2021
DOI: 10.3390/ijms22073523
|View full text |Cite
|
Sign up to set email alerts
|

High Diversity of β-Glucosidase-Producing Bacteria and Their Genes Associated with Scleractinian Corals

Abstract: β-Glucosidase is a microbial cellulose multienzyme that plays an important role in the regulation of the entire cellulose hydrolysis process, which is the rate-limiting step in bacterial carbon cycling in marine environments. Despite its importance in coral reefs, the diversity of β-glucosidase-producing bacteria, their genes, and enzymatic characteristics are poorly understood. In this study, 87 β-glucosidase-producing cultivable bacteria were screened from 6 genera of corals. The isolates were assigned to 21… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
5
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 14 publications
(6 citation statements)
references
References 61 publications
1
5
0
Order By: Relevance
“…The most relative abundance genes in CAZyme were the GH, followed by GT, then CBM, and then CE, and AA and Pl were the least abundance. The above results were found to agree with previous studies [68,69]. The GH comprises a large group of enzymes responsible for polysaccharide metabolism such as chitin, cellulose, xylan and starch [70].…”
Section: Discussionsupporting
confidence: 92%
“…The most relative abundance genes in CAZyme were the GH, followed by GT, then CBM, and then CE, and AA and Pl were the least abundance. The above results were found to agree with previous studies [68,69]. The GH comprises a large group of enzymes responsible for polysaccharide metabolism such as chitin, cellulose, xylan and starch [70].…”
Section: Discussionsupporting
confidence: 92%
“…In September 2017, coral fragments (approximately 10 × 10 cm 2 ) were collected from seven healthy corals using a hammer and punch at a depth of 2–10 m. The collected samples were gently washed with sterile seawater and placed in sterile plastic bags. All samples were stored at low temperatures (0–4 °C) to reduce mucus secretion and were immediately transported to the laboratory for bacterial isolation according to our previous research 31 . Subsequently, pure strains were transferred to screening plates (dextrose marmite agar solid plates supplemented with 0.05% esculin) and incubated at 28 °C until a dark zone appeared surrounding the colony border.…”
Section: Methodsmentioning
confidence: 99%
“…All samples were stored at low temperatures (0-4 °C) to reduce mucus secretion and were immediately transported to the laboratory for bacterial isolation according to our previous research. 31 Subsequently, pure strains were transferred to screening plates (dextrose marmite agar solid plates supplemented with 0.05% esculin) and incubated at 28 °C until a dark zone appeared surrounding the colony border. The positive colonies were separately cultured in dextrose marmite without agar at 28 °C and then mixed together for extraction of the total genomic DNA, according to the reported method with minor modifications.…”
Section: Strains Vectors and Reagentsmentioning
confidence: 99%
“…Fibrolytic enzymes are a system of three different enzymes, namely, endoglucanase, exoglucanase, and β-glucosidase (Srivastava et al, 2019). β-glucosidase is the final enzyme in fiber degradation, which decides the rate of the total conversion of fiber into glucose (Harhangi et al, 2002;Su et al, 2021;Zhang et al, 2019).…”
Section: Introductionmentioning
confidence: 99%
“…Fibrolytic enzymes are a system of three different enzymes, namely, endoglucanase, exoglucanase, and β‐glucosidase (Srivastava et al, 2019). β‐glucosidase is the final enzyme in fiber degradation, which decides the rate of the total conversion of fiber into glucose (Harhangi et al, 2002; Su et al, 2021; Zhang et al, 2019). Therefore, the digestibility of fiber might be improved by introducing the β‐glucosidase gene ( BGL ) into swine with stable and efficient expression through biotechnological methods.…”
Section: Introductionmentioning
confidence: 99%