It can produce blueish-green pigment in nutrient broth. Can utilize gelatin. Can produce H2S in SIM medium, urease positive, citrate and catalase positive. And it is also a phosphate solubilising bacteria, can produce IAA.
I am surprised that so many suggested elaborate test when you can get for much less effort and money / time the definite answer using 16S rRNA sequence (Cost of sequence is about US $ 5 -29 , depending on the service, If the sequence is between two species you can do --based on Bergey's-- very few differentiating tests to nail it down. Don't forget you also could have a novel taxa and you don't find that out by just doing the suggested test.. Don't think in a box. -
I would vote for Pseudomonas as well, in particular, P. aeruginosa. Are cells rod-shaped and motile (I assume you've looked at the culture under the microscope?)
Pseudomonas aeruginosa or Pseudomonas fluorescens, depending on biochemical profile. Knowing where it was isolated from would help. Burkholderia cepacia is a less likely hypothesis.
Where was it isolated from?Infection/ enviromental sample? That information might greatly contribute to the right identification. As aforementioned, I also strongly recommend you DNA extraction and further sequencing of 16S rDNA amplicons. Identification based on sequencing helps to avoid misleading results associated with variable expression of some phenotypic traits depending on strain or cullture condition e.g. carbohydrate fermentation or other metabolic capabilities. Good luck!
yes i agree the last opinions especially with Mike Mitzel because this the right way to classify any strain. also you have to do one PCR run using the specific primer. Hence you will be sure that you have pseudomonase strain or what.....good luck
ya this may be Pseudomonas sp if you want to confirm check in pseudomonas agar if it grows it wll confirm as Pseudomonas while checking see the fluoresence if it shows fluorescense it is confirm Pseudomonas sp
I suggest you send your plates to a contract lab for microbial identification, you may need to know the genetic aspects of all microorganisms identify or you can do it yourself by using biomerieux API kits or Remel.
You can get the genus by doing 16srDNA sequencing, then if you submit the sequence in NCBI blastn databases, it will give you the possible matches of the genus. like this by biochemical characterization you can't be confirmed 100%.
I also agree that 16S rDNA sequencing can solve your problem.The Pseudomonas genus is one of the most diverse genera. It is a bit tricky to identify Pseudomonas species based on biochemical tests and cultivation on different media. If you have possibility try to do the 16S rDNA sequencing (at least the parital sequencing).
One thing I can tell you that P. aeruginosa is urease negative...so your culture might be some other species of Pseudomonas..You should check the family pseudomonadaceae in Bergey's Manual of systematic bacteriology and match your results of biochemical tests..
Probably it is a specie of Genus pseudomona. Why don´t you test oxidase? If it is oxidase negative, then it is most likely to be Proteus and you can test for swarming in nutrient agar.
Mr.Dipak Paul first send the details about colony morphology, source of bacterium, gram's feature, oxidase, if gram negative, whether you have checked or confirmed with 3% KOH, then all biochemical tests performed.
What is the Gram reaction and what is the shape of the bacteria when seen under the microscope? Not all green pigment producing bacteria are Pseudomonas sp
Dipak you just go for FAME analysis once you got the result you just compare with 16S rDNA sequencing data it probably will give the better result of your bacteria.........
This bacterium is certainly Pseudomonas,Melt gelatin tests, the sugar trehalose, growth at temperatures of 41 and 4 ° C. is major indexes for Separation of the Pseudomonas species, But I think it is Pseudomonas aeruginosa.
you need to follow a systematic approach to the identification, colony morphology, microscopic morphology, gram stain, primary/secondary biochemical tests. Then followed by the specific genus/species tests. This would be the standard approach that all science student are shown in year one. Use a good book, eg Bergies Manual to perform the identification. Unless you do this your isolate could be anything.
I also think you should use a systemaytic approach for the identification, or if you can you could go for a 16S seqeunce whcih gives you really good informations. But I think that this bacterium is close related to some Pseudomonas species. The coloration could be due to phenazine production, check this paper http://www.nature.com/nchembio/journal/v2/n2/abs/nchembio764.html
as per your biochemical test it may be Pseudomonas..better your try to sub culture it on Kings B agar which is selective medium for Pseudomonas. and try with Cetramide agar too..for better confirmation 16S rRNA sequencing is best option
Hi Dipak, thanks for posting this question. Your bug appears to be a Pseudomonas to me also.... though a confirmatory test would be better. Depending on your time and available funds you can try to identify your bacterium. If you have funds for a 16S rRNA analysis, please go ahead and do that (you can reach the IISER in kalyani; IICB/ICGEB/IMTECH/CCMB/NCL/NIO/IITKGP/TIFR/ and many more institutes in India itself who can do it for you in less than 3k INR). If you have time but lack of funds, please grab the Bible for microbiology (Bergey's manual ), carry out some (may be lots too) biochemical tests, and you should be done with the identification unless you have a new bug that would be very difficult to funnel out from those tests and charts... Good luck...:-)
I am surprised that so many suggested elaborate test when you can get for much less effort and money / time the definite answer using 16S rRNA sequence (Cost of sequence is about US $ 5 -29 , depending on the service, If the sequence is between two species you can do --based on Bergey's-- very few differentiating tests to nail it down. Don't forget you also could have a novel taxa and you don't find that out by just doing the suggested test.. Don't think in a box. -
It may be Pseudomonas.fluorescence .Because it got the ability to produce both pyoverdin and pyocyanin ,And this microbes got little effect on phosphorus soliubilization around (0.6-0.8 ) PPM. For more details go for inhibition tests as it is effective against rice sheath rot disease .....All the best