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Complete genome sequence of Bacillus pumilus NWMCC0302, a strain for degrading bovine blood
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Abstract
Background
Directly discharging livestock and poultry slaughter blood without proper treatment can cause severe ecological damage. Exploring the use of microorganisms to break down waste blood into smaller molecules such as peptides and amino acids, as well as investigating the possibility of transforming these small molecules into water-soluble fertilizers containing amino acids, holds significant research value in the comprehensive utilization of livestock and poultry blood.
Results
In this study, a single strain of Bacillus pumilus NWMCC0302, which has effectively degraded bovine blood, was isolated from abattoir blood sludge using casein agar plates and Columbia blood agar plates. The degradation test was carried out using bovine raw blood as a nitrogen source in the medium, and the results showed that the strain degraded 53.83% of bovine blood under optimal degradation conditions. The whole genome sequencing of Bacillus pumilus NWMCC0302 was conducted using the second-generation DNBSEQ platform and the third-generation PacBio platform, employing high-throughput sequencing technology. The size of the strain's entire genome was determined to be 3 868 814 bp with a G-C content of 41.63%. The total gene length accounted for 88.98% of the genome length at 3 442 341 bp and encoded 4 113 genes. The strain contained 79 tRNAs, 24 rRNAs, 7 sRNAs, and 296 repetitive sequences. The gene data obtained from sequencing were also functionally annotated using the COG, KEGG, and VFDB databases. In the COG database, 310 genes were involved in amino acid transport and metabolism, including 10 catabolic proteins related to COGs. In the KEGG database, were 201 genes involved in amino acid metabolism pathways, including 8 genes in nitrogen metabolism pathways and 2 genes in oxidative pathways. The VFDB database contains two lysostaphin genes and one serine protease-hydrolyzed ClpP gene.
Conclusions
In summary, Bacillus pumilus NWMCC0302 was screened for its efficient ability to degrade bovine blood. Additionally, the genetic information of Bacillus pumilus NWMCC0302 was revealed at the genetic level, providing a feasible experimental method for applying this strain to the degradation of blood from slaughtered livestock and poultry. Moreover, it is a potential functional strain for producing amino acid-containing water-soluble fertilisers.
Springer Science and Business Media LLC
Title: Complete genome sequence of Bacillus pumilus NWMCC0302, a strain for degrading bovine blood
Description:
Abstract
Background
Directly discharging livestock and poultry slaughter blood without proper treatment can cause severe ecological damage.
Exploring the use of microorganisms to break down waste blood into smaller molecules such as peptides and amino acids, as well as investigating the possibility of transforming these small molecules into water-soluble fertilizers containing amino acids, holds significant research value in the comprehensive utilization of livestock and poultry blood.
Results
In this study, a single strain of Bacillus pumilus NWMCC0302, which has effectively degraded bovine blood, was isolated from abattoir blood sludge using casein agar plates and Columbia blood agar plates.
The degradation test was carried out using bovine raw blood as a nitrogen source in the medium, and the results showed that the strain degraded 53.
83% of bovine blood under optimal degradation conditions.
The whole genome sequencing of Bacillus pumilus NWMCC0302 was conducted using the second-generation DNBSEQ platform and the third-generation PacBio platform, employing high-throughput sequencing technology.
The size of the strain's entire genome was determined to be 3 868 814 bp with a G-C content of 41.
63%.
The total gene length accounted for 88.
98% of the genome length at 3 442 341 bp and encoded 4 113 genes.
The strain contained 79 tRNAs, 24 rRNAs, 7 sRNAs, and 296 repetitive sequences.
The gene data obtained from sequencing were also functionally annotated using the COG, KEGG, and VFDB databases.
In the COG database, 310 genes were involved in amino acid transport and metabolism, including 10 catabolic proteins related to COGs.
In the KEGG database, were 201 genes involved in amino acid metabolism pathways, including 8 genes in nitrogen metabolism pathways and 2 genes in oxidative pathways.
The VFDB database contains two lysostaphin genes and one serine protease-hydrolyzed ClpP gene.
Conclusions
In summary, Bacillus pumilus NWMCC0302 was screened for its efficient ability to degrade bovine blood.
Additionally, the genetic information of Bacillus pumilus NWMCC0302 was revealed at the genetic level, providing a feasible experimental method for applying this strain to the degradation of blood from slaughtered livestock and poultry.
Moreover, it is a potential functional strain for producing amino acid-containing water-soluble fertilisers.
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