distilled water as the solution, and dilute them 5 times according to the concentration of 10 times successively to obtain 5 cell dilution solutions with decreasing concentrations accordingly, and label them separately for future use.

[0033] Take 3 μL of 5 diluted cell solution samples from KKSC2 and wild-type Saccharomyces cerevisiae strains and spot them on SC solid medium without or with 10 mM furfural, and culture them on plates at 30°C for 48 hours.

[0034] SC solid medium: glucos...

Embodiment 3

[0036] Example 3 Furfural resistance experiment of Saccharomyces cerevisiae deletion strain KKSC3

[0037] Take the Saccharomyces cerevisiae deletion strain KKSC3 and culture it overnight in liquid YPD medium at 30°C for 8-12 hours, then adjust the resulting culture to OD600 nm With a value of 2.0, the culture was obtained for use.

[0038] YPD medium: yeast extract 10g / L, peptone 20g / L, glucose 20g / L.

[0039] Take the obtained culture and wild-type Saccharomyces cerevisiae strain, dilute them 5 times with distilled water as the solution respectively according to ten times the concentration, and obtain 5 cell dilution solutions with decreasing concentrations accordingly, and label them respectively for future use.

[0040] Take 3 μL of 5 diluted cell solution samples from KKSC3 and wild-type Saccharomyces cerevisiae strains, respectively, and spot them on SC solid medium without or with 10 mM furfural, and culture them on plates at 30°C for 48 hours.

[0041] SC solid medium:...

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Abstract

The invention relates to a saccharomyces cerevisiae deleted bacterial strain and application thereof in a furfural resistant aspect, provides a sieving method of the deleted bacterial strain, tests and verifies the application of the saccharomyces cerevisiae deleted bacterial strain in the furfural resistant aspect and belongs to the technical field of biological energy technology development. Three provided furfural resistant gene deleted bacterial strains can be applied to a shake flask and a fermentation tank to research the capability of the saccharomyces cerevisiae for generating ethanolthrough fermentation by utilizing a furfural-containing cellulose acidolysis solution, so that high-yield excellent genetic engineering strain is provided for the cellulose alcohol industry. In addition, the furfural resistant gene deleted bacterial strains also can be used for researching molecular mechanism of the saccharomyces cerevisiae for resisting to the furfural. The saccharomyces cerevisiae deleted bacterial strain and the application thereof in the furfural resistant aspect, disclosed by the invention, have the advantages of large scale of the sieving process and high efficiency; and the furfural resistant capability is truly improved by the sieved bacterial strains.

Description

technical field [0001] The invention relates to a deletion strain of Saccharomyces cerevisiae and its application in furfural resistance, provides a screening method for the deletion strain, verifies its application in furfural resistance, and belongs to the technical field of bioenergy technology development. Background technique [0002] With the depletion of petroleum resources, the rise of petroleum prices and the deterioration of the environment, people's demand for alternative energy and environmentally friendly energy has increased. It has become a research field in the field of industrial biotechnology to find new renewable resources to replace fossil resources and develop clean energy. hotspot. The development of biomass energy can alleviate the dependence on petroleum resources, control carbon dioxide emissions, and promote the development of new agricultural industrial chains, which is of great significance to promote the construction of new socialist countryside ...

Claims

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Application Information

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IPC IPC(8): C12N1/18C12P7/10C12R1/865
CPCY02E50/16Y02E50/10
Inventor 蒋伶活
Owner JIANGNAN UNIV