1997KRIBB RepositoryRequires access

Characterization of an endoxylanase produced by an isolated strain of Bacillus sp

Jay J. Lee, Kyung Soo Hahm, Ki Young Lee, Sung-Taik Lee

Open publisher page 10 citations

Abstract

Microorganisms producing xylanase were screened for the enzymatic production of xylo-oligosaccharides from xylan. One of the bacteria isolated from compost produced an endoxylanase extracellularly. The bacterium was identified as Bacillus sp. according to its taxonomic characteristics examined. Xylanase production reached upto 5 U/ml after 22 h of culture in LB medium at 30°C. The xylanase was purified by ammonium sulfate precipitation and gel filtration. The molecular weight of the xylanase was estimated to be 20,400 by SDS-PAGE. Optimal temperature and pH for the xylanase activity was 60°C and 6.5, respectively. The enzyme was stable at temperatures upto 40°C and pH values from 4 to 10. The xylanase was completely inhibited by the addition of 2 mM mercury ion. Apparent Km and Vmax values for oat spelt xylan were 9.2 mg/ml and 1954 U/mg protein, respectively. For birchwood xylan, the values were 6.3 mg/ml and 1009 U/mg protein. The predominant products of the xylan hydrolysis were xylobiose, xylotriose and xylotetraose, indicating that the enzyme is an endoxylanase. Upto 85% of the initially added enzyme (2 U/ml) was bound to 50 mg/ml of the insoluble fraction of oat spelt xylan after incubation at 30°C for 30 min.

About this research paper

What this paper is about

Microorganisms producing xylanase were screened for the enzymatic production of xylo-oligosaccharides from xylan. One of the bacteria isolated from compost produced an endoxylanase extracellularly. The bacterium was identified as Bacillus sp. according to its taxonomic characteristics examined. Xylanase production reached upto 5 U/ml after 22 h of culture in LB medium at 30°C. The xylanase was purified by ammonium sulfate precipitation and gel filtration. The molecular weight of the xylanase was estimated to be 20,400 by SDS-PAGE. Optimal temperature and pH for the xylanase activity was 60°C and 6.5, respectively. The enzyme was stable at temperatures upto 40°C and pH values from 4 to 10. The xylanase was completely inhibited by the addition of 2 mM mercury ion. Apparent Km and Vmax values for oat spelt xylan were 9.2 mg/ml and 1954 U/mg protein, respectively. For birchwood xylan, the values were 6.3 mg/ml and 1009 U/mg protein. The predominant products of the xylan hydrolysis were xylobiose, xylotriose and xylotetraose, indicating that the enzyme is an endoxylanase. Upto 85% of the initially added enzyme (2 U/ml) was bound to 50 mg/ml of the insoluble fraction of oat spelt xylan after incubation at 30°C for 30 min.

Why it matters

OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Microorganisms producing xylanase were screened for the enzymatic production of xylo-oligosaccharides from xylan. One of the bacteria isolated from compost produced an endoxylanase extracellularly. The bacterium was identified as Bacillus sp. according to its taxonomic characteristics examined. Xylanase production reached upto 5 U/ml after 22 h of culture in LB medium at 30°C. The xylanase was purified by ammonium sulfate precipitation and gel filtration. The molecular weight of the xylanase was estimated to be 20,400 by SDS-PAGE. Optimal temperature and pH for the xylanase activity was 60°C and 6.5, respectively. The enzyme was stable at temperatures upto 40°C and pH values from 4 to 10. The xylanase was completely inhibited by the addition of 2 mM mercury ion. Apparent Km and Vmax values for oat spelt xylan were 9.2 mg/ml and 1954 U/mg protein, respectively. For birchwood xylan, the values were 6.3 mg/ml and 1009 U/mg protein. The predominant products of the xylan hydrolysis were xylobiose, xylotriose and xylotetraose, indicating that the enzyme is an endoxylanase. Upto 85% of the initially added enzyme (2 U/ml) was bound to 50 mg/ml of the insoluble fraction of oat spelt xylan after incubation at 30°C for 30 min.

Key concepts: Xylobiose, Xylanase, Xylan, Chemistry, Ammonium sulfate precipitation, Biochemistry, Enzyme, Bacteria

Related papers

Back to paper searchBrowse research topicsOriginal source
Characterization of an endoxylanase produced by an isolated strain of Bacillus sp — Research Paper | ScholarLens