Polypeptides endowed with a larvicidal activity toward...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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C530S350000, C435S320100, C435S252300, C435S007800, C536S023200

Reexamination Certificate

active

06310035

ABSTRACT:

The subject of the invention is nucleotide sequences coding for polypeptides endowed with a larvicidal activity towards Lepidoptera.
It relates more particularly to agents, in particular nucleotide sequences, polypeptides or even vectors, or bacterial strains modified by these sequences and expressing polypeptides making it possible to prepare larvicidal compositions active against Lepidoptera, preferably against
Spodoptera littoralis
(hereafter
S.littoralis
) or
Mamestra brassicae
(hereafter designated by
M.brassicae
) or capable of transforming the plants to be treated in conferring on them this type of activity.
BACKGROUND OF THE INVENTION
It is known that most of the isolates of
B.thuringiensis
show a toxic activity with regard to larvae of more than a hundred species of Lepidoptera.
This activity results from the capacity of the strains of
B.thuringiensis
to synthesize, at the moment of sporulation, crystalline inclusions of protein nature, or &dgr;-endotoxins, under the control of one or several types of gene.
It has been shown that the activity of these polypeptides is contained in the NH
2
-terminal half or N-terminus of the protein.
The studies carried out have shown the high specificity of the &dgr;-endotoxins towards larvae of a given species.
On account of this high specificity, many species of Lepidoptera, in particular of the family of the Noctuidae, react only weakly to commercial preparations of available
B.thuringiensis.
It is so in particular for the species
S.littoralis
, a polyphagous insect which constitutes the principal parasite of cotton and other industrially important crops. Among these crops, mention should be made of maile, the castor oil plant, tobacco, the groundnut, fodder plants, such as clover or alfalfa, or also market garden produced such as the cabbage or the tomato.
Hence, one can imagine the interest of disposing of agents targeting specifically and effectively the family of the Noctuidae and in particular
S.littoralis
or
M.brassicae.
The genes for &dgr;-endotoxins hitherto identified do not code for a polypeptide preferentially active with regard to
S.littoralis.
SUMMARY OF THE INVENTION
The search by the inventors for a sequence of nucleotides coding for a polypeptide preferably active against the Noctuidae, more especially against
S.littoralis
, has led them to study the natural. isolates of two strains of
B.thuringiensis
, the larvicidal activity of which on
S.littoralis
appears to be higher than that of the industrial preparations made starting from other strains of
B.thuringiensis.
The species in question are
aizawai
7-29 and
entomocidus
6-01.
The study of these isolates has made it possible to demonstrate the existence of several genes for &dgr;-endotoxins of different structures and different specificities, of which two genes preferentially active against
P.brassicae
but not very active against the Noctuida of cotton and a gene inactive against
P.brassicae
and
S.littoralis.
By studying the total DNA of these isolates and by carrying out appropriate hybridizations, followed by the cloning of the fragments identified by hybridization, the inventors have observed that it is possible to isolate nucleotide sequences implicated in genes for &dgr;-endotoxins coding for polypeptides active, preferably, against
S.littoralis.
Thus, the aim of the invention is to provide nucleotide sequences capable of coding for at least the NH
2
-terminal part of a &dgr;-endotoxin toxic against the Noctuidae and preferably against
S.littoralis
or
M.brassicae.
It also has the aim of providing a polypeptide toxic with regard to the Noctuidae.
Furthermore, the invention relates to a procedure for obtaining such a sequence and a polypeptide showing the desired activity as well as the intermediate agents such as vectors and bacterial strains which can be utilized for obtaining the polypeptide.
In addition, the invention relates to the uses of these sequences and polypeptides for the development of larvicidal compositions with regard to the Noctuidae, in particular
S.littoralis
and for the transformation of the plants likely to be infected by these larvae.
The invention relates to a sequence of nucleotides coding for at least a part of the N-terminal region of a polypeptide toxic specifically against the larvae of Lepidoptera of the Noctuidae family, and preferably against
S.littoralis
, characterized by its capacity of hybridization with a gene capable of expressing a polypeptide toxic towards larvae of
S.littoralis.
According to another aspect of the invention, the nucleotide sequence is characterized in that it is carried by a sequence of nucleotides of about 3 kb such as obtained by in vitro genetic recombination of sequences of nucleotides of
B.thuringiensis
capable of hybridizing with probes 1, 2 and 3 of pHTA2 shown in FIG.
2
. The fragment of 3 kb corresponds more particularly to the restriction fragment HindIII-PstI.
The sequences of nucleotides of the invention are, in addition, characterized in that they contain sites in the following order: HindIII-HincII-BglII-KpnI-HindIII-PstI.
In a preferred manner, these sequences of nucleotides are obtained by in vitro genetic recombination of DNA sequences derived from at least one strain of
B.thuringiensis
. In a variant of the embodiment of the invention, two different strains of
B.thuringiensis
are utilized.
Strains of
B.thuringiensis
particularly suited for obtaining these sequences of nucleotides are the strains corresponding to
aizawai
7-29 and
entomocidus
6-01, deposited on Apr. 21, 1987 under the No. I-661 and No. I-660, respectively, with the National Collection of Cultures of Microorganisms (N.C.C.M.) in Paris.
In an advantageous manner, the sequences of nucleotides of the invention code for a polypeptide capable of forming an immunological complex with antibodies directed against polypeptides showing the larvicidal activity with regard to
S.littoralis.


REFERENCES:
patent: 5126133 (1992-06-01), Payne et al.
patent: 5188960 (1993-02-01), Payne et al.
patent: 5246852 (1993-09-01), Payne et al.
patent: 5593881 (1997-01-01), Thompson et al.
patent: 5596071 (1997-01-01), Payne et al.
patent: 5602032 (1997-02-01), Liu et al.
patent: 0 228 838 A2 (1987-07-01), None
patent: 0 295 156 B1 (1988-04-01), None
patent: 0 405 810 B1 (1991-01-01), None
Gordon-Kamm, William J. et al., “Transformation of Maize Cells and Regeneration of Fertile Transgenic Plants,”The Plant Cell,vol. 2, pp. 603-618 (Jul. 1990).
Honigman, Alik et al., “Cloning and expression of the lepidopteran toxin produced byBacillus thuringiensisvar.ThuringiensisinEscherichia coli,” Gene,vol. 42, pp. 69-77 (1986).
Jaquet, Françoise et al., “Specificity inBacillus thuringiensisDelta-Endotoxin,”Applied and Environmental Microbiology,pp. 500-504 (Mar. 1987).
Klier, André et al., “Cloning and Expression inEscherichia coliof the Crystal Protein Gene fromBacillus thuringiensisStrainaizawa7-29 and Comparison of the Structural Organization of Genes from Different Serotypes,”Molecular Biology of Microbial Differentiation,pp. 217-224 (1985).
Suggs, Sidney V. et al., “Use of synthetic oligonucleotides as hybridization probes: Isolation of cloned cDNA sequences for human &bgr;2-microglobulin,”Proc. Natl. Acad. Sci. USA,vol. 78, No. 11, pp. 6613-6617 (Nov. 1981).
Vaeck, Mark et al., “Transgenic plants protected from insect attack,”Nature,vol. 328, pp. 33-37 (Jul. 1987).
Wabiko, Hiroetsu et al., “Bacillus thuringiensisEntomocidal Protoxin Gene Sequence and Gene Product Analysis,”DNA,vol. 5, No. 4, 1986, pp. 305-314 (1986).
Wong, Hing Cheung et al., “Transcriptional and Translational Start Sites for theBacillus thuringiensisCrystal Protein Gene,”J. of Biological Chemistry,vol. 258, No. 3, pp. 1960-1967 (Feb. 10, 1983).

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