Minimal transcriptional regulation of horizontally transferred photosynthesis genes in phototrophic bacterium Gemmatimonas phototrophica

被引:1
作者
Kopejtka, Karel [1 ]
Tomasch, Juergen [1 ]
Shivaramu, Sahana [1 ]
Saini, Mohit Kumar [1 ]
Kaftan, David [1 ]
Koblizek, Michal [1 ]
机构
[1] Czech Acad Sci, Lab Anoxygen Phototrophs, Inst Microbiol, Trebon, Czech Republic
关键词
Gemmatimonadota; anoxygenic photosynthesis; bacteriochlorophyll; horizontal gene transfer; transcriptomics; AEROBIC ANOXYGENIC PHOTOTROPHS; BACTERIOCHLOROPHYLL; GROWTH; LIGHT; EXPRESSION; STATE;
D O I
10.1128/msystems.00706-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The first phototrophic member of the bacterial phylum Gemmatimonadota, Gemmatimonas phototrophica AP64(T), received all its photosynthesis genes via distant horizontal gene transfer from a purple bacterium. Here, we investigated how these acquired genes, which are tightly controlled by oxygen and light in the ancestor, are integrated into the regulatory system of its new host. G. phototrophica grew well under aerobic and semiaerobic conditions, with almost no difference in gene expression. Under aerobic conditions, the growth of G. phototrophica was optimal at 80 mu mol photon m(-2) s(-1), while higher light intensities had an inhibitory effect. The transcriptome showed only a minimal response to the dark-light shift at optimal light intensity, while the exposure to a higher light intensity (200 mu mol photon m(-2) s(-1)) induced already stronger but still transient changes in gene expression. Interestingly, a singlet oxygen defense was not activated under any conditions tested. Our results indicate that G. phototrophica possesses neither the oxygen-dependent repression of photosynthesis genes known from purple bacteria nor the light-dependent repression described in aerobic anoxygenic phototrophs. Instead, G. phototrophica has evolved as a low-light species preferring reduced oxygen concentrations. Under these conditions, the bacterium can safely employ its photoheterotrophic metabolism without the need for complex regulatory mechanisms. IMPORTANCE Horizontal gene transfer is one of the main mechanisms by which bacteria acquire new genes. However, it represents only the first step as the transferred genes have also to be functionally and regulatory integrated into the recipient's cellular machinery. Gemmatimonas phototrophica, a member of bacterial phylum Gemmatimonadota, acquired its photosynthesis genes via distant horizontal gene transfer from a purple bacterium. Thus, it represents a unique natural experiment, in which the entire package of photosynthesis genes was transplanted into a distant host. We show that G. phototrophica lacks the regulation of photosynthesis gene expressions in response to oxygen concentration and light intensity that are common in purple bacteria. This restricts its growth to low-light habitats with reduced oxygen. Understanding the regulation of horizontally transferred genes is important not only for microbial evolution but also for synthetic biology and the engineering of novel organisms, as these rely on the successful integration of foreign genes.
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页数:14
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共 53 条
[1]  
Androga DD., 2012, PHOTOFERMENTATIVE HY
[2]   Transcriptome dynamics during the transition from anaerobic photosynthesis to aerobic respiration in Rhodobacter sphaeroides 2.4.1 [J].
Arai, Hiroyuki ;
Roh, Jung Hyeob ;
Kaplan, Samuel .
JOURNAL OF BACTERIOLOGY, 2008, 190 (01) :286-299
[3]   Horizontal gene transfer and adaptive evolution in bacteria [J].
Arnold, Brian J. ;
Huang, I-Ting ;
Hanage, William P. .
NATURE REVIEWS MICROBIOLOGY, 2022, 20 (04) :206-218
[4]   Anoxygenic photosynthesis and photooxidative stress: a particular challenge for Roseobacter [J].
Berghoff, Bork Ansgar ;
Glaeser, Jens ;
Nuss, Aaron Mischa ;
Zobawa, Monica ;
Lottspeich, Friedrich ;
Klug, Gabriele .
ENVIRONMENTAL MICROBIOLOGY, 2011, 13 (03) :775-791
[5]   Fixation of CO2 using the ethylmalonyl-CoA pathway in the photoheterotrophic marine bacterium Dinoroseobacter shibae [J].
Bill, Nelli ;
Tomasch, Juergen ;
Riemer, Alexander ;
Mueller, Katrin ;
Kleist, Sarah ;
Schmidt-Hohagen, Kerstin ;
Wagner-Doebler, Irene ;
Schomburg, Dietmar .
ENVIRONMENTAL MICROBIOLOGY, 2017, 19 (07) :2645-2660
[6]   BACTERIOCHLOROPHYLL ALPHA-TRIPLET STATE AND ITS INTERACTIONS WITH BACTERIAL CAROTENOIDS AND OXYGEN [J].
BORLAND, CF ;
COGDELL, RJ ;
LAND, EJ ;
TRUSCOTT, TG .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1989, 3 (02) :237-245
[7]   Early anaerobic metabolisms [J].
Canfield, Don E. ;
Rosing, Minik T. ;
Bjerrum, Christian .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2006, 361 (1474) :1819-1834
[8]   PufQ regulates porphyrin flux at the haem/bacteriochlorophyll branchpoint of tetrapyrrole biosynthesis via interactions with ferrochelatase [J].
Chidgey, Jack W. ;
Jackson, Philip J. ;
Dickman, Mark J. ;
Hunter, C. Neil .
MOLECULAR MICROBIOLOGY, 2017, 106 (06) :961-975
[9]   Unique double concentric ring organization of light harvesting complexes in Gemmatimonas phototrophica [J].
Dachev, Marko ;
Bina, David ;
Sobotka, Roman ;
Moravcova, Lenka ;
Gardian, Zdenko ;
Kaftan, David ;
Slouf, Vaclav ;
Fuciman, Marcel ;
Polivka, Tomas ;
Koblizek, Michal .
PLOS BIOLOGY, 2017, 15 (12)
[10]   Oxygen Reductases in Alphaproteobacterial Genomes: Physiological Evolution From Low to High Oxygen Environments [J].
Degli Esposti, Mauro ;
Mentel, Marek ;
Martin, William ;
Sousa, Filipa L. .
FRONTIERS IN MICROBIOLOGY, 2019, 10