Bioconversion of Feather Composts using Proteolytic Bacillus mycoides for their Possible Application as Biofertilizer in Agriculture

Author(s):  
Goldy Primo Beryl ◽  
Basheer Thazeem ◽  
Mridul Umesh ◽  
Kandasamy Senthilkumar ◽  
Manickam Naveen Kumar ◽  
...  
Keyword(s):  
2021 ◽  
Vol 9 (1) ◽  
pp. 28-34
Author(s):  
Gallyndra Fatkhu Dinata ◽  
Nurul Ariani ◽  
Andik Purnomo ◽  
Luqman Qurata Aini

Penyakit busuk pangkal batang/moler (Fusarium oxysporum f.sp. cepae/FOC) merupakan salah satu faktor biotik dalam produksi bawang merah yang menyebabkan kerusakan hingga 50 %. Pengendalian biologi menawarkan strategi potensial pada perlindungan tanaman yang berfokus pada peran musuh alami dalam menekan hama dan penyakit tanaman. Penelitian ini bertujuan untuk mengidentifikasi dan mengetahui jenis bakteri yang berpotensi sebagai agens hayati terhadap penyakit moler pada bawang merah. Penelitian dilaksanakan di kondisi laboratorium dan lapang menggunakan rancangan acak kelompok untuk membandingkan setiap isolat dalam mengendalikan patogen. Sebanyak 5 dari 21 isolat bakteri menunjukkan sifat antagonisme yang tinggi terhadap FOC. Kelima isolat teridentifikasi sebagai Bacillus mycoides (K1), Clostridium sp. (K2), Pseudomonas sp. (K11), Erwinia sp. (K13), dan Pseudomonas sp. (K29). Pseudomonas sp menujukkan aktivitas penghambatan jamur sebesar 61,01 % dan 73,05 % di laboratorium, sedangkan Bacillus mycoides memberikan hasil terbaik pada kondisi lapang. K2 dan K29 menunjukkan hasil terbaik dalam meningkatkan tinggi tanaman dibandingkan dengan kontrol. Sementara itu, K29 juga berpotensi meningkatkan jumlah daun dan berat basah tanaman.


2021 ◽  
Vol 36 ◽  
pp. 05003
Author(s):  
Nguyen Van Zhang ◽  
Nguyen Thi Thu ◽  
Vu Thi Linh ◽  
V.V. Pylnev ◽  
M.I. Popchenko

This work presents the experimental study results of the influence of the culture medium on the ability to IAA synthesis of three endophytic strains TH10R, TH11T, and TH13T from roots of Ipomoea pes-caprae. Three investigated strains give the highest IAA concentration after 96 h of cultivation. A significant increase in IAA biosynthesis was obtained by cultivating the TH10R strain in a medium containing lactose or starch as a carbon source and NH4Cl or KNO3 as a nitrogen source. The TH11T strain produces the maximum amount of IAA, using glucose or xylose and KNO3 or NH4NO3 as carbon and nitrogen sources, respectively. Sucrose is a suitable carbon source for the TH13T strain; on a sucrose-containing medium, the TH13T strain produces the highest IAA amount. The most active strain is TH10R, identified as Bacillus mycoides and named Bacillus mycoides TH10R.


2020 ◽  
Vol 70 (1) ◽  
Author(s):  
Elisa Steiner ◽  
Rosa Margesin

Abstract Purpose To evaluate the production of a cold-active CMCase (endoglucanase) by Bacillus mycoides AR20-61 isolated from Alpine forest soil and to characterize the crude enzyme. Methods After studying the effect of cultivation parameters (medium composition, temperature, NaCl concentration, pH) on bacterial growth and enzyme production, the crude enzyme was characterized with regard to the effect of pH, temperature, and inhibitors on enzyme activity and stability. Result Optimum growth and enzyme production occurred at 20–25 °C, pH 7, and 1–1.5% (w/v) CMC. Despite high biomass production over the whole growth temperature range (10–35 °C), enzyme production was low at 10 and 35 °C. CMC concentration had a minor effect on growth, independent of the growth temperature, but a significant effect on CMCase production at temperatures ≥ 20 °C. The crude enzyme was active over a broad temperature range (0–60 °C); the apparent optimum temperature for activity was at 40–50 °C. The cultivation temperature influenced the effect of temperature on enzyme activity and stability. A significantly higher thermosensitivity of the enzyme produced at a cultivation temperature of 10 °C compared to that produced at 25 °C was noted at 50 and 65 °C. The enzyme was highly active over a pH range of 4–6 and showed optimum activity at pH 5. No activity was lost after 60 min of incubation at 30 °C and pH 4–9. The CMCase was resistant against a number of monovalent and divalent metal ions, metal-chelating agents, and phenol. Conclusion The CMCase produced by the studied strain is characterized by high activities in the low temperature range (down to 0 °C) and acidic pH range, high stability over a broad pH range, and high resistance against a number of effectors. Our results also demonstrate the different, independent roles of temperature in bacterial growth, enzyme production, nutrient requirements during enzyme production, and enzyme characteristics regarding thermosensitivity, which has not yet been described for cellulases.


1984 ◽  
Vol 30 (5) ◽  
pp. 691-698 ◽  
Author(s):  
Anna S. Tikhonenko ◽  
Nina N. Belyaeva ◽  
Anna F. Kretova

The relationship between large and small particles of phages No. 1M and H17 reproducing simultaneously in one and the same bacterial cell of Bacillus mycoides was studied by the immune electron microscopic technique. The large particles of phages No. 1M and H17 were morphologically identical with phage No. 1 of B. mycoides, whereas only the tails of small particles of phages No. 1M and H17 were morphologically identical with the tail of phage No. 1. Antigens were identified in phages No. 1, No. 1M, and H17 using specific antibodies against phage No. 1, containing only large phage particles, and specific antibodies against phage H17 small heads. It was shown that (i) all structural elements of large particles and tails of small particles of phage No. 1M were antigenically identical with those of phage No. 1; (ii) all structural elements of small and large particles of phage H17, except the inner core of the tail, were antigenically different from phage No. 1; and (iii) the small heads of phages No. 1M and H17 were antigenically identical. Particles of phage No. 1 are morphologically and antigenically identical with the large particles of phage No. 1M and are antigenically different from the large particles of phage H17. Since the tails of small and large particles are antigenically identical in each phage pair (No. 1M and H17), this suggests that in both cases, the genome of a small defective phage codes for the synthesis of head proteins only, whereas its tail is borrowed from the corresponding helper phage. The small phage may therefore be considered as a satellite of the large phage which depends on a helper partner for production of complete particles and whose tail proteins are identical with those of the helper phage.


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