scholarly journals The combined use of Bacillus subtilis-based probiotic and anticoccidial herb had a better anti-Eimeria tenella efficiency

2021 ◽  
pp. 100181
Author(s):  
Yunqiao Yang ◽  
Fareed Uddin Memon ◽  
Kaiyuan Hao ◽  
Mingsheng Jiang ◽  
Lei Guo ◽  
...  
Keyword(s):  
Bacillus Subtilis ◽  
Eimeria Tenella ◽  
Combined Use

Synergistic effect of sequential or combined use of ozone and UV radiation for the disinfection of Bacillus subtilis spores

2008 ◽  
Vol 42 (6-7) ◽  
pp. 1613-1621 ◽  
Author(s):  
Yeon Jung Jung ◽  
Byung Soo Oh ◽  
Joon-Wun Kang
Keyword(s):  
Bacillus Subtilis ◽  
Synergistic Effect ◽  
Uv Radiation ◽  
Combined Use

scholarly journals The study of the antifungal activity of the Bacillus subtilis BZR 336g strain under the conditions of periodic cultivation with the addition of citric acid, corn extract and some microelements

2020 ◽  
Vol 21 ◽  
pp. 00015
Author(s):  
Anzhela Asaturova ◽  
Evgeny Gyrnets ◽  
Valeria Allakhverdian ◽  
Mikhail Astakhov ◽  
Ksenia Saenko
Keyword(s):  
Bacillus Subtilis ◽  
Citric Acid ◽  
Antifungal Activity ◽  
Liquid Culture ◽  
Complex Interaction ◽  
Crystalline Hydrate ◽  
Antifungal Metabolites ◽  
Qualitative And Quantitative ◽  
Test Culture ◽  
Combined Use

We studied the antifungal activity of the Bacillus subtilis BZR 336g strain against the test culture of the fungus Fusarium oxysporum var. orthoceras App. et Wr. BZR 6, depending on the addition of citric acid crystalline hydrate, a microelements solution and corn extract to the liquid nutrient medium. It was found that citric acid at a concentration of 15 g/l improves the bioavailability of microelements and increases antifungal activity. Corn extract and microelements without the formation of a chelate form with citric acid do not affect the fungicidal properties of B. subtilis BZR 336g. However, the corn extract at a concentration of 3 g / l increases the titer of bacteria in the liquid culture from 2 ± 0.1 × 108 to 1 ± 0.08 × 108 CFU/ml. The combined use of the studied components allowed us to achieve a significant increase in the antifungal activity of B. subtilis BZR 336g by 3.1 times. At the same time, the effect of synergism in their complex interaction was noted, which is probably due to a qualitative and quantitative change in the composition of B. subtilis BZR 336g antifungal metabolites.

STUDY OF THE BIOCOMPATIBILITY OF MUTANT STRAINS OF ROOT NODULE AND PGPR BACTERIA, PROMISING AS A BASIS OF MICROBIAL PREPARATIONS

2021 ◽  
Author(s):  
О.Н. ШЕМШУРА ◽  
Ж.Б. СУЛЕЙМЕНОВА ◽  
Ж.К. РАХМЕТОВА ◽  
Ж.Н. ШЕМШЕЕВА ◽  
Э.Т. ИСМАИЛОВА
Keyword(s):  
Bacillus Subtilis ◽  
Pseudomonas Putida ◽  
Mung Bean ◽  
Root Nodule ◽  
Nitrogen Fixing ◽  
Nodule Bacteria ◽  
Biological Product ◽  
Bean Plants ◽  
Combined Use ◽  
Mutant Strains

В статье приведены результаты исследования биосовместимости мутантных штаммов клубеньковых и PGPR бактерий (ризобактерий) с целью их совместного применения для культур маша и фасоли. По результатам проведенных исследований определены штаммы, проявившие контактную прогрессию и нейтралитет - Pseudomonas putidaМ-1 и Phyllobacterium sp. 35М; штаммы Bacillus subtilis М-2 и Chryseobacterium rhizoplanae 1М оказались наиболее перспективными в отношении совместного культивирования.Таким образом, подобраны консорциумы на основе мутантных штаммов азотфиксирующих и ростостимулирующих бактерий Pseudomonas putida М-1 и Chryseobacterium rhizoplanae для растений маша и Bacillus subtilis М-2 и Phyllobacterium sp. 35М - для растений фасоли. Полученные результаты открывают возможность комбинирования мутантных штаммов PGPR с ростостимулирующей активностью (Pseudomonas putida М-1, Bacillus subtilis М-2) и клубеньковыхбактерий (Phyllobacterium sp. 35М, Chryseobacterium rhizoplanae) с азотфиксирующей активностью с целью получения на их основе биопрепарата с сочетанными свойствами. The article presents the results of a study of the biocompatibility of mutant strains of nodule and PGPR bacteria with the aim of their combined use for mung bean and beans. According to the results of the studies, the strains that showed contact progression and neutrality were identified - Pseudomonas putida M-1 and Phyllobacterium sp. 35M; strains Bacillus subtilis M-2 and Chryseobacterium rhizoplanae 1M proved to be the most promising for co-cultivation. Thus, consortia were selected based on mutant strains of nitrogen-fixing and growth-stimulating bacteria Pseudomonas putida M-1 and Chryseobacterium rhizoplanae for mung bean and Bacillus subtilis M-2 and Phyllobacterium sp.35M for bean plants. The results obtained open up the possibility of combining mutant PGPR strains with growth-stimulating activity (Pseudomonas putida M-1, Bacillus subtilis M-2) and nodule bacteria with nitrogen-fixing activity (Phyllobacterium sp. 35M, Chryseobacterium rhizoplanae) in order to obtain a biological product with combined properties on their basis.

Integrated control of tobacco black shank by combined use of riboflavin and Bacillus subtilis strain Tpb55

BioControl ◽  
2017 ◽  
Vol 62 (6) ◽  
pp. 835-845 ◽  
Author(s):  
Chengsheng Zhang ◽  
Jiaming Gao ◽  
Teng Han ◽  
Xueying Tian ◽  
Fenglong Wang
Keyword(s):  
Bacillus Subtilis ◽  
Integrated Control ◽  
Subtilis Strain ◽  
Black Shank ◽  
Combined Use ◽  
Tobacco Black Shank

Protective immunity against Eimeria tenella infection in chickens following oral immunization with Bacillus subtilis expressing Eimeria tenella 3-1E protein

2015 ◽  
Vol 114 (9) ◽  
pp. 3229-3236 ◽  
Author(s):  
Zhiwei Lin ◽  
Yanyun Shi ◽  
Bin Deng ◽  
Xiangfei Mao ◽  
Dongyou Yu ◽  
...  
Keyword(s):  
Bacillus Subtilis ◽  
Protective Immunity ◽  
Oral Immunization ◽  
Eimeria Tenella

Use of Antibody to aid Visualization of Protein at the Termini of Bacteriophage Ø29 DNA

1980 ◽  
Vol 38 ◽  
pp. 540-541
Author(s):  
Dwight Anderson ◽  
Charlene Peterson ◽  
Gursaran Notani ◽  
Bernard Reilly
Keyword(s):  
Electron Microscopy ◽  
Bacillus Subtilis ◽  
Dna Synthesis ◽  
Restriction Endonuclease ◽  
Protein Complex ◽  
Protein Product ◽  
Viral Dna ◽  
Small Proteins ◽  
Antibody Labeling ◽  
Subtilis Bacteriophage

The protein product of cistron 3 of Bacillus subtilis bacteriophage Ø29 is essential for viral DNA synthesis and is covalently bound to the 5’-termini of the Ø29 DNA. When the DNA-protein complex is cleaved with a restriction endonuclease, the protein is bound to the two terminal fragments. The 28,000 dalton protein can be visualized by electron microscopy as a small dot and often is seen only when two ends are in apposition as in multimers or in glutaraldehyde-fixed aggregates. We sought to improve the visibility of these small proteins by use of antibody labeling.

Sign in / Sign up

Export Citation Format

Share Document