首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Construction and expression of synthetic DNA fragments coding for polypeptides with elevated levels of essential amino acids
Authors:J M Jaynes  P Langridge  K Anderson  C Bond  D Sands  C W Newman  R Newman
Institution:(1) Department of Biochemistry, Louisiana State University, 70803 Baton Rouge, LA, USA;(2) Department of Agricultural Biochemistry, Waite Agricultural Research Institute, 5064 Glen Osmond, South Australia, Australia;(3) Department of Microbiology, Montana State University, 59717 Bozeman, MT, USA;(4) Department of Plant Pathology, Montana State University, 59717 Bozeman, MT, USA;(5) Department of Animal Sciences, Montana State University, 59717 Bozeman, MT, USA;(6) Department of Home Economics, Montana State University, 59717 Bozeman, MT, USA
Abstract:Summary Polypeptides, with elevated levels of essential amino acids, could be useful as partial protein supplements to food and feeds. To obtain DNA fragments coding for these polymers, oligonucleotides were constructed by random synthesis of a mixture of appropriate codon pairs and inserted into a bacterial plasmid in E. coli. Two of the isolated fragments were subjected to DNA sequence analysis and theoretically code for polypeptides containing up to 23% lysine, 12% tryptophan, 12% methionine, 6% isoleucine, and 6% threonine. These five amino acids make up 60% of the total amino acid content of the peptide, compared with 25% for the same amino acids in agr lactalbumin, a milk protein considered to be high in essential amino acids. These fragments, when fused to an active bacterial promoter, which directs the synthesis of chloramphenicol acetyl transferase (CAT), cause bacteria, harboring these modified genes, to take up more lysine as compared to control cells and produce commensurately larger CAT polypeptides. This method of gene synthesis may permit production of polypeptides with a specified amino acid composition to supplement specific diets low in the essential amino acids.
Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号