Bacillus clausii
A Microbial Biorealm page on the genus Bacillus clausii
Classification
Higher order taxa
Eubacteria (kingdom); Bacteria (domain); Firmicutes (phylum); Bacilli (class); Bacillales (order); Bacillaceae (family); Bacillus (genus)
Species
Bacillus clausii
Description and significance
Describe the appearance, habitat, etc. of the organism, and why it is important enough to have its genome sequenced. Describe how and where it was isolated. Include a picture or two (with sources) if you can find them.
Bacillus clausii is Gram positive, motile, spore-forming and like most of the Bacillus bacteria, it is rod-shaped. Colonies of B. clausii form filamentous margins that appear cream-white in color. B. clausii is alkaliphilic and produces a class of subtilisins known as high-alkaline proteases. The protease from Bacillus clausii strain 221, the H-221 protease, was the first enzyme to be identified in an alkaliphilic Bacillus. [Kageyama] The alkaliphilic nature of the organism has also proved it to be useful in preventing and treating various gastrointestinal disorders as an oral bacteriotherapy. [Senesi] This organism can be found in many alkaline environments, including soil and marine habitat.
The B. clausii strain KSM-K16 was obtained from soil samples, and its phylogenic position as a member of B. clausii was identified using Bacillus clausii DSM8716 as a reference strain. The techniques used to determine the classification included 16S rRNA sequencing, which directly compares two or more strains of rRNA sequences to determine sequence homology. Other classification techniques including fatty acid analysis, which identifies fatty acids in the membrane, and carbohydrate utilization tests, which establish the metabolic characteristics of the organism. Growth of KSM-K16 was observed in the temperature range of 15-50°C and the pH range of 7-10.5, with optimal growth at 40°C and pH 9.0. The KSM-K16 strain produces the high-alkaline protease, M-protease, which is hyperproduced by a mutant to be used in industrial scale compact heavy-duty laundry detergent. This protease, amoung other enzymes utilized by B. clausii organisms, are being extensively studied to understand their ability to function in such alkaline conditions for possible biotechnology use, making the genome of B. clausii a necessary tool.[Kageyama]
http://www.springerlink.com/content/f6h65u65125t4811/fulltext.html http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=92655
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstract&list_uids=7632397
Genome structure
Describe the size and content of the genome. How many chromosomes? Circular or linear? Other interesting features? What is known about its sequence? Does it have any plasmids? Are they important to the organism's lifestyle?
The Bacillus clausii KSM-K16 complete genome is one circular chromosome composed of 4,303,871 nucleotides. The genome represents 4204 genes, of which 4096 are protein coding and 96 code for RNAs. The GC content of B. clausii KSM-K16 is 44%.
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=565
Cell structure and metabolism
Describe any interesting features and/or cell structures; how it gains energy; what important molecules it produces.
Bacillus clausii is a rod shaped, gram-positive microbe, meaning it is surrounded by a thick cell wall. The cell wall is made up of the peptidoglycan murien, which is composed of a mixture of sugars and proteins.
Ecology
Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.
Pathology
Bacillus clausii resistance to many antibiotics makes it seem capable of harm to humans, but Bacillus clausii sporulated strains are actually used in the treatment of gastrointestinal illnesses to restore intestinal flora because of their antibiotic resistance and ability to stimulate immune activity (see Application to Biotechnology).
Application to Biotechnology
Does this organism produce any useful compounds or enzymes? What are they and how are they used?
B. clausii genome sequence is being studied for its importance in biotechnology:
"[Bacillus clausii and other relatives] are now being investigated in order to better understand the physiology, biochemistry, and especially molecular genetics underlying the behavior of alkaliphilic bacteria . Most of the studies have been performed to examine enzyme biotechnology, as alkaliphilic Bacillus strains produce enzymes, such as xylanases, cellulases, amylases, and proteases, that are very useful in industry and domestic life" [Senesi]
B. clausii strain KSM-K16, for example, produces especially useful proteases known as of M, H, and N-proteases. A proteolytic enzyme cleaves polypeptides into smaller pieces of amino acids. Like other Bacillus organisms, KSM-K16 secretes its proteases directly into the medium, especially during periods of low nutrition, coupled with the process of sporulation. The control of protease release has been studied in more detail with Bacillus subtilis. B. subtilis studies has shown that regulatory events during periods of cellular stress can lead to a cascade of events that include the increased release of proteloytic enzymes; more specifically, the regulatory phoshorylation of the transcription factor Spo0A inhibits the repression of a gene that encodes the B. subtilis protease. Microbial control of M-protease is similarly studied to implement for industrial use for mass production by B. claussi strain KSM-K16.
This most extensively studied protease produced by KSM-K16, M-protease, is used in heavy-duty detergents to remove protein containing spots from laundry. M-protease has a maximum enzyme activity at pH 12.3 and 55°C in phosphate-NaOH buffer. The ability for M-protease to function at such high pH was remarkable, and the enzyme characteristics were studied to determine what modifications exist on the structural level of the protein to enable its viability in such alkaline conditions, using X-ray crystallography and genome sequencing. Results indicated that the unique protease contained a lower number of negatively charged amino acids and lysine residues, with an increase in arginine and nuetral amino acids than proteases not adapted to such alkaline environments. This in effect increases the isoelectric point of the enzyme to enable its function in high pH.
With this important information, bioengineers can design novel proteins in the lab to be used in such extreme conditions. For example, alkaline proteases are currently finding newer uses, including their usage to create useful biomass from fibrous proteins such as horn, feather or hair. A couple other uses include hydrolysis of gelatine layers of X-ray films and the recovery of silver.
http://peds.oxfordjournals.org/cgi/reprint/10/6/627
http://www.blackwell-synergy.com/doi/full/10.1046/j.1365-2672.2003.02153.x?cookieSet=1
The spores of B. clausii and other related Bacilli are used as probiotics to improve the intestinal microbial balance during periods of antibiotic usage, modify the immune system function of the GI tract, and act as anti-microbial agents themselves. Probiotic-containing treatments are available for human nutrition, animal feed supplements, and also for aquaculture. An antibiotic resistant probiotic known as Enterogermina consists of 4 strains of Bacillus microbes (O/C, N/R, SIN, and T), all of which were recently reclassified from subtilis to clausii. Enterogermina is notably used in the treatment of diarrhea and prevention of infectious gastrointestinal diseases. Though not completely understood, the enzyme secretions of B. clausii during sporulation are believed to lead to these positive effect on the GI tract; during sporulation, strains from Enterogermina were found to release antimicrobial compounds and modulate immune activity. With further knowledge of the function of B. clausii activity as Enterogermina, the usage of this mibrobe in medicine can be optimized and implemented in more effective ways.
http://www.pubmedcentral.nih.gov/botrender.fcgi?blobtype=html&artid=383048
Current Research
Research performed by Bülent Bozdogan at the Service de Microbiologie in Caen, France has revealed a 846 base pair erm-related gene in Bacillus clausii that confers resistance to certain antibiotics. Erm proteins are ribosomal methylases that methylate monomethylate or dimethylate a certain adenine in 23S rRNA, which when methylated could bind macrolides (antibiotics) such as erythromycin, azithromycin, spiramycin, lincomycin, clindamycin, and pristinamycin I. This erm-related gene in B. clasii strain DSM 8716 was named erm(34). http://aem.asm.org/cgi/content/full/70/1/280
The process of by which Enterogermina strains of B. clausii alleviate gastrointestinal disorder is not completely understood. Gabriella Casula and Simon M. Cutting of the Royal Holloway University of London have developed a method to study colonization characteristics of Enterogermina in mouse gut. They have shown that B. clausii in Enterogermina can in fact colonize for brief periods of time on the intestinal wall of the gut, and provoke immune response in mice to rid of pathogenic bacteria. Studies such as these can shed light on the mechanism of gastrointestinal revival and protection induced by Enterogermina supplementation.
http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pubmed&pubmedid=11976107
M-protease from B. clausii KSM-K16 is still heavily studied to determine the unique structural components that allow its function at such high pH. A recent study by Kobayashi and Kageyama from the Tochigi Research Laboratories in Japan have revealed a salt bridge triad (Arg19–Glu271–Arg275) that exists in M-protease but not in proteases that cannot withstand such alkaline conditions. This slat bridge was found to increase the thermostability of the enzyme at such high pH. Findings such as these are furthering our knowledge of alkaline-adapted enzymes for the possible utilization in novel enzyme engineering. http://www.springerlink.com/content/7531q167636108l4/
References
Though not formally written in here, the references have been marked throughout so far to make sure I know where I obtained each source.
Edited by Ankur Patel of Rachel Larsen and Kit Pogliano
