Colonial variation in Xanthomonas campestris NRRL B-1459 and characterization of the polysaccharide from a variant strain

1976 ◽  
Vol 22 (7) ◽  
pp. 942-948 ◽  
Author(s):  
M. C. Cadmus ◽  
S. P. Rogovin ◽  
K. A. Burton ◽  
J. E. Pittsley ◽  
C. A. Knutson ◽  
...  

Stock cultures of Xanthomonas campestris NRRL B-1459 require special attention to maintenance and propagation to assure consistent production in good yields of the extracellular polysaccharide xanthan. Under customary conditions of propagative maintenance on agar slants, variant colony types develop that are smaller in size than the normal type. The rate of regression of the normal to the variant forms was diminished when the D-glucose content of the stock medium was sufficient to avoid depletion during storage and when transfer to fresh medium was reduced to 14-day intervals. Under conditions for polysaccharide production, the normal large-colony type gives crude culture liquors after 48 h of 7000 centipoise (cp) viscosity; the predominant variant form gives only 4000 cp. On the basis of 2.1% initial D-glucose, biopolymer yields for the normal and variant strains were 62 and 43%, respectively. Polysaccharide produced by the variant (small-colony type) differs adversely in solution properties from that of the parent strain (large-colony type); it differs also in its lower content of pyruvic acid and O-acetyl substituents. The molar ratios of constituent sugars (D-glucose, D-mannose, and D-glucuronic acid), however, were identical in polysaccharides with the normal and variant strains. Exclusion of colonial variants from fermentations is prerequisite to production of xanthan optimum in properties and yield.

1988 ◽  
Vol 34 (8) ◽  
pp. 1017-1022 ◽  
Author(s):  
Jeffrey S. La Favre ◽  
Adrienne K. La Favre ◽  
Allan R. J. Eaglesham

Bradyrhizobium japonicum strain USDA 76, a rhizobitoxine producer, was found to contain two colony types, designated "small" and "large" based on colony size on agar medium. Only the small type produced detectable chlorosis-inducing toxin in culture, whereas both colony types induced chlorosis as a result of synthesis of toxin in nodules. Electron microscopy revealed that a large colony derivative, grown in broth culture, was encapsulated, whereas a small colony derivative was not, suggesting a negative functional relationship between toxin synthesis and presence of capsule. The large type also had a ruthenium red reactive extracellular layer when cultured in the soybean rhizosphere. This differential production of toxin by the colony derivatives in culture, and presumably in the rhizosphere, prompted the investigation of a proposed role of rhizobitoxine in the infection of roots of nodulation-refractory (rj1rj1) soybean; the small colony type formed fewer nodules on the (rj1rj1) isoline, indicating no major function for rhizobitoxine in the infection of (rj1rj1) soybean.


Microbiology ◽  
1996 ◽  
Vol 142 (12) ◽  
pp. 3515-3524 ◽  
Author(s):  
X. Cheng ◽  
J. Nicolet ◽  
R. Miserez ◽  
P. Kuhnert ◽  
M. Krampe ◽  
...  

1972 ◽  
Vol 18 (7) ◽  
pp. 969-973 ◽  
Author(s):  
Stephen Shugar ◽  
Kenneth E. Sanderson

A spontaneous mutant of Escherichia coli K12 C600 was isolated which is mucoid as a result of overproduction of an extracellular polysaccharide. This strain also forms filaments, is sensitive to ultraviolet irradiation, and has its genetic lesion closely linked to the lac gene. Its phenotype and map position are analogous to the lon mutation (long form). The exopolysaccharide contains fucose, glucose, galactose, and may contain glucuronic acid, but the molar ratios of these sugars differ from those previously reported.


2001 ◽  
Vol 183 (4) ◽  
pp. 1195-1204 ◽  
Author(s):  
Eric Déziel ◽  
Yves Comeau ◽  
Richard Villemur

ABSTRACT Pseudomonas aeruginosa is a ubiquitous environmental bacterium capable of forming biofilms on surfaces as a survival strategy. It exhibits a large variety of competition/virulence factors, such as three types of motilities: flagellum-mediated swimming, flagellum-mediated swarming, and type IV pilus-mediated twitching. A strategy frequently used by bacteria to survive changing environmental conditions is to create a phenotypically heterogeneous population by a mechanism called phase variation. In this report, we describe the characterization of phenotypic variants forming small, rough colonies that spontaneously emerged when P. aeruginosa 57RP was cultivated as a biofilm or in static liquid cultures. These small-colony (S) variants produced abundant type IV fimbriae, displayed defective swimming, swarming, and twitching motilities, and were impaired in chemotaxis. They also autoaggregated in liquid cultures and rapidly initiated the formation of strongly adherent biofilms. In contrast, the large-colony variant (parent form) was poorly adherent, homogeneously dispersed in liquid cultures, and produced scant polar fimbriae. Further analysis of the S variants demonstrated differences in a variety of other phenotypic traits, including increased production of pyocyanin and pyoverdine and reduced elastase activity. Under appropriate growth conditions, cells of each phenotype switched to the other phenotype at a fairly high frequency. We conclude that these S variants resulted from phase variation and were selectively enriched when P. aeruginosa 57RP was grown as a biofilm or in static liquid cultures. We propose that phase variation ensures the prior presence of phenotypic forms well adapted to initiate the formation of a biofilm as soon as environmental conditions are favorable.


1977 ◽  
Vol 23 (9) ◽  
pp. 1118-1122 ◽  
Author(s):  
Robert G. Upchurch ◽  
Gerald H. Elkan

Four strains of Rhizobium japonicum, two of which produce slimy and non-slimy colony types and two others which produce large and small colony types, were isolated and cloned. All were infective and nodulated Lee soybean host plants. Each colony type was characterized as to its salt sensitivity to Na+ and K+ ions, relative level of symbiotic nitrogen fixation, and relative level of free-living nitrogen fixation. Growth studies performed in the presence of salts demonstrated that the non-slimy or small colony types were sensitive to salt with significantly depressed growth rates and cell yields. Growth rates and cell yields of slimy, large, colony types were relatively unaffected by salt. Both symbiotic and free-living (non-associative) nitrogen fixation analyses (by acetylene reduction) revealed that the non-slimy, small colonies were significantly more effective than slimy, large colonies.


2008 ◽  
Vol 76 (4) ◽  
pp. 1485-1497 ◽  
Author(s):  
Brenda L. Grau ◽  
Margaret C. Henk ◽  
Katherine L. Garrison ◽  
Brett J. Olivier ◽  
Randall M. Schulz ◽  
...  

ABSTRACT Capsular polysaccharide (CPS) is a major virulence factor in Vibrio vulnificus, and encapsulated strains have an opaque, smooth (OpS) colony morphology, while nonencapsulated strains have a translucent, smooth (TrS) colony morphology. Previously, we showed that OpS and TrS parental strains can yield a third colony type, rugose (R), and that the resulting strains, with the OpR and TrR phenotypes, respectively, form copious biofilms. Here we show that while OpR and TrR strains both produce three-dimensional biofilm structures that are indicative of rugose extracellular polysaccharide (rEPS) production, OpR strains also retain expression of CPS and are virulent in an iron-supplemented mouse model, while TrR strains lack CPS and are avirulent. Chlorine resistance assays further distinguished OpR and TrR isolates as exposure to 3 μg/ml NaOCl eradicated both OpS and OpR strains, while both TrS and TrR strains survived, but at rates which were significantly different from one another. Taken together, these results further emphasize the importance of CPS for virulence of V. vulnificus and establish a correlation between CPS expression and chlorine sensitivity in this organism. Using reverse transcriptase PCR, we also identified a nine-gene cluster associated with both CPS and rEPS expression in V. vulnificus, designated the wcr (capsular and rugose polysaccharide) locus, with expression occurring primarily in R variants. The latter results set the stage for characterization of functional determinants which individually or collectively contribute to expression of multiple EPS forms in this pathogen.


1984 ◽  
Vol 93 (3) ◽  
pp. 465-473 ◽  
Author(s):  
M. Kanyi Kibe ◽  
G. R. Smith

SummaryIn vivo methods were used to study the F38-type mycoplasma in parallel with related mycoplasmas.Three of five strains of ‘bovine serogroup 7’ with an unknown history of subculture produced mycoplasmaemia in mice inoculated intraperitoneally. A strain of ‘bovine serogroup L’ also produced mycoplasmaemia, but no evidence of similar ability could be found for single strains of Mycoplasma capricolum, M. equigenitalium and M. primatum, or for two strains of the F38-type mycoplasma.In cross-immunization tests a bovine serogroup 7 strain (NCTC 10133) and a strain (‘Blenheim’) of the SC (small colony) type of M. mycoides subsp. mycoides were used for the purpose of challenge. Cross-protection was described as ‘complete’ or ‘partial’, depending on whether it was as great as, or less than, that produced by homologous vaccine. Although strain NCTC 10133 protected strongly, possibly completely, against Blenheim, and Blenheim gave partial protection against NCTC 10133, challenge with NCTC 10133 and Blenheim gave strikingly different results. Thus (1) F38-type strains, M equigenitalium and M. primatum all gave partial cross-protection against NCTC 10133 but not against Blenheim, (2) NCTC 10133, unlike Blenheim, was seldom susceptible to partial cross-protection by LC (large colony) strains of M. mycoides subsp. mycoides, and (3) three SC strains – which would have protected completely against Blenheim – protected only partially against NCTC 10133. NCTC 10133 and Blenheim were similar, however, in that M. capricolum and M. mycoides subsp. capri failed to cross-protect against them both.


1956 ◽  
Vol 11 (6) ◽  
pp. 317-329 ◽  
Author(s):  
P. Starlinger ◽  
F. Kaudewitz

In Salmonella typhimurium, UV-irradiation of the histidine-deficient mutant hi-31 induced a slowly growing reversion to histidine-independence. This formed colonies much smaller than wildtype. By means of transduction the newly created character “small colony” was proved to be heritable. As demonstrated by the following experiments this was due to an independant suppressor-mutation (S-31). After UV-irradiation of hi-31/S-31 a small fraction of cells forming large colonies, revealed growth-characteristics of wildtype. After transduction of small colony type cells by phages raised on wildtype the same large colonies were obtained. Expected to be of genotype hi-31+/S-31, they were used as donor for transduction of hi-31. Both, large colonies (hi-31+/S-31) and small colonies (hi-31/S-31) were isolated, which proved to be stable in further transfers.26 histidin-requiring mutants, belonging to 4 groups, each of them characterised by the same block in histidine synthesis, were transduced with phage raised on hi-31/S-31. None of them exhibited changes of growth characteristics, resulting from the incorporation of the suppressor-gene. Thus the suppressor S-31 turned out to be pseudoallel-specific.This result is considered as evidence that pseudoalleles of the histidine series in Salmonella typhimurium not only are units of recombination but also of function of genetic material. The differences between levels of functions exhibited by units which have been called pseudoalleles by various investigators are discussed in connection with the gene concept.


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