E. rhapontici
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Transcript E. rhapontici
Dyah Anindita Asriwulan
10605111
herbicola
amylovora
Erwinia
carotovora
: Erwinia
rhapontici
Atypical
erwinias
Facultative anaerobic bacteria
Gram negative
Usually single
Non-spore forming
Non-capsulated
Rods (0,5-0,8 x 1,2-1,5 µ)
Motile by several
Peritrichous flagella
G-C content of DNA : 51,0-53,1 %
Antibiotic
sensitivity : erythromycin, aureomycin, chloramphenicol,
streptomycin, terramycin, tetracycline, and dimethyl chlorotetracycline
Distinguish from other non-pectolytic species of Erwinia in the carotovora
group : falilure to grow at 37°C, inability to produce gas from glucose,
inhibition by KCN, production of acetoin, ability to reduce sucrose, and
production of acid from raffinose, melezitose, dulcitol, and lactose
API test
+
-
Erwinia rhapontici
Fementation of glucose, sucrose, arabinose, fructose, maltose, rhamnose, galactose,
mannose, sorbitol, glycerol, inositol, melibiose, and amygladin. Catalase, βgalactosidase, acetoin production, citrate utilization, nitrate reduction, esculin
hydrolysis.
Growth at 37°C, production of oxidase, hydrogen sulfide, urease, argenine dihydrolase,
lysine and ornithine decarboxilase, tryptophan deaminase, indole, gelatin hydrolysis,
gas production from glucose, starch fermentation.
E. rhapontici is able to convert sucrose into isomaltulose (palatinose, 6-
O-alpha-D-glucopyranosyl-D-fructose) and thehalulose (1-O-alpha-Dglucopyranosyl-D-fructose) by the activity of a sucrose isomerase.
Isomaltulose (commonly referred to as palatinose, 6-O-a-Dglucopyranosyl-D-fructose) and trehalulose (1-O-a-D-glucopyranosylD-fructose) are functional isomers of sucrose.
The adaptive role of sucrose isomer formation is unclear.
Many bacteria have evolved biochemical systems for the production
of storage compounds that serve as reserve material. These storage
compounds become especially important under conditions of limited
nutrient supply. Therefore, it was suspected that the bio-conversion of
sucrose may be a method of irreversibly sequestering a carbon
and energy source in a form unavailableto competitors such as the host
plant or other microorganisms
The formation of sucrose isomers in E. rhapontici, a pathogen
associated with crown rot in rhubarb, is accomplished through the
activity of a single enzyme, which has been located to the cell’s
periplasmic space (5).
This sucrose isomerase is strictly substrate specific toward sucrose,
with a Km of 0.28 M, whereby the reaction is essentially irreversible ).
The yield of palatinose formed from sucrose is about 85%. The
remaining 15% is trehalulose.
The most obvious characteristic of strains of Erwinia rhapontici
The pink pigmen is soluble in water and alcohol, but not in chloroform
Media which induce production of pink pigment : yeast-dextrose-
calcium carbonate agar, nutrient broth yeast extract agar, sucrosepeptone agar, nutrient glycerol and potato glucose agar, King’s B
medium, yeast-dextrose-chalk agar, and sucrose peptone agar, potato
glucose agar, and potato dextrose agar
Pink pigment of E. rhapontici was proferrorosamine A which chelates
iron, converting to ferrorosamine.
Proferrorosamine A is a metabolite of E. rhapontici.
Proferrorosamine A cause of iron deficiency in plants, and could also be
a virulence factor of E. rhapontici.
10 ppm : inhibited growth of wheat and cress seedlings.
100 ppm : strong inhibited germination of cress and wheat seeds
E. rhapontici can be isolated from water, soil, and plant surfaces.
E. rhapontici is an opportunistic bacterial plant pathogen and infects
its host trough wounds.
The other condition conducive to infection by E. rhapontici is a
prolonged period of high humidity.
E. rhapontici can overwinter on infected tissues of crops in western
Canada.
Strain of E. rhapontici are not host-specific.
Economic impact
• E. rhapontici can affect seed yield and seed quality.
• Field studies ofbpink seed of dry pea revealed that E. rhapontici
reduced the size, seedling emergence and pre-elongation seedling
height
• The seedling height was reduced by 46% compared to plants from
healthy seeds.
Seed treatment : phytobacteriomycin and dithane M-45
Biological control : Pseudomonas sp. And Bacillus subtilis.
The mechanism of action of antagonistic substances of B.subtilis
againts Erwinia spp. Was to damage the K+ ions transport of sensitive
phytopathogenic bacteria via cell walls.
Control of vectors : control of eelworm.