Regulation of cry Gene Expression in Bacillus thuringiensis

被引：45

作者：

Deng, Chao ^{[1
,2
]}

Peng, Qi ^{[1
]}

Song, Fuping ^{[1
]}

Lereclus, Didier ^{[2
,3
]}

机构：

[1] Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China

[2] INRA, Micalis UMR 1319, F-78280 La Miniere, Guyancourt, France

[3] AgroParisTech, UMR Micalis, F-78352 Jouy En Josas, France

来源：

TOXINS | 2014年 / 6卷 / 07期

基金：

中国国家自然科学基金;

关键词：

cry gene; transcription; metabolism; crystallization; protein expression; regulation; RNA stability; INSECTICIDAL CRYSTAL PROTEINS; CATABOLITE-RESPONSIVE ELEMENT; DELTA-ENDOTOXIN PRODUCTION; CRYIIIA TOXIN GENE; SUBSP ISRAELENSIS; ESCHERICHIA-COLI; MESSENGER-RNA; 20-KILODALTON PROTEIN; 20-KDA PROTEIN; TRANSCRIPTIONAL REGULATION;

D O I：

10.3390/toxins6072194

中图分类号：

TS2 [食品工业];

学科分类号：

0832 ;

摘要：

Bacillus thuringiensis differs from the closely related Bacillus cereus group species by its ability to produce crystalline inclusions. The production of these crystals mainly results from the expression of the cry genes, from the stability of their transcripts and from the synthesis, accumulation and crystallization of large amounts of insecticidal Cry proteins. This process normally coincides with sporulation and is regulated by various factors operating at the transcriptional, post-transcriptional, metabolic and post-translational levels.

引用

页码：2194 / 2209

页数：16

共 79 条

[1] A 20-KILODALTON PROTEIN IS REQUIRED FOR EFFICIENT PRODUCTION OF THE BACILLUS-THURINGIENSIS SUBSP ISRAELENSIS 27-KILODALTON CRYSTAL PROTEIN IN ESCHERICHIA-COLI [J].

ADAMS, LF ;

VISICK, JE ;

WHITELEY, HR .

JOURNAL OF BACTERIOLOGY, 1989, 171 (01) :521-530

[2] HOW DOES BACILLUS-THURINGIENSIS PRODUCE SO MUCH INSECTICIDAL CRYSTAL PROTEIN [J].

AGAISSE, H ;

LERECLUS, D .

JOURNAL OF BACTERIOLOGY, 1995, 177 (21) :6027-6032

[3] STAB-SD: A Shine-Dalgarno sequence in the 5' untranslated region is a determinant of mRNA stability [J].

Agaisse, H ;

Lereclus, D .

MOLECULAR MICROBIOLOGY, 1996, 20 (03) :633-643

[4] STRUCTURAL AND FUNCTIONAL-ANALYSIS OF THE PROMOTER REGION INVOLVED IN FULL EXPRESSION OF THE CRYIIIA TOXIN GENE OF BACILLUS-THURINGIENSIS [J].

AGAISSE, H ;

LERECLUS, D .

MOLECULAR MICROBIOLOGY, 1994, 13 (01) :97-107

[5] EXPRESSION IN BACILLUS-SUBTILIS OF THE BACILLUS-THURINGIENSIS CRYIIIA TOXIN GENE IS NOT DEPENDENT ON A SPORULATION-SPECIFIC SIGMA-FACTOR AND IS INCREASED IN A SPO0A MUTANT [J].

AGAISSE, H ;

LERECLUS, D .

JOURNAL OF BACTERIOLOGY, 1994, 176 (15) :4734-4741

[6]

AHN KH, 1990, J BIOL CHEM, V265, P11734

[7]

AKIYAMA M, 1993, J BIOL CHEM, V268, P633

[8]

Ali NO, 2001, J BACTERIOL, V183, P2497

[9] CONSTRUCTION OF CLONING VECTORS FOR BACILLUS-THURINGIENSIS [J].

ARANTES, O ;

LERECLUS, D .

GENE, 1991, 108 (01) :115-119

[10] Sporulation and δ-endotoxin synthesis by Bacillus thuringiensis [J].

Aronson, A .

CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (03) :417-425

← 1 2 3 4 5 6 7 8 →