2009•Entomological ScienceRequires access

Purification and characterization of midgut α‐amylases ofEurygaster integriceps

Ali Reza Bandani, Majid Kazzazi, Mohammad Shams Mehrabadi

Open publisher page 59 citations

Abstract

Abstract In the current study, midgut α‐amylase from Sunn pest (Eurygaster integricepsPuton) (Hemiptera: Scutelleridae), one of the most serious pests of wheat and barley in the wide area of the Near and Middle East, West Asia, and many of the new independent states of central Asia, were purified and characterized. Amylase activity was detected in the midgut of the insects which were collected from both over‐wintering sites during winter and feeding insects during spring. Amylase activities in the midgut of over‐wintering and feeding insects were 5.71 and 3.43 U/mg protein, respectively. Initially, a native electrophoretic analysis ofE. integricepscrude midgut extract showed that there are two major amylase forms in the midgut. Through the sequence of ammonium sulfate precipitation, first by gel filtration chromatography (Sephadex G‐75), anion exchange chromatography (diethylaminoethylcellulose) and second by gel filtration chromatography, specific activity of α‐amylase ofE. integricepsincreased 44‐fold from approximately 3 to 133 U/mg protein. Analysis of purified amylases by sodium dodecylsulfate polyacrylamide gel electrophoresis showed that these proteins had estimated molecular masses of 49 and 52 kDa. Optimum temperature was determined to be 30–40°C. The optimum pH value was 6.5 and theKmappfor soluble starch was 0.54%.

About this research paper

What this paper is about

Abstract In the current study, midgut α‐amylase from Sunn pest (Eurygaster integricepsPuton) (Hemiptera: Scutelleridae), one of the most serious pests of wheat and barley in the wide area of the Near and Middle East, West Asia, and many of the new independent states of central Asia, were purified and characterized. Amylase activity was detected in the midgut of the insects which were collected from both over‐wintering sites during winter and feeding insects during spring. Amylase activities in the midgut of over‐wintering and feeding insects were 5.71 and 3.43 U/mg protein, respectively. Initially, a native electrophoretic analysis ofE. integricepscrude midgut extract showed that there are two major amylase forms in the midgut. Through the sequence of ammonium sulfate precipitation, first by gel filtration chromatography (Sephadex G‐75), anion exchange chromatography (diethylaminoethylcellulose) and second by gel filtration chromatography, specific activity of α‐amylase ofE. integricepsincreased 44‐fold from approximately 3 to 133 U/mg protein. Analysis of purified amylases by sodium dodecylsulfate polyacrylamide gel electrophoresis showed that these proteins had estimated molecular masses of 49 and 52 kDa. Optimum temperature was determined to be 30–40°C. The optimum pH value was 6.5 and theKmappfor soluble starch was 0.54%.

Why it matters

OpenAlex reports 59 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

Abstract In the current study, midgut α‐amylase from Sunn pest (Eurygaster integricepsPuton) (Hemiptera: Scutelleridae), one of the most serious pests of wheat and barley in the wide area of the Near and Middle East, West Asia, and many of the new independent states of central Asia, were purified and characterized. Amylase activity was detected in the midgut of the insects which were collected from both over‐wintering sites during winter and feeding insects during spring. Amylase activities in the midgut of over‐wintering and feeding insects were 5.71 and 3.43 U/mg protein, respectively. Initially, a native electrophoretic analysis ofE. integricepscrude midgut extract showed that there are two major amylase forms in the midgut. Through the sequence of ammonium sulfate precipitation, first by gel filtration chromatography (Sephadex G‐75), anion exchange chromatography (diethylaminoethylcellulose) and second by gel filtration chromatography, specific activity of α‐amylase ofE. integricepsincreased 44‐fold from approximately 3 to 133 U/mg protein. Analysis of purified amylases by sodium dodecylsulfate polyacrylamide gel electrophoresis showed that these proteins had estimated molecular masses of 49 and 52 kDa. Optimum temperature was determined to be 30–40°C. The optimum pH value was 6.5 and theKmappfor soluble starch was 0.54%.

Key concepts: Midgut, Amylase, Ammonium sulfate precipitation, Biology, Sephadex, Size-exclusion chromatography, Polyacrylamide gel electrophoresis, Starch

Related papers

Back to paper searchBrowse research topicsOriginal source
Purification and characterization of midgut α‐amylases ofEurygaster integriceps — Research Paper | ScholarLens