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Ex vivo screen (Biolector)

ABSTRACT: Precision Glycans Enhance Gamma-Aminobutyric Acid Production in Human Gut Model

PROVIDER: PRJNA1225188 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR33237026_1.fastq.gz	Fastqsanger.gz
	SRR33237027_1.fastq.gz	Fastqsanger.gz
	SRR33237028_1.fastq.gz	Fastqsanger.gz
	SRR33237029_1.fastq.gz	Fastqsanger.gz
	SRR33237030_1.fastq.gz	Fastqsanger.gz

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Project description:Precision Glycans Enhance Gamma-Aminobutyric Acid Production in Human Gut Model

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Project description:Purpose: High γ-aminobutyric acid (GABA)-producing Levilactobacillus brevis strain NPS-QW 145 along with Streptococcus thermophilus (one of the two starter bacteria used to make yogurt for its proteolytic activity) to enhance GABA production in milk. But a mechanistic understanding on how Levilactobacillus brevis cooperated with S. thermophilus to stimulate GABA production has been lacking. Method: Metatranscriptomic analyses combined with peptidomics were carried out to unravel the casein and lactose utilization patterns during milk fermentation with the co-culture. Results: We found particular peptides hydrolyzed by S. thermophilus 1275 were transported and biodegraded with peptidase in Lb. brevis 145 to meet the growth needs of the latter. In addition, amino acid synthesis and metabolism in Lb. brevis 145 were also activated to further support its growth. Glucose, as a result of lactose hydrolysis by S. thermophilus 1275, but not available lactose in milk, was outcompeted by Lb. brevis 145 as a main carbon source for glycolysis to produce ATP.In the stationary phase, under the acidic condition due to accumulation of lactic acid produced by S. thermophilus 1275, genes expression involved in pyridoxal phosphate (coenzyme of glutamic acid decarboxylase) metabolism and glutamic acid decarboxylase (Gad) in Lb. brevis 145 were induced for GABA production.

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