Facilitated enumeration of the silicate bacterium Paenibacillus mucilaginosus comb. nov. (formerly Bacillus mucilaginosus) via tetrazolium chloride incorporation into a double agar-based solid growth medium

2017 ◽  
Vol 63 (3) ◽  
pp. 401-404
Author(s):  
Annie Vardanian ◽  
Eyal Kurzbaum ◽  
Yair Farber ◽  
Monica Butnariu ◽  
Robert Armon
Keyword(s):  
Growth Medium ◽  
Bacillus Mucilaginosus ◽  
Tetrazolium Chloride ◽  
Paenibacillus Mucilaginosus ◽  
Silicate Bacterium

scholarly journals Transfer of Bacillus mucilaginosus and Bacillus edaphicus to the genus Paenibacillus as Paenibacillus mucilaginosus comb. nov. and Paenibacillus edaphicus comb. nov.

2010 ◽  
Vol 60 (1) ◽  
pp. 8-14 ◽  
Author(s):  
Xiu-Fang Hu ◽  
Shi-Xiao Li ◽  
Jin-Guang Wu ◽  
Jian-Feng Wang ◽  
Qiong-Lou Fang ◽  
...  
Keyword(s):  
Fatty Acid ◽  
16S Rrna ◽  
Dna Hybridization ◽  
Type Strain ◽  
Sequence Similarity ◽  
Methyl Esters ◽  
Diaminopimelic Acid ◽  
Gene Sequences ◽  
Bacillus Mucilaginosus ◽  
Paenibacillus Mucilaginosus

Bacillus mucilaginosus and Bacillus edaphicus were reclassified based on their 16S rRNA and gyrB gene sequences, DNA–DNA hybridization, fatty acid methyl esters and other taxonomic characteristics. Phylogenetic analysis based on 16S rRNA and gyrB gene sequences indicated that strains of B. mucilaginosus and B. edaphicus were members of the genus Paenibacillus, with over 90.4 % and 70.3 % sequence similarity, respectively. Their DNA G+C contents were 54.5–56.8 mol%. The DNA–DNA relatedness values of B. edaphicus VKPM B-7517T with B. mucilaginosus KNP414 and B. mucilaginosus CGMCC 1.236 were 89.2 % and 88.7 %, respectively. The major isoprenoid quinone of B. mucilaginosus and B. edaphicus was MK-7 (94.1–95.7 %). The peptidoglycan type was A1γ (meso-diaminopimelic acid) and the major polar lipids were phosphatidylglycerol and diphosphatidylglycerol. The major fatty acids were anteiso-C15 : 0, C16 : 1 ω11c and C16 : 0. Phenotypic features and fatty acid profiles supported the similarity of B. mucilaginosus and B. edaphicus to Paenibacillus validus CCTCC 95016T and confirmed their relationship with members of the genus Paenibacillus. Therefore, it is proposed that Bacillus mucilaginosus and Bacillus edaphicus be transferred to the genus Paenibacillus as Paenibacillus mucilaginosus comb. nov. (type strain HSCC 1605T=VKPM B-7519T=VKM B-1480DT=CIP 105815T=KCTC 3870T) and Paenibacillus edaphicus comb. nov. (type strain VKPM B-7517T=DSM 12974T=CIP 105814T), respectively.

Ultrastructural Alterations in Hela Cells Induced by Spider Venom

1967 ◽  
Vol 25 ◽  
pp. 20-21
Author(s):  
Dale E. McClendon ◽  
Paul N. Morgan ◽  
Bernard L. Soloff
Keyword(s):  
Growth Medium ◽  
Mammalian Cells ◽  
Carcinoma Cells ◽  
Venom Protein ◽  
Sterile Saline ◽  
Carbon Coated ◽  
Available Information ◽  
Loxosceles Reclusa ◽  
Essential Growth ◽  
Solution Cultures

It has been observed that minute amounts of venom from the brown recluse spider, Loxosceles reclusa, are capable of producing cytotoxic changes in cultures of certain mammalian cells (Morgan and Felton, 1965). Since there is little available information concerning the effect of venoms on susceptible cells, we have attempted to characterize, at the electron microscope level, the cytotoxic changes produced by the venom of this spider.Cultures of human epithelial carcinoma cells, strain HeLa, were initiated on sterile, carbon coated coverslips contained in Leighton tubes. Each culture was seeded with approximately 1x105 cells contained in 1.5 ml of a modified Eagle's minimum essential growth medium prepared in Hank's balanced salt solution. Cultures were incubated at 36° C. for three days prior to the addition of venom. The venom was collected from female brown recluse spiders and diluted in sterile saline. Protein determinations on the venom-were made according to the spectrophotometric method of Waddell (1956). Approximately 10 μg venom protein per ml of fresh medium was added to each culture after discarding the old growth medium. Control cultures were treated similarly, except that no venom was added. All cultures were reincubated at 36° C.

Effect of Iron Limitation on the Ultrastructure of Agmenellum Quadruplicatum

1981 ◽  
Vol 39 ◽  
pp. 410-411
Author(s):  
L. P. Hardie ◽  
D. L. Balkwill ◽  
S. E. Stevens
Keyword(s):  
Growth Medium ◽  
Green Alga ◽  
Natural Habitat ◽  
Iron Limitation ◽  
Natural Environments ◽  
Blue Green Alga ◽  
Marine Cyanobacterium ◽  
Natural Systems ◽  
Thin Sectioning ◽  
Agmenellum Quadruplicatum

Agmenellum quadruplicatum is a unicellular, non-nitrogen-fixing, marine cyanobacterium (blue-green alga). The ultrastructure of this organism, when grown in the laboratory with all necessary nutrients, has been characterized thoroughly. In contrast, little is known of its ultrastructure in the specific nutrient-limiting conditions typical of its natural habitat. Iron is one of the nutrients likely to limit this organism in such natural environments. It is also of great importance metabolically, being required for both photosynthesis and assimilation of nitrate. The purpose of this study was to assess the effects (if any) of iron limitation on the ultrastructure of A. quadruplicatum. It was part of a broader endeavor to elucidate the ultrastructure of cyanobacteria in natural systemsActively growing cells were placed in a growth medium containing 1% of its usual iron. The cultures were then sampled periodically for 10 days and prepared for thin sectioning TEM to assess the effects of iron limitation.

Cultivation and Harvesting of Selenium-Enriched Ganoderma lingzhi and Spent Medium Using Kudzu Vine as Substrate

2019 ◽  
Vol 18 (2) ◽  
pp. 152-157
Author(s):  
Zeng Xianlu ◽  
Han Fei ◽  
Zhong Yanmei
Keyword(s):  
Growth Medium ◽  
Wheat Bran ◽  
Fruiting Body ◽  
Sodium Selenite ◽  
Human Consumption ◽  
Growth Substrate ◽  
Organic Selenium ◽  
Significant Difference ◽  
Ganoderma Lingzhi ◽  
Run Speed

In order to harvest selenium-enriched fruiting body and spores of Ganoderma lingzhi and spent medium, G. lingzhi was cultivated in kudzu vine as substrate and the bio-transformation of selenite was evaluated. The growth medium consisted of Kudzu vine supplemented with 20% wheat bran or sawdust or none. The growth medium was supplemented with 0, 10, 20, 30, and 50 mg/kg of sodium selenite. We found a significant difference in spawn run speed, fruiting body and spore yields when Kudzu vine was supplemented with wheat bran or sawdust. However, when whole-kudzu vine was used alone as substrate, it resulted in a significantly lower spawn run speed, fruiting body, and spore yields compared with kudzu vine + sawdust substrate and kudzu vine + wheat bran substrate. The selenium content in fruiting body and spores increased with increasing sodium selenite supplementation and approximately equaled half of the selenium in the substrate. No selenite was detected in both the fruiting body and spores. However, in the spent medium when sodium selenite was supplemented at 10, 20, 30, 50 mg/kg, the residual selenite concentration decreased to 0.45, 0.72, 1.29, and 1.95 mg/kg, respectively, suggesting a higher selenite transformation (92.27–93.57%). In conclusion, if Ganoderma fruiting body and spores were to be harvested for human consumption, approximately 50 mg/kg selenite should be added to the growth substrate. On the other hand, if the spent medium was to be used as an organic selenium source, the optimal sodium selenite supplementation level would be 10 mg/kg.

Selenium Uptake by a Coal Mine Wetland Sediment

2003 ◽  
Vol 38 (3) ◽  
pp. 483-497 ◽  
Author(s):  
Susan A. Baldwin ◽  
Al Henry Hodaly
Keyword(s):  
Growth Medium ◽  
Coal Mine ◽  
Mine Waste ◽  
Reduction Rate ◽  
Plant Debris ◽  
Bacteria Growth ◽  
Sulfate Reducing ◽  
Selenium Uptake ◽  
Negative Effect ◽  
Reducing Bacteria

Abstract Sediment from a wetland receiving runoff from a coal mine waste dump in the Elk River Valley of southeast British Columbia was assessed for potential selenium uptake. Selenite [SeO32-, Se(IV)] was found to adsorb to the washed sediment at pH 7 to 8, whereas no selenate [SeO42-, Se(VI)] was adsorbed, in the concentration range of 8 to 225 μg L-1 Se as selenite or selenate. Sulfate- and selenate-reducing bacterial activity was detected in the sediment. In the presence of sulfate-reducing bacteria growth medium, Se as selenate was reduced from 619(±53) μg L-1 to 15(±0.7) μg L-1, and in the presence of selenate-reducing bacteria growth medium, Se as selenate was reduced from 364(±66) mg L-1 to 22(±10) mg L-1. Semi-continuous microcosms containing sediment overlaid with selenate (500 μg L-1 Se) and sulfate (0.9 g L-1) containing water were amended with plant debris from the site or nutrients (lactate and fertilizer). Potential selenate reduction rate (0.76 h-1) was highest in the unamended microcosms. Amendment with plant debris from the site had a negative effect on selenate reduction rate in the short term (after one hour) and a positive effect on Se removal in the long term (after one week). This study suggests that wetland sediments at the mine site may be important sinks for Se.

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