scholarly journals Large-scale Phenotypic Profiling of Gene Deletion Mutants in Candida glabrata

BIO-PROTOCOL ◽  
2015 ◽  
Vol 5 (14) ◽  
Author(s):  
Fabian Istel ◽  
Tobias Schwarzm�ller ◽  
Michael Tscherner ◽  
Karl Kuchler
2015 ◽  
Vol 11 (11) ◽  
pp. 3129-3136 ◽  
Author(s):  
Namal V. C. Coorey ◽  
James H. Matthews ◽  
David S. Bellows ◽  
Paul H. Atkinson

Identifying Saccharomyces cerevisiae genome-wide gene deletion mutants that confer hypersensitivity to a xenobiotic aids the elucidation of its mechanism of action (MoA).


2019 ◽  
Vol 18 (1) ◽  
Author(s):  
Fulu Liu ◽  
Yating Zhang ◽  
Wanjin Qiao ◽  
Duolong Zhu ◽  
Haijin Xu ◽  
...  

Abstract Background After 2.83% genome reduction in Lactococcus lactis NZ9000, a good candidate host for proteins production was obtained in our previous work. However, the gene deletion process was time consuming and laborious. Here, we proposed a convenient gene deletion method suitable for large-scale genome reduction in L. lactis NZ9000. Results Plasmid pNZ5417 containing a visually selectable marker PnisZ-lacZ was constructed, which allowed more efficient and convenient screening of gene deletion mutants. Using this plasmid, two large nonessential DNA regions, L-4A and L-5A, accounting for 1.25% of the chromosome were deleted stepwise in L. lactis 9k-3. When compared with the parent strain, the mutant L. lactis 9k-5A showed better growth characteristics, transformability, carbon metabolic capacity, and amino acids biosynthesis. Conclusions Thus, this study provides a convenient and efficient system for large-scale genome deletion in L. lactis through application of visually selectable marker, which could be helpful for rapid genome streamlining and generation of restructured L. lactis strains that can be used as cell factories.


2009 ◽  
Vol 30 (3) ◽  
pp. E500-E519 ◽  
Author(s):  
Paola S. Denora ◽  
David Schlesinger ◽  
Carlo Casali ◽  
Fernando Kok ◽  
Alessandra Tessa ◽  
...  
Keyword(s):  

3 Biotech ◽  
2017 ◽  
Vol 7 (3) ◽  
Author(s):  
Payal Gupta ◽  
Ramesh Chand Meena ◽  
Navin Kumar

Metallomics ◽  
2016 ◽  
Vol 8 (5) ◽  
pp. 542-550 ◽  
Author(s):  
Adam J. Johnson ◽  
Filip Veljanoski ◽  
Patrick. J. O'Doherty ◽  
Mohammad S. Zaman ◽  
Gayani Petersingham ◽  
...  

2010 ◽  
Vol 76 (8) ◽  
pp. 2425-2432 ◽  
Author(s):  
Christine M. Fennessey ◽  
Morris E. Jones ◽  
Martial Taillefert ◽  
Thomas J. DiChristina

ABSTRACT Shewanella oneidensis MR-1 respires a wide range of anaerobic electron acceptors, including sparingly soluble Fe(III) oxides. In the present study, S. oneidensis was found to produce Fe(III)-solubilizing organic ligands during anaerobic Fe(III) oxide respiration, a respiratory strategy postulated to destabilize Fe(III) and produce more readily reducible soluble organic Fe(III). In-frame gene deletion mutagenesis, siderophore detection assays, and voltammetric techniques were combined to determine (i) if the Fe(III)-solubilizing organic ligands produced by S. oneidensis during anaerobic Fe(III) oxide respiration were synthesized via siderophore biosynthesis systems and (ii) if the Fe(III)-siderophore reductase was required for respiration of soluble organic Fe(III) as an anaerobic electron acceptor. Genes predicted to encode the siderophore (hydroxamate) biosynthesis system (SO3030 to SO3032), the Fe(III)-hydroxamate receptor (SO3033), and the Fe(III)-hydroxamate reductase (SO3034) were identified in the S. oneidensis genome, and corresponding in-frame gene deletion mutants were constructed. ΔSO3031 was unable to synthesize siderophores or produce soluble organic Fe(III) during aerobic respiration yet retained the ability to solubilize and respire Fe(III) at wild-type rates during anaerobic Fe(III) oxide respiration. ΔSO3034 retained the ability to synthesize siderophores during aerobic respiration and to solubilize and respire Fe(III) at wild-type rates during anaerobic Fe(III) oxide respiration. These findings indicate that the Fe(III)-solubilizing organic ligands produced by S. oneidensis during anaerobic Fe(III) oxide respiration are not synthesized via the hydroxamate biosynthesis system and that the Fe(III)-hydroxamate reductase is not essential for respiration of Fe(III)-citrate or Fe(III)-nitrilotriacetic acid (NTA) as an anaerobic electron acceptor.


2008 ◽  
Vol 9 (9) ◽  
pp. R140 ◽  
Author(s):  
Evan S Snitkin ◽  
Aimée M Dudley ◽  
Daniel M Janse ◽  
Kaisheen Wong ◽  
George M Church ◽  
...  

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