Bacillus Thuringiensis Spodoptera Litura Solanum Lycopersicum
Bacillus Thuringiensis Spodoptera Litura Solanum Lycopersicum
Bacillus Thuringiensis Spodoptera Litura Solanum Lycopersicum
2018
Akhmad Rizali*
Abstract
Tomato plants are horticultural commodities that can provide benefits to farmers, beside the market demand
that continues to increase, the cultivation method is easy. Tomatoes are also one type of vegetable plant that
contains many vitamins and proteins that have been known by elderly people. Numerous chemical insecticides
have been used in order to control pests, which damage for agriculture. While they are too expensive in the
developing countries and harmful to both human and the environment. In addition, target insect pests rapidly
develop biological resistance especially at higher rates of application. The chemical insecticides are still
contributing to human life enormously, but they have been distributed in ecological system of organisms
including human beings because of their low specific toxicity to any organism and their low specific toxicity to
any organism and their slight decomposition in nature. An alternative control is needed with microbial
insecticide which is using B. thuringiensis B. thuringiensis used in this study is B. thuringiensis which is already
commercial.Then carried out purification as follows B. thuringiensis concentration of 5g per liter of water, 10g
per liter of water, 15g per liter of water, 20g per liter of water. In treatment B. thuringiensis10g per liter of water
can stop eating at 2 hours after application, and has been able to control as much as 75 percent.
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placed in one tray. The some procedure was followed Results and discussion
for the third and forth instar larvae. The larvae were Stop feeding
provided daily with fresh cabbage leaves. Three- to Based on the test results on stop feeding, it was
four-day old larvae of the insect were transferred into shown that the application of B. thuringensis at a
separate rearing trays thickly lined with tissue paper concentration of 10g per liter of water was not
with soil on top which served as pupation sites. The significantly different from the treatment of B.
pupae were collected and kept in clean petri dishes thuringiensis 15g per liter of water and 20g per liter
until emergence. From this rearing, there were 200 of water but very different from the treatment of 5g
instars 3 used as experimental material, then the per liter of water and 0g per liter of water (Table 1.). In
larvae were fasted for 3 days and then infested with the results of the observation shown that B.
10 larvae to tomato plants. After B. thuringiensis thuringiensis 10g perliter of water was able to stop
application by spraying on experimental plants. eating all armyworm at 2, 3, 4, 5, 6, and 7 hour after
application, and this procedure is followed in B.
Growing Media thuringiensis of 15 and 20g per liter of water. this is
Planting media transfer into small polybags 8x9cm cause by gave concentration of medium doses to high
size, then F1 varieties of tomato seeds sown into doses at the treatment. It is possible that the number of
polybags that have been filled with media, after that spores consumed by the test insect is more rapid and
the seeds that are 1 week old can be cultured on the developing in their body. Causing the larva to stop
bag that has been prepared as treatment material. eating due to poisoning. Steinkraus et al. (2018), Spray
table tests with B. thuringiensis (Javelin WG on wheat
The cage is made of gauze with a wire frame, the size leaves against armyworm, Pseudaletia unipuncta
of the cage is 30x100cm, the gauze cage is used to showed that 1st and 3rd instars had LC50s of 0.09 and
cover polybags containing tomato plants, in order to 0.55kg per ha, respectively, 7d after treatment, at the
prevent that attack of other plant pest organisms. higher rate stop feeding and mortality at 2 days 76%
Symtomatology Mortality
Observation on of B. thuringiensis from tomato Based on observations showing that B. thuringiensis
plants on armyworms showed that infected insect from 1-7 days after application had a significant effect
larvae turned yellowish at the middle and hind parts on larval mortality. On 2 days after the B.
of the abdomen (Fig. 1B). The integument also turned thuringiensis treatment, concentration of 10g per liter
brown to black as the infection progressed and the of water can kill 75% of the armyworm larva, followed
body became sticky because of oral and anal by treatment on the the third day to the seven days
discharges. Dead larvae become shrunken and later after application (Table 2.). Giving B. thuringiensis
turned black with putrid odor (Rizali, 2017). with a concentration of 10, 15, and 20g per liter of
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Delucca AJII, Simonson JG, Larson AD. 1981. Ishii, T, Ohba M. 2013. Investigation of mosquito-
Bacillus thuringiensis distribution in soils of the specific larvicidal activity of a soil isolate of Bacillus
United States.Canadian J. Maicrobiol 27, 865-870. thuringiensi serovar Canadensis. Curr. Microbiol
35, 40-43.
Dulmage HT. 1992. Insecticidal activity of Bacillus
thuringiensis and their potential for pest control in Kalman S, Kiehne KK, Libs JL, Yamamoto T.
Microbial control for pests and plant diseases and 1993. Cloning of novel cry IC-type gene from a strain
plant diseases 1970-1980 (Ed.H.D Burges). Acad. Bacillus thuringiensis subs. Galleriae. Appl. Enviro.
Press. N.Y. PP. Microbio 59, 1131-1137.
Golberg LJ, Margalit J. 1977. A bacterial spore Kawalek MD, Benjamin S, Lee HL, Gill SS.
demonstrating rapid larvicidal activity against 1995. Isolation and identification of novel toxin from
Anopheles sergentii, Uranotaeniaunguiculata, a new mosquitocidal isolate from Malaysia, Bacillus
Culexunivitattus, Aedesaegypti and Culexpipiens, thuringiensis subsp. Jegathesan. Apl. Enviro.
Mosq. New 37, 355-358. Microbiol 2965-2969.
Held GA, Kawanishi CY, Huang YS. 1990. Laemmli UK. 1970. Cleavage of structural proteins
Characterization of the parasporal inclusion of Bacillus during tha assembly of the head of bacteriophage T4.
thuringiensis subsp. Kyushuensis. J. Bacteriol. 481-483. Nature (London) 277, 680-685).
Iizuka T, Ishino M, Nakajima T. 1982. Comparative Lee SG, Eckblad W, Bulla LA. 1985. Diversity of
morphology of Parasporal crystal and characterization of protein inclusion bodies and identification of
plasmid DNA from various subspecies of mosquitocidal protein in Bacillus thuringiensis
entomopathogenic bacteria, Bacillus thuringiensis. J. subsp. Israelensis. Biochem. Biophys. Res. Commun
Fac. Agric. Hokkaido Univ 13, 423-431. 126, 953-960.
Iizuka T, Sasaki J, Asano S, Bando H. 1995. Lopez-Pazos SA, Martinez JM, Castilo AX,
Comparative studies on isolation and identification of Samanca JAC. 2009. Present and significant of
Bacillus thuringiensis. Biotechnology and Enviro. Bacillus thuringiensis Cry proteins associated with
Benefits, Vol I, 143-153. the Andean weevil Premnotry pesvorax (Coleotera:
Curculionidae).
Iizuka T, Yamamoto T. 1984. Serological
properties of the mosquitocidal protein of Bacillus Ohba M, Aizawa K. 1986. Insect toxicity of Bacillus
thuringiensis and the morphology of its parasoral thuringiensis isolated from soils of Japan. J.
crystal. J. fac. Hokkaido Univ 62, 98-114. Invertebr. Pathol 47, 12-20.
122 | Rizali
J. Bio. & Env. Sci. 2018
Padua LE, Ohba M, Aizawa K. 1984. Isolation of a Rizali A. 2017. Occurrence of Bacillus thuringiensis
Bacillus thuringiensis strain (serotype 8a:8b) highly from different plant areas on South Kalimantan,
and selectively toxic against mosqouito larvae. J. Indonesia. JBES 11(6), 53-58.
Invertebr. Pathol 44, 12-17.
Poopathi S, Abidha S. 2010. Mosquitocidal Syukur M, Helfi ES, Rudi H. 2015. Planting
bacterial toxin (Bacillus spaeharicusand Bacillus
tomatoes in the rainy season. Jakarta.
thuringiensis serovar israelensis): mode of action,
cytopathological effects and mechanism of resistance.
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