Designing and Cloning of the Gene Sequence Encoding Silk Fibroin Amorphous Domain

To provide materials used in investigating the relationship between amino acid compositions of silk-like protein, structure, and functions, especially the biological functions, the motif genes encoding the silk fibroin amorphous domain, SGFGPVANGGSGEASSESDFGSSGFGPVANASSGEASSESDFAG (F) were designed...

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Published in东华大学学报(英文版) Vol. 29; no. 6; pp. 489 - 492
Main Author 黄海燕 田智芳 裔洪根 杨云星 王建南
Format Journal Article
LanguageEnglish
Published College of Textile and Clothing Engineering, Soochow University, Suzhou 215021, China%College of Textile and Clothing Engineering, Soochow University, Suzhou 215021, China 2012
National Engineering Laboratory for Modern Silk, Soochow University, Suzhou 215021, China
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ISSN1672-5220

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Summary:To provide materials used in investigating the relationship between amino acid compositions of silk-like protein, structure, and functions, especially the biological functions, the motif genes encoding the silk fibroin amorphous domain, SGFGPVANGGSGEASSESDFGSSGFGPVANASSGEASSESDFAG (F) were designed and extended using a "head-to-tail" construction strategy. The designed genes were cloned into PSLFA1180FA and multimerized to form structures containing a two-timer, a four- timer, an eight-timer, and a twelve-timer. All the resulting plasmids were digested using the restriction enzyme BamI-II and the double- enzymes BgllL/HindHI. Restriction enzyme analysis and DNA sequencing revealed the motif was successfully cloned into PSLFAll80FA and mnitimerized to form a twelve-timer without eene deletion or mutation.
Bibliography:31-1920/N
HUANG Hai-yan , TIAN Zhi-fang, YI Hong-gen , YANG Yun-xing, WANG Jian-nan National Engineering Laboratory for Modem Silk, Soochow University, Suzhou 215021, China 2 College of Textile and Clothing Engineering, Soochow University, Suzhou 215021, China
To provide materials used in investigating the relationship between amino acid compositions of silk-like protein, structure, and functions, especially the biological functions, the motif genes encoding the silk fibroin amorphous domain, SGFGPVANGGSGEASSESDFGSSGFGPVANASSGEASSESDFAG (F) were designed and extended using a "head-to-tail" construction strategy. The designed genes were cloned into PSLFA1180FA and multimerized to form structures containing a two-timer, a four- timer, an eight-timer, and a twelve-timer. All the resulting plasmids were digested using the restriction enzyme BamI-II and the double- enzymes BgllL/HindHI. Restriction enzyme analysis and DNA sequencing revealed the motif was successfully cloned into PSLFAll80FA and mnitimerized to form a twelve-timer without eene deletion or mutation.
Escherichia coli; silk fibroin; amorphous domain; genecloning; DNA electrophoresis
ISSN:1672-5220