Immunological detection of the GerA spore germination proteins in the spore integuments of Bacillus subtilis using scanning electron microscopy

1996 ◽  
Vol 139 (2-3) ◽  
pp. 235-238
Author(s):  
Y YASUDA ◽  
Y SAKAE ◽  
K TOCHIKUBO
1990 ◽  
Vol 68 (10) ◽  
pp. 2054-2058 ◽  
Author(s):  
Béatrice Mathéron ◽  
Abdellatif Benbadis

Date palm seedlings were inoculated at the two-leaf stage with Fusarium oxysporum f. sp. albedinis, the causal agent of Bayoud. Following spore germination, hyphae bore a bole through the walls of the root epidermis and penetrated into the cortical parenchyma. The fungus then grows inter- or intra-cellularly towards the central cylinder and enters the xylem vessels. There, it continues to grow towards the leaves. The progression from vessel to vessel is achieved through bordered pits. The cultivar Deglet-Nour, known for its susceptibility to this wilt disease, exhibited no early reaction to the presence of the parasite in its tissues. Key words: date palm, Fusarium oxysporum f. sp. albedinis, scanning electron microscopy.


2016 ◽  
Vol 82 (2) ◽  
Author(s):  
Irma KRESNAWATY ◽  
Agustin Sri MULYATNI ◽  
Deden Dewantara ERIS ◽  
Haryo Tejo PRAKOSO

AbstractThe difficulties in processing of petroleum-based plastic waste had encouraged the development of biodegradable plastics polyhydroxyalkanoate (PHA). Researchers isolated the PHA-producing microorganisms from various sources to obtain new species with high PHA production capability. In addition, the high cost of PHA production might be overcome by using carbon-rich waste, such as palm oil mill effluent (POME). This research conducted characterization of produced PHA and optimization of PHA production in POME. In previous research, three potential isolates were obtained, which are one Pseudomonas aeruginosa isolate and two Bacillus subtilis isolates. Analysis of Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) showed the presence of PHA accumu-lation within the bacterial cell. The results of Spectra of Fourier Transform Infra Red Spectroscopy (FT-IR) revealed differences in C-C and C-H alipathic regions of PHA produced by Pseudomonas aeruginosa and Bacillus subtilis. Optimum production of PHA was obtained using POME at concentration of 50-25% during 6 days of incubation time in an enriched media pretreatment.Abstrak Sulitnya pengolahan limbah plastik berbasis minyak bumi mendorong pengembangan plastik biodegradable poli-hidroksialkanoat (PHA). Beberapa peneliti mengisolasi mikroorganisme penghasil  PHA dari berbagai sumber karena diharapkan akan diperoleh spesies baru dengan kemampuan produksi PHA yang tinggi. Selain itu kendala tingginya biaya produksi PHA dapat diatasi dengan peman-faatan limbah yang kaya akan  karbon, seperti limbah cair pabrik kelapa sawit (LCPKS). Pada penelitian ini dilakukan karakterisasi PHA yang dihasilkan dan optimasi produksi PHA pada LCPKS. Pada penelitian sebelumnya telah diperoleh  tiga isolat potensial, yaitu : satu isolat  Pseudo-monas aeruginosa dan dua isolat  Bacillus subtilis.  Analisis Scanning Electron Microscopy (SEM) dan Transmission Electon Microscopy (TEM) menunjukkan adanya akumulasi PHA di dalam sel bakteri. Dari hasil analisis FT-IR disimpulkan bahwa senyawa PHA yang dihasilkan Pseudo-monas aeruginosa  berbeda dengan  Bacillus subtilisyang ditandai   perbedaan   pada  spectra   gugus  C-C  dan   C-H alifatik.  Produksi optimum PHA diperoleh pada konsentrasi LCPKS 50-25%, waktu inkubasi  enam hari dan optima-lisasi pertumbuhan pada media kaya di awal untuk mening-katkan populasi mikroba.


2016 ◽  
Vol 82 (2) ◽  
Author(s):  
Irma KRESNAWATY ◽  
Agustin Sri MULYATNI ◽  
Deden Dewantara ERIS ◽  
Haryo Tejo PRAKOSO

AbstractThe difficulties in processing of petroleum-based plastic waste had encouraged the development of biodegradable plastics polyhydroxyalkanoate (PHA). Researchers isolated the PHA-producing microorganisms from various sources to obtain new species with high PHA production capability. In addition, the high cost of PHA production might be overcome by using carbon-rich waste, such as palm oil mill effluent (POME). This research conducted characterization of produced PHA and optimization of PHA production in POME. In previous research, three potential isolates were obtained, which are one Pseudomonas aeruginosa isolate and two Bacillus subtilis isolates. Analysis of Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) showed the presence of PHA accumu-lation within the bacterial cell. The results of Spectra of Fourier Transform Infra Red Spectroscopy (FT-IR) revealed differences in C-C and C-H alipathic regions of PHA produced by Pseudomonas aeruginosa and Bacillus subtilis. Optimum production of PHA was obtained using POME at concentration of 50-25% during 6 days of incubation time in an enriched media pretreatment.Abstrak Sulitnya pengolahan limbah plastik berbasis minyak bumi mendorong pengembangan plastik biodegradable poli-hidroksialkanoat (PHA). Beberapa peneliti mengisolasi mikroorganisme penghasil  PHA dari berbagai sumber karena diharapkan akan diperoleh spesies baru dengan kemampuan produksi PHA yang tinggi. Selain itu kendala tingginya biaya produksi PHA dapat diatasi dengan peman-faatan limbah yang kaya akan  karbon, seperti limbah cair pabrik kelapa sawit (LCPKS). Pada penelitian ini dilakukan karakterisasi PHA yang dihasilkan dan optimasi produksi PHA pada LCPKS. Pada penelitian sebelumnya telah diperoleh  tiga isolat potensial, yaitu : satu isolat  Pseudo-monas aeruginosa dan dua isolat  Bacillus subtilis.  Analisis Scanning Electron Microscopy (SEM) dan Transmission Electon Microscopy (TEM) menunjukkan adanya akumulasi PHA di dalam sel bakteri. Dari hasil analisis FT-IR disimpulkan bahwa senyawa PHA yang dihasilkan Pseudo-monas aeruginosa  berbeda dengan  Bacillus subtilisyang ditandai   perbedaan   pada  spectra   gugus  C-C  dan   C-H alifatik.  Produksi optimum PHA diperoleh pada konsentrasi LCPKS 50-25%, waktu inkubasi  enam hari dan optima-lisasi pertumbuhan pada media kaya di awal untuk mening-katkan populasi mikroba.


1972 ◽  
Vol 112 (3) ◽  
pp. 1383-1386 ◽  
Author(s):  
R. P. George ◽  
R. M. Albrecht ◽  
K. B. Raper ◽  
I. B. Sachs ◽  
A. P. MacKenzie

1990 ◽  
Vol 68 (9) ◽  
pp. 1953-1961 ◽  
Author(s):  
H. Lehnackers ◽  
W. Knogge

Seven races of Rhynchosporium secalis were screened for their virulence on a variety of barley cultivars. Four races were identified as virulent on cultivar Atlas 46 (resistance loci Rrs1 and Rrs2) but virulent on the near-isogenic cultivar Atlas (Rrs2). For one of these races, US238.1, the fungal infection cycle was followed on the susceptible cultivar by means of light and scanning electron microscopy. From a comparative analysis of fungal development on the susceptible and resistant cultivars, two lines of plant defense emerged: (i) inhibition of spore germination on the leaf surface and (ii) prevention of the establishment of the subcuticular stroma. Investigations of the development of race US238.1 on different barley cultivars with and without Rrs1 and on F1 individuals from different crosses excluded involvement of Rrs1 in the inhibition of spore germination. Possible pathogenicity mechanisms are discussed. Key words: leaf scald, microscopy, plant resistance.


1999 ◽  
Vol 62 (4) ◽  
pp. 368-379 ◽  
Author(s):  
D. LINDSAY ◽  
A. von HOLY

Three commercial sanitizers containing iodophor (I), peracetic acid/hydrogen peroxide (PAH), or chlorhexidine gluconate (CG) were evaluated in vitro against planktonic and sessile Bacillus subtilis or Pseudomonas fluorescens cells grown in Standard One Nutrient Broth. Sessile cells were attached to stainless steel or polyurethane test surfaces. Planktonic and attached cells of both bacteria were enumerated by plate counts after sanitizer treatment for 1, 3, or 5 min. Sessile cells were dislodged from test surfaces by shaking them with beads. Cell morphologies were monitored by scanning electron microscopy (SEM). Attached B. subtilis and P. fluorescens cells on both surface types were less susceptible to all three sanitizers than their planktonic counterparts. PAH, I, and CG were equally effective against planktonic P. fluorescens cells, which were reduced by 99.999% after 1, 3, and 5 min exposure. PAH was the only sanitizer effective against attached P. fluorescens cells on both surface types; it reduced counts by ≤99.9% after 1, 3, and 5 min exposure. PAH was also the most effective sanitizer against planktonic B. subtilis cells, reducing counts by 99.9% after 1, 3, and 5 min. Sessile B. subtilis cells on both surface types were the least susceptible to all sanitizers; counts were reduced by only 99.5% or less after exposure to PAH for 5 min. SEM revealed that planktonic and attached cells of both bacteria exhibited symptoms of surface roughness, indentations, and shape distortions after treatment with any of the sanitizers.


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