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Fake Banner
By Hatice Cullingford | November 17th 2009 02:53 PM | 4 comments | Print | E-mail | Track Comments
About Hatice

Welcome to my universe.. where there is Peace University.

As Fine Scientist, PhD, I write about my interest in various fields, from...

View Hatice's Profile
Bacteria are abundant in soil, water, and air as well as in the depths of the Earth's crust, organic matter, and live animals or plants. They are also abundantly social -- among themselves and with others. Not only do they interact with each other but also with their host. Bacillus subtilis and Streptomyces coelicolor are two examples from daily life. The former would be involved with the ropiness of spoiled bread. But the well-known Streptomyces produce the soil's earthy aroma and flavor and the majority of today's antibiotics.

Pieter Dorrestein and his team -- Yu-Liang Yang and Yuquan Xu -- at the University of California, San Diego (UCSD) have colloraborated with Paul Straight of Texas A&M University (TAMU) on a new approach to visualize bacteria communicate with one another. Translating metabolic exchange with imaging mass spectrometry [IMS] describes their research in Nature Chemical Biology: "We have developed a mass spectrometry–based method that enables us to visualize both the spatial and temporal production of numerous metabolites from a single bacterial species and to observe the effects of multiple microbial signals in an interspecies interaction."  


/images/uploads/2009/11/5/dorrestein.jpg 


Pieter Dorrestein: Assistant Professor, the Skaggs School of Pharmacy and Pharmaceutical Sciences and the Departments of Pharmacology,
Chemistry, and Biochemistry at UCSD and member, Center for Marine Biotechnology and Biomedicine at the Scripps Institution of Oceanography 


Bacteria produce many small molecules as both communication and warfare with other bacteria, but until new imaging techniques were recently developed, scientists only saw a small fraction of them, according to Dr. Paul Straight, Texas AgriLife Research scientist. In the center of this graphic is a photograph of two colonies of bacteria. On either side are images in false-color made with a mass spectrometer showing some of the molecules that are produced. At the top of the graphic are representations of the molecules. (Graphic by Jeramie Watrous, University of California, San Diego)

Left: Colonies of Bacillus subtilis grown on a culture dish. (Credit: Wkipedia)

Right: Graphic by Jeramie Watrous (UCSD). Two colonies of bacteria and their false-color images.
Bottom: Colonies of Streptomyces coelicolor, secreting blue actinorhodin antibiotic. (Credit: John Innes Centre)

In the graphic above (right) you see at the center a photograph of two colonies of bacteria and on either side their false-color images that were made with a mass spectrometer. Some of the bacterial products are also shown at the top along with molecular formulas.

The UCSD/TAMU team told us how to study an interaction between two species of bacteria in a new way and provided direct evidence that Bacillus subtilis silences the defensive arsenal of Streptomyces coelicolor. Their approach relies on adaptation of MALDI-TOF imaging technology to observe secondary metabolite production from bacteria cultivated on a thin layer of agar on top of the MALDI plate.




The essential steps in measuring with a mass spectrometer

Credit: Wikipedia

Bacteria interactions are now expressible in terms of molecules that can be seen in laboratory conditions for the first time since R. Muller named Streptomyces coelicolor as Streptothrix coelicolor about a century ago. Below is a picture of bacteria talking. The optical photograph of the colonies appears at the top. Red and green colors indicate the small molecules surfactin and SapB, respectively. We see timecourse data on surfactin inhibiting S. coelicolor's SapB production -- and aerial hyphae formation 


/images/uploads/2009/11/5/bacteria.jpg 
Seeing bacteria talk - the colors are the molecules used by bacteria
to communicate. Red, surfactin. Green, SapB. (UCSD)


Dorrestein et al. used IMS to observe chemical interactions between Bacillus subtilis and Streptomyces coelicolor to validate their method. IMS gave "accurate identification of small-molecule metabolites based on their mass with sufficient sensitivity to detect ions across the entire grid." A new era began with this experimental development in understanding complex bacterial interactions.



Comments

why is this published in "immunology"? this has nothing to do with the subject.

Hatice Cullingford's picture
Hi Anomymous. Thanks for your comment and question. My decision involved many topics such as pharmacology, microbiology, genetics and molecular biology, etc. at Scientific Blogging (SB). Considering immunology involves many bodies such as human and physical/chemical/physiological characteristics.. etc., and many mysteries at this time I chose it.

Because I see this research powerful in immunology says volumes about my excitement over the results. Let me ask you, where would you place it?

Immunology is under Life Sciences at SB. Pharmacology under Medicine. Thus I thought of covering both life sciences (scroll) and medicine (hence pharmacology). Pharmacology appeared 'limiting' to me under SB topics.

Let me hear from you. I appreciate your interest.

this is an article about soil bacteria. if you saw a microbiology heading, that would be the absolute most appropriate place to put it, and I don't know why you didn't.

"powerful in immunology?" this has NOTHING to do with immunology. zip. zero. zilch.

immunology is a very narrow field of study -- the immune system. yes it involves genetics and molecular biology, etc. but it is more narrow than these topics, and you seem to think it is less so. soil bacteria don't come into play here, unless the article is specifcally talking about the immune system fighting off these soil bacs.

And for the record, this has nothing to do with pharmacology either. Just microbiology.

Steve Davis's picture
Some people just get out of the wrong side of the bed, Hatice. An interesting article, thank you.

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