PHOTOBIOLOGICAL CHARACTERIZATION OF A SPORE GERMINATION MUTANT dkgl WITH REVERSED PHOTOREGULATION IN THE FERN Ceratopteris richardii

1993 ◽  
Vol 57 (s1) ◽  
pp. 1032-1041 ◽  
Author(s):  
Todd J. Cooke ◽  
Leslie G. Hickok ◽  
William J. VANDERWOUDE ◽  
Jo Ann Banks ◽  
Rodney J. Scott
2007 ◽  
Vol 97 (2) ◽  
pp. 47-65 ◽  
Author(s):  
Rodney J. Scott ◽  
Gerald J. Gastony ◽  
Jeremy W. Weatherford ◽  
Takuya Nakazato

2007 ◽  
Vol 71 (4) ◽  
pp. 986-992 ◽  
Author(s):  
Yuu AOKI ◽  
Masahiro YOSHIDA ◽  
Hiroshi KAWAIDE ◽  
Hiroshi ABE ◽  
Masahiro NATSUME

2010 ◽  
Vol 11 (4) ◽  
pp. 503-512 ◽  
Author(s):  
JIE FENG ◽  
RU HWANG ◽  
SHEAU-FANG HWANG ◽  
STEPHEN E. STRELKOV ◽  
BRUCE D. GOSSEN ◽  
...  

1981 ◽  
Vol 4 (1) ◽  
pp. 29-36 ◽  
Author(s):  
Andreas Hartig ◽  
Ren�e Schroeder ◽  
Eva Mucke ◽  
Michael Breitenbach

2000 ◽  
Vol 182 (9) ◽  
pp. 2513-2519 ◽  
Author(s):  
Madan Paidhungat ◽  
Peter Setlow

ABSTRACT Dormant Bacillus subtilis spores germinate in the presence of particular nutrients called germinants. The spores are thought to recognize germinants through receptor proteins encoded by the gerA family of operons, which includesgerA, gerB, and gerK. We sought to substantiate this putative function of the GerA family proteins by characterizing spore germination in a mutant strain that contained deletions at all known gerA-like loci. As expected, the mutant spores germinated very poorly in a variety of rich media. In contrast, they germinated like wild-type spores in a chemical germinant, a 1-1 chelate of Ca2+ and dipicolinic acid (DPA). These observations showed that proteins encoded bygerA family members are required for nutrient-induced germination but not for chemical-triggered germination, supporting the hypothesis that the GerA family encodes receptors for nutrient germinants. Further characterization of Ca2+–DPA-induced germination showed that the effect of Ca2+–DPA on spore germination was saturated at 60 mM and had a Km of 30 mM. We also found that decoating spores abolished their ability to germinate in Ca2+–DPA but not in nutrient germinants, indicating that Ca2+–DPA and nutrient germinants probably act through parallel arms of the germination pathway.


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