FEMS Special Merit Award
The FEMS Special Merit Award was initiated in 2003 to reward those who have made special contributions to further the objectives of FEMS. The first award was presented at the 1st FEMS Congress in 2003.
This award acknowledges and honours extraordinary services rendered to FEMS at the organizational, structural and/or administrative level.
The award comes in the form of an illuminated address featuring the awardee’s name and his/her special merits for FEMS.
The award may be given to those persons who have (altruistically) contributed to the organizational, structural and/or administrative improvements of the Federation. FEMS (former) Directors are not eligible.
The award may be given at any time and frequency.
Proposals may be submitted at any time and there is no deadline. Candidates may be proposed by a FEMS Delegate on behalf of their FEMS Member Society or by members of the FEMS Board of Directors. Proposals should be submitted to the Convenor of the Awards Board via FEMS Business Office and consist of:
- a letter of recommendation written by the promoter or the Member Society
- a listing of special merits for FEMS
- a curriculum vitae (max. 2 pages) and list of achievements
FEMS Special Merit Awardee 2003
Ir Lex (W.A.) Scheffers
Special Merit: (I) Structural inputs to the Federation over a period of seven years as FEMS Delegate; (II) Organisational inputs in establishing FEMS Central Office; (III) Founding a new FEMS journal ‘FEMS Yeast Research’ and achieving high scientific standards from its onset. (photo collage)
Venue: Ljubljana, Slovenia, at the occasion of the 1st FEMS Congress.
Date: 2 July 2003
Two methods are described for efficient genetic modification of Saccharomyces cerevisiae using CRISPR/Cas9. The first method enables the modification of a single genetic locus using in vivo assembly of a guide RNA (gRNA) expression plasmid without the need for prior cloning. A second method using in vitro assembled plasmids that could contain up to two gRNAs was used to simultaneously introduce up to six genetic modifications (e.g. six gene deletions) in a single transformation step by transforming up to three gRNA expression plasmids simultaneously. The method is not only suitable for gene deletion but is also applicable for in vivo site-directed mutagenesis and integration of multiple DNA fragments in a single locus.