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1.
J Gen Appl Microbiol ; 63(4): 222-227, 2017 Sep 05.
Article in English | MEDLINE | ID: mdl-28680004

ABSTRACT

The tea mosquito bug (TMB), Helopeltis spp. (Hemiptera: Miridae) is an insidious pest that poses a significant economical threat to tea plantations. Pseudomonas cultures are being used extensively for pest management which, however, resulting in a low mortality rate of insects and which has prompted us to search for a new microbial metabolite for TMB control. A chitinase purified from P. fluorescens and partially characterized by our group showed insecticidal activity against TMB. The mode of action behind chitinase toxicity is the enzymatic hydrolysis of chitin, which is a common constituent of the insect exoskeleton and gut lining of the peritrophic membrane. A chitinase-secreting strain MP-13 was characterized based on 16S rRNA sequencing and validated as Pseudomonas fluorescens. In the present study, purified chitinase (0.048 units/ml) enzyme from P. fluorescens MP-13 revealed 100% TMB mortality under in-vitro conditions. The results of this study can be utilized for future crop improvement programs and integrated pest management strategies.


Subject(s)
Bacterial Proteins/pharmacology , Chitinases/pharmacology , Heteroptera/drug effects , Insecticides/pharmacology , Pseudomonas fluorescens/enzymology , Animals , Chitin/metabolism , Chitinases/toxicity , Insecticides/toxicity , Pest Control, Biological , Pseudomonas fluorescens/classification , RNA, Ribosomal, 16S/genetics
2.
Pestic Biochem Physiol ; 116: 1-12, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25454515

ABSTRACT

An extracellular chitinase was identified and purified (CS1 and CS2) from Bacillus subtilis. The 16S rRNA sequencing was submitted in GenBank (accession numbers KC336487 and KC412256). The purified crude enzymes were identified through matrix-assisted laser desorption/ionization time-of-flight/time-of-flight mass spectrometry (MALDI-TOF MS) analysis. The peptide sequences were matched with chitinase sequences. The peak m/z with 1297. 592 and 3094.570 mascot search resulted sequence was blasted with NCBI protein sequences and confirmed that it is a chitinase enzyme. The effects of chitinase on gut enzymes lactate dehydrogenase, acid phosphatase, alkaline phosphatase and adenosine triphosphatase of the tobacco cutworm Spodoptera litura larvae were investigated. At all concentrations tested, chitinase decreased the activities of these gut enzymes relative to the control. When chitinase treated leaves were fed to larvae in bioassays, gut tissue and gut enzymes were affected. The histological study clearly shows the chitinase treated larval gut, peritrophic membrane and epithelial cells were affected significantly. Chitinase isolated from B. subtilis has effectively reduced the gut enzyme activity and growth of S. litura. The chitin based bioformulation may serve as an effective biocide against the polyphagous pest like S. litura.


Subject(s)
Bacillus subtilis/enzymology , Chitinases/toxicity , Gastrointestinal Tract/drug effects , Insecticides/toxicity , Spodoptera/drug effects , Acid Phosphatase/metabolism , Adenosine Triphosphatases/metabolism , Alkaline Phosphatase/metabolism , Amino Acid Sequence , Animals , Bacillus subtilis/genetics , Base Sequence , Chitinases/chemistry , Chitinases/genetics , Chitinases/isolation & purification , Gastrointestinal Tract/enzymology , Insect Proteins/metabolism , L-Lactate Dehydrogenase/metabolism , Larva/drug effects , Larva/enzymology , Larva/growth & development , Molecular Sequence Data , RNA, Bacterial/analysis , RNA, Ribosomal, 16S/analysis , Sequence Analysis, Protein , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Spodoptera/enzymology , Spodoptera/growth & development
3.
J Microbiol ; 48(5): 706-8, 2010 Oct.
Article in English | MEDLINE | ID: mdl-21046352

ABSTRACT

Coprinellus congregatus generates several chitinases during its entire life cycle: at the growing hyphal stage and at the mushroom autolysis stage. We have isolated a chitinase gene (chi1) from the mushroom tissue at the autolysing stage, and constructed a chitinase expression vector to get large amount of enzyme protein. Chitinase 1 (chi1) cDNA was heterologously expressed in Saccharomyces cerevisiae by gal1 promoter. The transformants showed no specific change in growth characteristics under normal growth conditions. However the expression of the gene by the gal1 promoter in the yeast transformants resulted in complete growth inhibition, while laccase expression by the gal1 promoter showed normal growth. The chitinase activities from the transformants were also more than 3 times higher than that of the recipient strain, and the chitinase expression by the real time-PCR also showed increased expression of the chi1 in the yeast transformant. Expression of a chitinase which was produced at the mushroom autolysing stage of C. congregatus resulted in yeast growth inhibition.


Subject(s)
Agaricales/enzymology , Chitinases/biosynthesis , Chitinases/toxicity , Growth Inhibitors/biosynthesis , Growth Inhibitors/toxicity , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/genetics , Agaricales/genetics , Chitinases/genetics , Cloning, Molecular , Gene Expression , Gene Expression Profiling , Growth Inhibitors/genetics , Laccase/biosynthesis , Laccase/genetics , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Recombinant Proteins/genetics , Recombinant Proteins/toxicity , Reverse Transcriptase Polymerase Chain Reaction , Transformation, Genetic
4.
Biosci Biotechnol Biochem ; 67(1): 221-4, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12619703

ABSTRACT

We investigated whether a plant chitinase can be used as a biocontrol agent instead of chemical fungicides by spraying chitinase E (family 19; class IV) from a yam (Dioscorea opposita Thunb) alone or together with beta-1,3-glucanase directly onto the surface of a powdery mildew infecting strawberry berries and leaves. Results were observed by eye and with a scanning electron microscope. The powdery mildew infecting the strawberries was degraded, mainly by the chitinase, and the disease did not appear again for more than 2 weeks. These results indicated that this kind of plant chitinase might be safe and biodegradable biocontrol agent for use instead of conventional fungicides.


Subject(s)
Chitinases/toxicity , Dioscorea/enzymology , Fungicides, Industrial , Pest Control, Biological , Chitinases/isolation & purification , Fragaria , Hydrolases/toxicity , Microscopy, Electron, Scanning , Plant Diseases/microbiology
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