Morphological Characterization of Rhinacanthus Species of Sri Lanka

Planta Medica ◽  
2010 ◽  
Vol 76 (05) ◽  
Author(s):  
APPR Amarasinghe ◽  
RP Karunagoda ◽  
DSA Wijesundara
Phytotaxa ◽  
2021 ◽  
Vol 513 (3) ◽  
pp. 265-270
Author(s):  
DUILIO IAMONICO ◽  
SINDHU ARYA ◽  
VENUGOPALAN NAIR SARADAMMA ANIL KUMAR

Indobanalia thyrsiflora is an endemic species occurring in peninsular India (Andhra Pradesh, Karnataka, Kerala and Tamil Nadu States) and Sri Lanka. A nomenclatural study of the basionym Banalia thyrsiflora, published by Moquin-Tandon in Candolle’s Prodromus (year 1849), is carried out and the name is lectotypified on a specimen deposited at P (barcode P00609924); isolectotypes are traced at K and CAL. A preliminary morphological characterization of the species is also given, based on field surveys and examination of herbarium specimens. We noted that I. thyrsiflora is highly variable. However, we prefer to avoid, for the moment, taxonomic conclusions about the various morphotypes found, waiting the complete results of this ongoing morphological and molecular investigations.


2018 ◽  
Vol 29 (2) ◽  
pp. 167
Author(s):  
W. M. R. Kumari ◽  
D. K. N. G. Pushpakumara ◽  
W. M. W. Weerakoon ◽  
D. M. J. B. Senanayake ◽  
H. D. Upadhyaya

2015 ◽  
Vol 24 (4) ◽  
pp. 362 ◽  
Author(s):  
S.M.P.C. Padmini ◽  
D.K.N.G. Pushpakumara ◽  
R. Samarasekera

2018 ◽  
Vol 113 (2) ◽  
pp. 96-105
Author(s):  
H.P.T. Sasanka HEWATHILAKE ◽  
N.W.B. BALASOORIYA ◽  
Yoshihiro NAKAMURA ◽  
H.M.T.G.A. PITAWALA ◽  
H.W.M. Athula Chandana WIJAYASINGHE ◽  
...  

2015 ◽  
Vol 25 (1) ◽  
pp. 127
Author(s):  
T.A.B.D. Sanjeewa ◽  
D.K.N.G. Pushpakumara ◽  
U.R. Sangakkara

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


2020 ◽  
Vol 13 (11) ◽  
pp. 1
Author(s):  
A. R. B. Zanco ◽  
A. Ferreira ◽  
G. C. M. Berber ◽  
E. N. Gonzaga ◽  
D. C. C. Sabino

The different integrated production systems can directly interfere with its bacterial community. The present study aimed to assess density, bacterial diversity and the influence of dry and rainy season in different integrated and an exclusive production system. The fallow and a native forest area was assessed to. Samples were collected in 2012 March and September. The isolation were carried out into Petri dishes containing DYGS medium. The number of colony forming units (CFU) was counted after 48 hours and. The bacterial density ranged between 106 and 107 CFU g-1 soil. The crop system affected the dynamics of the bacterial community only in the rainy season. The rainy season showed greater density of total bacteria when compared to the dry period regardless of the cropping system. The dendrograms with 80 % similarity showed thirteen and fourteen groups in the rainy and dry seasons. Isolates with the capacity to solubilize phosphate in vitro were obtained from all areas in the two seasons, but this feature has been prevalent in bacteria isolated during the rainy season


2020 ◽  
Vol 20 (4) ◽  
pp. 448-454
Author(s):  
Rahmita Burhamzah ◽  
Gemini Alam ◽  
Herlina Rante

Background: Endophytic fungi live in plants’ tissue and can produce the same bioactive compounds as its host plant produces. Syzygiumpolyanthum leaves have known to be one of the antibacterial compound producers. Aim and Objective: This study aimed to characterize morphologically, microscopically, and molecularly the antibacterial-producing endophytic fungi of Syzygiumpolyanthum leaves. Methods: The isolation of endophytic fungi was done by fragment planting method on PDA medium. The antibacterial screening was performed using the antagonistic test as the first screening followed by the disc diffusion test method. The morphological characterization was based on isolate’s mycelia color, growth pattern, margin, and surface texture of the colony, while the microscopic characterization was based on its hyphae characteristics. The molecular characterization of the isolate was done by nitrogen base sequence analysis method on nucleotide constituent of ITS rDNA genes of the isolate. Results: The results found that isolate DF1 has antibacterial activity against E.coli, S.aureus, P.acne, and P.aeruginosa, with the greatest inhibition at 10% concentration of broth fermentation extract on S.aureus with a diameter of inhibition of 13.77 mm. Conclusion: Based on macroscopic, microscopic, and molecular characterization, DF1 isolate is similar to Ceriporialacerate.


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