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In vitro digestive properties and the bioactive effect of walnut green husk on human gut microbiota
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Introduction
Walnut green husk (WGH) is a waste byproduct from walnut industry. However, it is not well-known about its bioactive effect on human gut health.
Methods
This study conducted
in vitro
digestion and fermentation experiments to study the bioactive effect of WGH.
Results
Microbial fermentation was the primary mechanism to efficiently release phenolics and flavonoids, resulting in more excellent antioxidant capacities (DPPH, ABTS, and FRAP assays), which reached a highest value with 14.82 ± 0.01 mg VcE/g DW, 3.47 ± 0.01 mmol TE/g DW, and 0.96 ± 0.07 mmol FeSO
4
·7H
2
O/g DW, respectively. The surface microstructure of WGH became loose and fragmented after microbial fermentation. The analytical results of gut microbiota demonstrated that WGH could significantly increase the relative abundance of Proteobacteria in phylum level and
Phascolarctobacterium
in genus level while certain pro-inflammatory bacteria (such as
Clostridium_sensu_stricto_1, Dorea
,
Alistipes
, and
Bilophila
) was inhibited. Additionally, 1,373 differential metabolites were identified and enriched in 283 KEGG pathways. Of which some metabolites were significantly upregulated including ferulic acid, chlorogenic acid, umbelliferone, scopolin, muricholic acid, and so forth.
Discussion
These results indicated that WGH could have antioxidant and anti-inflammatory activities in the human gut, which could improve the economical value of WGH in the food industry.
Title: In vitro digestive properties and the bioactive effect of walnut green husk on human gut microbiota
Description:
Introduction
Walnut green husk (WGH) is a waste byproduct from walnut industry.
However, it is not well-known about its bioactive effect on human gut health.
Methods
This study conducted
in vitro
digestion and fermentation experiments to study the bioactive effect of WGH.
Results
Microbial fermentation was the primary mechanism to efficiently release phenolics and flavonoids, resulting in more excellent antioxidant capacities (DPPH, ABTS, and FRAP assays), which reached a highest value with 14.
82 ± 0.
01 mg VcE/g DW, 3.
47 ± 0.
01 mmol TE/g DW, and 0.
96 ± 0.
07 mmol FeSO
4
·7H
2
O/g DW, respectively.
The surface microstructure of WGH became loose and fragmented after microbial fermentation.
The analytical results of gut microbiota demonstrated that WGH could significantly increase the relative abundance of Proteobacteria in phylum level and
Phascolarctobacterium
in genus level while certain pro-inflammatory bacteria (such as
Clostridium_sensu_stricto_1, Dorea
,
Alistipes
, and
Bilophila
) was inhibited.
Additionally, 1,373 differential metabolites were identified and enriched in 283 KEGG pathways.
Of which some metabolites were significantly upregulated including ferulic acid, chlorogenic acid, umbelliferone, scopolin, muricholic acid, and so forth.
Discussion
These results indicated that WGH could have antioxidant and anti-inflammatory activities in the human gut, which could improve the economical value of WGH in the food industry.
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