scholarly journals In Vivo Screening for Biocontrol Agents (BCAs) against Streptomyces scabiei Causing Potato Common Scab

2004 ◽  
Vol 20 (2) ◽  
pp. 110-114 ◽  
Author(s):  
Hyang-Burm Lee ◽  
Jong-Wun Cho ◽  
Dong-Jin Park ◽  
Chang-Tian Li ◽  
Young-Hwan Ko ◽  
...  
Keyword(s):  
Common Scab ◽  
Biocontrol Agents ◽  
In Vivo Screening ◽  
Potato Common Scab ◽  
Streptomyces Scabiei

scholarly journals Isolation and structural properties of aerial mycelium differentiation-inhibitory substances against Streptomyces scabiei causing potato common scab

2007 ◽  
Vol 32 (2) ◽  
pp. 131-134
Author(s):  
Masahiro Natsume ◽  
Atsushi Ooshiro ◽  
Tsuneki Takahashi ◽  
Fumihiko Kokido ◽  
Makoto Hashimoto ◽  
...  
Keyword(s):  
Structural Properties ◽  
Common Scab ◽  
Aerial Mycelium ◽  
Potato Common Scab ◽  
Streptomyces Scabiei

scholarly journals Genomic and Metabolomic Analysis of the Potato Common Scab Pathogen Streptomyces scabiei

ACS Omega ◽  
2021 ◽  
Vol 6 (17) ◽  
pp. 11474-11487
Author(s):  
Jingyu Liu ◽  
Louis-Félix Nothias ◽  
Pieter C. Dorrestein ◽  
Kapil Tahlan ◽  
Dawn R. D. Bignell
Keyword(s):  
Common Scab ◽  
Metabolomic Analysis ◽  
Potato Common Scab ◽  
Streptomyces Scabiei

scholarly journals Antimicrobial Activity against Potato Common Scab (Streptomyces scabiei) of Green Manure Crop Extracts

2011 ◽  
Vol 24 (5) ◽  
pp. 622-627 ◽  
Author(s):  
Jong-In Park ◽  
Hee-Jeong Jung ◽  
Yong-Hui Bae ◽  
Kwon-Kyoo Kang ◽  
Ill-Sup Nou
Keyword(s):  
Antimicrobial Activity ◽  
Green Manure ◽  
Common Scab ◽  
Green Manure Crop ◽  
Potato Common Scab ◽  
Streptomyces Scabiei

scholarly journals Suberin Regulates the Production of Cellulolytic Enzymes in Streptomyces scabiei, the Causal Agent of Potato Common Scab

2015 ◽  
Vol 30 (3) ◽  
pp. 245-253 ◽  
Author(s):  
Rebeca Padilla-Reynaud ◽  
Anne-Marie Simao-Beaunoir ◽  
Sylvain Lerat ◽  
Mark A. Bernards ◽  
Carole Beaulieu
Keyword(s):  
Common Scab ◽  
Causal Agent ◽  
Cellulolytic Enzymes ◽  
Potato Common Scab ◽  
Streptomyces Scabiei

scholarly journals Canadian goldenrod residues and extracts inhibit the growth of Streptomyces scabiei, the causal agent of potato common scab

2017 ◽  
Vol 40 (1) ◽  
pp. 70-75 ◽  
Author(s):  
Maxime C. Paré ◽  
Jean Legault ◽  
André Pichette ◽  
Catherine Tremblay ◽  
Marie-France Aubut
Keyword(s):  
Common Scab ◽  
Causal Agent ◽  
Potato Common Scab ◽  
Streptomyces Scabiei

scholarly journals Draft Genome Sequences of Streptomyces scabiei S58, Streptomyces turgidiscabies T45, and Streptomyces acidiscabies a10, the Pathogens of Potato Common Scab, Isolated in Japan: TABLE 1 

2016 ◽  
Vol 4 (2) ◽  
Author(s):  
Tsuyoshi Tomihama ◽  
Yatsuka Nishi ◽  
Masao Sakai ◽  
Makoto Ikenaga ◽  
Takashi Okubo ◽  
...  
Keyword(s):  
Genome Size ◽  
Common Scab ◽  
Draft Genome ◽  
Pathogenicity Island ◽  
Genome Sequences ◽  
Potato Common Scab ◽  
Streptomyces Turgidiscabies ◽  
Streptomyces Acidiscabies ◽  
Streptomyces Scabiei

The draft genome sequences of the three pathogens of potato common scab, Streptomyces scabiei S58, Streptomyces turgidiscabies T45, and Streptomyces acidiscabies a10, isolated in Japan, are presented here. The genome size of each strain is >10 Mb, and the three pathogenic strains share genes located in a pathogenicity island previously described in other pathogenic Streptomyces species.

Synthesis of Novel 3(N,N-dialkylamino)alkyl/phenyl Substituted Thieno [2,3-d]pyrimidinones as H1-Anti-Histaminic and Antimicrobial Agents

2019 ◽  
Vol 15 (1) ◽  
pp. 63-70
Author(s):  
Shiv Dev Singh ◽  
Arvind Kumar ◽  
Firoz Babar ◽  
Neetu Sachan ◽  
Arun Kumar Sharma
Keyword(s):  
Antimicrobial Activity ◽  
Potassium Hydroxide ◽  
Antimicrobial Agents ◽  
Pyrimidine Ring ◽  
Antimicrobial Activities ◽  
Screening Methods ◽  
Chlorpheniramine Maleate ◽  
In Vivo Screening

Background: Thienopyrimidines are the bioisoster of quinazoline and unlike quinazoline exist in three isomeric forms corresponding to the three possible types annulation of thiophene to the pyrimidine ring viz thieno[2,3-d] pyrimidine, thieno[3,2-d] pyrimidine and thieno[3,4-d]pyrimidine. Heterocyclic containing the thienopyrimidinone moiety exhibits various pronounced activities such as anti-hypertensive, analgesic and anti-inflammatory, antiviral, platelet aggregation inhibitory, antiprotozoal bronchodilatory, phosphodiesterase inhibitory, antihistaminic, antipsychotic and antimicrobial activity. Objective: Synthesis of novel 3(N,N-dialkylamino)alkyl/phenyl substituted thieno[2,3-d]pyrimidinones as H1-anti-histaminic and antimicrobial agents. Methods: A series of 3-[(N,N-dialkylamino)alkyl/phenyl]-2-(1H)thioxo-5,6,7,8-tetrahydrobenzo(b) thieno(2,3-d)pyrimidine-4(3H)-ones[4a-d], their oxo analogous [5a-d] and 3-[(N,N-dialkylamino)alkyl]- 2-chlorophenyl-5,6,7,8-tetrahydrobenzo(b)thieno(2,3-d)pyrimidine- 4 (3H)-ones[6a-d]derivative were synthesized from 2-amino-4,5,6,7-tetrahydrobenzo(b)thiophene-3-carboxylic acid by nucleophilic substitution of different N,N-dialkyl alkylene/phenylene diamines on activated 3-acylchloride moiety followed by cyclocondensation with carbon disulfide and ethanolic potassium hydroxide to get [4a-d] and in second reaction by condensation with 4-chlorobenzoyl chloride to get [6a-d] by single pot novel innovative route. The oxo analogous [5a-d] were prepared by treating derivatives [4a-d] with potassium permagnate in ethanolic KOH. The synthesized compound were evaluated for H1-antihistaminic and antimicrobial activities. Results: All synthesized compounds exhibited significant H1-antihistaminic activity by in vitro and in vivo screening methods and data were verified analytically and statistically. The compound 4a, 4b, 5a and 5b showed significant H1-antihistaminiic activity than the reference standard chlorpheniramine maleate. The compound 6d, 6c, 5c and 4c exhibited significant antimicrobial activity.

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