Biotin Detected by Agar Plate Bioassay in Purified Soybean Protein

2016 ◽  
Vol 10 (1) ◽  
pp. 263-268
Author(s):  
Makoto Muratsugu ◽  
Chihiro Tsunoya ◽  
Manami Furuhata ◽  
Kiyomi Ogata ◽  
Tomoko Akashi ◽  
...  
2017 ◽  
Vol 3 (1) ◽  
pp. 1 ◽  
Author(s):  
Makoto Muratsugu ◽  
Kaori Washino ◽  
Yoshiko Onchi ◽  
Akane Yamaguchi ◽  
Ayano Kumaki ◽  
...  

<p><span style="font-family: Times New Roman;"><span style="font-size: medium;">The change of biotin level during production of natto (Japanese fermented soybean) was investigated in this study.  </span><span style="font-size: medium;">The total biotin level was measured by an agar plate bioassay using </span><em><span style="font-size: medium;">Lactobacillus plantarum</span></em><span style="font-size: medium;"> ATCC 8014.</span><span style="font-size: medium;">  </span><span style="font-size: medium;">The total biotin level decreased during water soaking, but increased after the fermentation of soybeans using </span><em><span style="font-size: medium;">Bacillus subtilis</span></em><span style="font-size: medium;"> var. </span><em><span style="font-size: medium;">natto</span></em><span style="font-size: medium;"> (</span><em><span style="font-size: medium;">B. natto</span></em><span style="font-size: medium;">) and reached a maximum level.</span><span style="font-size: medium;">  </span><span style="font-size: medium;">The increase of total biotin was not affected by Asp, Arg, and Ile which promoted the growth of </span><em><span style="font-size: medium;">L. plantarum</span></em><span style="font-size: medium;"> in high concentrations. </span><span style="font-size: medium;"> </span><span style="font-size: medium;">The peak level of biotin in the fermented soybeans was significantly higher than that of dry soybeans.</span><span style="font-size: medium;">  </span><span style="font-size: medium;">The fermented soybeans at the biotin peak level were adequate for food.</span><span style="font-size: medium;">  </span><span style="font-size: medium;">In addition, we detected 9 and 4 biotinylated polypeptides in the soybeans and </span><em><span style="font-size: medium;">B. natto</span></em><span style="font-size: medium;"> used in this study, respectively.</span><span style="font-size: medium;">  </span><span style="font-size: medium;">We speculated that the increase of biotin level may depend on the increase of the 4 biotinylated polypeptides and free biotin in </span><em><span style="font-size: medium;">B. natto</span></em><span style="font-size: medium;">.</span></span></p>


2004 ◽  
Vol 94 (11) ◽  
pp. 1228-1234 ◽  
Author(s):  
L. Meadow Anderson ◽  
Virginia O. Stockwell ◽  
Joyce E. Loper

Pseudomonas fluorescens A506 and Pantoea agglomerans strains Eh252 and C9-1 are biological control agents that suppress fire blight, an important disease of pear and apple caused by the bacterium Erwinia amylovora. Pseudomonas fluorescens strain A506 suppresses disease largely through competitive exclusion of E. amylovora on surfaces of blossoms, the primary infection court, whereas Pantoea agglomerans strains Eh252 and C9-1 produce antibiotics that are toxic to E. amylovora. In this study, an extracellular protease produced by A506 is characterized and evaluated for its capacity to inactivate the antibiotics produced by the strains of Pantoea agglomerans. Activity of the extracellular protease was optimal at pH 9 and inhibited by zinc- or calcium-chelators, indicating that the protease is an alkaline metalloprotease. In an agar plate bioassay, partially purified extracellular protease inactivated the antibiotics mccEh252 and herbicolin O, which are produced by Pantoea agglomerans strains Eh252 and C9-1, respectively. Derivatives of A506 deficient in extracellular protease production were obtained by transposon mutagenesis, and the aprX gene encoding the protease was cloned and sequenced. Strain A506 inactivated mccEh252 and herbicolin O in agar plate bioassays, whereas the aprX mutant did not inactivate the antibiotics. Both A506 and the aprX mutant were insensitive to antibiosis by C9-1 and Eh252; thus, the protease was not required to protect A506 from antibiosis. These data highlight a previously unknown role of the extracellular protease produced by Pseudomonas fluorescens A506 in interactions among plant-associated microbes.


1968 ◽  
Vol 27 (2) ◽  
pp. 484 ◽  
Author(s):  
A. J. Clifford ◽  
A. D. Tillman
Keyword(s):  

2019 ◽  
Author(s):  
Jordan B Gregg

AIEC-LF82 is a strain of bacteria that is surmised to have a role in causing IBD and Crohn’s disease by activating pro-inflammatory gene expression in organisms. Using antibiotics via combination therapy has been a technique used in clinical settings in an attempt to treat the strains, however, the attempts have not been that effective nor efficient in terms of completely halting the growth and colonization of AIEC to treat IBD and Crohn's disease patients. Research has shown that regarding hindering or preventing the colonization bacterial colonies, sequential therapy tends to be more effective and time-efficient than combination therapy, with fewer adverse effects. To test if this is also the case with the AIEC-LF82 strain of bacteria, I first tested AIEC’s response to combination therapy using the Penicillin-Streptomycin, Kanamycin-Chloramphenicol, antimicrobial peptide (AMP), Kanamycin, SPE phase and LB agar plates, all of which were experimental plates other than the LB agar plate that acted as the negative control. I then tested AIEC-LF82’s response to sequential therapy using the LB+ Kan + Spe, LB + AMP + Spe, LB+ Kan/Cam + Spe, LB + P/S + Spe, LB + P/S + Kan and LB + P/S + AMP and one LB agar plate acting as the negative control. The only differences between sets a and b were the order in which antibiotics were administered in the six aforementioned treatment sets. Ultimately, I found that set b of sequential therapy, strong-weak antibiotic treatments, was the most effective treatment but that set a regarding sequential therapy was actually the least effective of all of the treatments. In conclusion, using strong-weak sequential antibiotic therapy treatments appears to be a potentially promising option to treat patients suffering from Crohn's disease and IBD.


1969 ◽  
Vol 61 (4) ◽  
pp. 601-603 ◽  
Author(s):  
T. Hymowitz ◽  
F. I. Collins ◽  
S. J. Gibbons
Keyword(s):  

1969 ◽  
Vol 16 (1) ◽  
pp. 10-14 ◽  
Author(s):  
KAZUMOTO HASHIZUME ◽  
SHINICHIRO KITA ◽  
TOKUJI WATANABE
Keyword(s):  

Author(s):  
Junping Yu ◽  
Guolong Zhao ◽  
Wei Li ◽  
Ying Zhang ◽  
Peng Wang ◽  
...  

Abstract Key message Identification and functional analysis of the male sterile gene MS6 in Glycine max. Abstract Soybean (Glycine max (L.) Merr.) is an important crop providing vegetable oil and protein. The male sterility-based hybrid breeding is a promising method for improving soybean yield to meet the globally growing demand. In this research, we identified a soybean genic male sterile locus, MS6, by combining the bulked segregant analysis sequencing method and the map-based cloning technology. MS6, highly expressed in anther, encodes an R2R3 MYB transcription factor (GmTDF1-1) that is homologous to Tapetal Development and Function 1, a key factor for anther development in Arabidopsis and rice. In male sterile ms6 (Ames1), the mutant allele contains a missense mutation, leading to the 76th leucine substituted by histidine in the DNA binding domain of GmTDF1-1. The expression of soybean MS6 under the control of the AtTDF1 promoter could rescue the male sterility of attdf1 but ms6 could not. Additionally, ms6 overexpression in wild-type Arabidopsis did not affect anther development. These results evidence that GmTDF1-1 is a functional TDF1 homolog and L76H disrupts its function. Notably, GmTDF1-1 shows 92% sequence identity with another soybean protein termed as GmTDF1-2, whose active expression also restored the fertility of attdf1. However, GmTDF1-2 is constitutively expressed at a very low level in soybean, and therefore, not able to compensate for the MS6 deficiency. Analysis of the TDF1-involved anther development regulatory pathway showed that expressions of the genes downstream of TDF1 are significantly suppressed in ms6, unveiling that GmTDF1-1 is a core transcription factor regulating soybean anther development.


2020 ◽  
Vol 58 (10) ◽  
pp. 1759-1767
Author(s):  
Mieke Steenbeke ◽  
Sander De Bruyne ◽  
Jerina Boelens ◽  
Matthijs Oyaert ◽  
Griet Glorieux ◽  
...  

AbstractObjectivesIn this study, the possibilities of Fourier-transformed infrared spectroscopy (FTIR) for analysis of urine sediments and for detection of bacteria causing urinary tract infections (UTIs) were investigated.MethodsDried urine specimens of control subjects and patients presenting with various nephrological and urological conditions were analysed using mid-infrared spectroscopy (4,000–400 cm−1). Urine samples from patients with a UTI were inoculated on a blood agar plate. After drying of the pure bacterial colonies, FTIR was applied and compared with the results obtained by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Chemometric data analysis was used to classify the different species.ResultsDue to the typical molecular assignments of lipids, proteins, nucleic acids and carbohydrates, FTIR was able to identify bacteria and showed promising results in the detection of proteins, lipids, white and red blood cells, as well as in the identification of crystals. Principal component analysis (PCA) allowed to differentiate between Gram-negative and Gram-positive species and soft independent modelling of class analogy (SIMCA) revealed promising classification ratios between the different pathogens.ConclusionsFTIR can be considered as a supplementary method for urine sediment examination and for detection of pathogenic bacteria in UTI.


Parasitology ◽  
2019 ◽  
Vol 146 (12) ◽  
pp. 1602-1614 ◽  
Author(s):  
Hesham M. Al-Mekhlafi ◽  
Nabil A. Nasr ◽  
Yvonne A. L. Lim ◽  
Fatin Nur Elyana ◽  
Hany Sady ◽  
...  

AbstractThis cross-sectional study aimed to determine the prevalence and risk factors of S. stercoralis infection among 1142 Orang Asli primary schoolchildren in six different states of Peninsular Malaysia. Fecal samples were examined using direct smear, formalin-ether sedimentation (FES), agar plate culture (APC) and PCR techniques. Overall, 15.8% of the children were found to be infected with S. stercoralis. The prevalence was 0.2, 1.3, 15.2 and 13.7% by direct smear, FES, APC and PCR, respectively. Multivariate analysis showed that an age of >10 years, being male, belonging to a Proto-Malay tribe, belonging to the Senoi tribe, indiscriminate defecation, using an unimproved water source for drinking water and not wearing shoes when outside were the significant risk factors of infection among these children. In conclusion, we provide new evidence on the occurrence of S. stercoralis in Malaysia to show that there is a relatively high prevalence of infection among Orang Asli schoolchildren. Therefore, the use of specific methods for detecting S. stercoralis should be considered when screening these children for intestinal parasites. Moreover, prevention and control measures specific to S. stercoralis should be integrated into the intestinal parasitic infections control programme in Malaysia.


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