An effective family shuffling method using single-stranded DNA

被引:53
作者
Kikuchi, M [1 ]
Ohnishi, K [1 ]
Harayama, S [1 ]
机构
[1] Marine Biotechnol Inst, Kamaishi, Iwate 0260001, Japan
关键词
family shuffling; nahH; protein evolution; single-stranded DNA; xylE;
D O I
10.1016/S0378-1119(99)00547-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Family shuffling, which is one of the most powerful techniques for in vitro protein evolution, always involves the problem of reassembling the gene fragments into parental gene sequences, because such a process prevents the formation of chimeric sequences. In order to improve the efficiency of hybrid formation in family shuffling, single-stranded DNAs (ssDNAs) were used as templates. The ssDNAs of two catechol 2,3-dioxygenase genes, nahH and xylE, were prepared, the xylE strand being complementary to the nahH strand. When these ssDNAs were digested by DNase I and reassembled, chimeric genes were obtained at a rate of 14%, which was much higher than the rate of less than 1% obtained by shuffling with double-stranded DNAs. Chimeric catechol 2,3-dioxygenases that were more thermally stable than the parental enzymes, XylE and NahH, were obtained by this ssDNA-based DNA shuffling. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:133 / 137
页数:5
相关论文
共 17 条
[1]   Evolution of a cytokine using DNA family shuffling [J].
Chang, CCJ ;
Chen, TT ;
Cox, BW ;
Dawes, GN ;
Stemmer, WPC ;
Punnonen, J ;
Patten, PA .
NATURE BIOTECHNOLOGY, 1999, 17 (08) :793-797
[2]   Improved green fluorescent protein by molecular evolution using DNA shuffling [J].
Crameri, A ;
Whitehorn, EA ;
Tate, E ;
Stemmer, WPC .
NATURE BIOTECHNOLOGY, 1996, 14 (03) :315-319
[3]   Molecular evolution of an arsenate detoxification pathway DNA shuffling [J].
Crameri, A ;
Dawes, G ;
Rodriguez, E ;
Silver, S ;
Stemmer, WPC .
NATURE BIOTECHNOLOGY, 1997, 15 (05) :436-438
[4]   DNA shuffling of a family of genes from diverse species accelerates directed evolution [J].
Crameri, A ;
Raillard, SA ;
Bermudez, E ;
Stemmer, WPC .
NATURE, 1998, 391 (6664) :288-291
[5]   Evolution of differential substrate specificities in Mu class glutathione transferases probed by DNA shuffling [J].
Hansson, LO ;
Bolton-Grob, R ;
Massoud, T ;
Mannervik, B .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 287 (02) :265-276
[6]   Artificial evolution by DNA shuffling [J].
Harayama, S .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (02) :76-82
[7]   Novel family shuffling methods for the in vitro evolution of enzymes [J].
Kikuchi, M ;
Ohnishi, K ;
Harayama, S .
GENE, 1999, 236 (01) :159-167
[8]   Enhanced degradation of polychlorinated biphenyls by directed evolution of biphenyl dioxygenase [J].
Kumamaru, T ;
Suenaga, H ;
Mitsuoka, M ;
Watanabe, T ;
Furukawa, K .
NATURE BIOTECHNOLOGY, 1998, 16 (07) :663-666
[9]  
MELGAR E, 1968, J BIOL CHEM, V243, P4409
[10]   Strategies for the in vitro evolution of protein function: Enzyme evolution by random recombination of improved sequences [J].
Moore, JC ;
Jin, HM ;
Kuchner, O ;
Arnold, FH .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 272 (03) :336-347