Formation of Protoplasts from Cultured Tobacco Cells and Arabidopsis thaliana by the Action of Cellulosomes and Pectate Lyase from Clostridium cellulovorans
Open Access
- 1 May 2002
- journal article
- research article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 68 (5) , 2614-2618
- https://doi.org/10.1128/aem.68.5.2614-2618.2002
Abstract
The crude culture supernatants from Clostridium cellulovorans were tested for their ability to convert plant cells to protoplasts. The supernatants readily released protoplasts from cultured tobacco cells and Arabidopsis thaliana . The crude culture supernatant from pectin-grown cells was more active than supernatants from glucose-, cellobiose-, xylan-, and locust bean gum-grown cells. After removal of cellulosomes, the crude culture supernatant lost its protoplast formation activity. The protoplast formation activity of the crude culture supernatant from C. cellulovorans was more effective than those of commercial enzymes based on protein content.Keywords
This publication has 26 references indexed in Scilit:
- Determination of Subunit Composition of Clostridium cellulovorans Cellulosomes That Degrade Plant Cell WallsApplied and Environmental Microbiology, 2002
- Characterization of Xylanolytic Enzymes in Clostridium cellulovorans : Expression of Xylanase Activity Dependent on Growth SubstratesJournal of Bacteriology, 2001
- The engL Gene Cluster of Clostridium cellulovorans Contains a Gene for Cellulosomal ManAJournal of Bacteriology, 2000
- Characterization of engF, a gene for a non-cellulosomal Clostridium cellulovorans endoglucanaseGene, 1996
- A kinesin-like protein, KatAp, in the cells of arabidopsis and other plants.Plant Cell, 1996
- Synthesis, assembly and function of plant cell wall macromoleculesCurrent Opinion in Cell Biology, 1992
- Nucleotide sequence and characteristics of endoglucanase gene engB from Clostridium cellulovoransJournal of General Microbiology, 1991
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970