Genetic and physical mapping of the Rhodobacter sphaeroides photosynthetic gene cluster from R-prime pWS2

Yong Qiang Wu, Barbara J. MacGregor, Timothy J. Donohue, Samuel Kaplan, Bill Yen

Research output: Contribution to journalArticlepeer-review

6 Scopus citations


Plasmid pWS2 is an R68.45 chimera originally isolated as an R-prime which complemented the Rhodobacter sphaeroides bch-420 allele. Our experiments have shown that pWS2 is also able to complement a wide range of R. sphaeroides pigment and photosynthetic mutants employing nitrosoquanidine, transposon or insertion-generated mutations effecting puhA, puc, puf, cycA, bch, and crt genes. A combination of orthogonal-field-alternation gel electrophoresis, transverse alternating field gel electrophoresis, and conventional electrophoresis have been used to estimate the size of pWS2 at ∼-168.3 ± 3.5 kb. A restriction map of the ∼-109 kb of R. sphaeroides insert DNA was generated by partial and complete restriction endonuclease digestion coupled with Southern hybridization analysis using either gene-specific or junction fragment probes. Genes encoding bacteriochlorophyll (Bchl)-binding proteins (pufBALMX, pucBA, and puhA), cytochrome c2 (cycA), and enzymes involved in Bchl (bch) and carotenoid (crt) biosynthesis have been shown to reside within a contiguous 53-kb region of the R. sphaeroides DNA present on pWS2. The puf operon lies at one end of the 53-kb segment, while the genes puhA, cycA, and pucBA, the latter two of which are located within ∼-12.0 kb of each other, define the other end of this 53-kb region. The genetic and physical mapping data provided in this paper are discussed in terms of the similarities and differences in the organization of the photosynthetic gene cluster between R. sphaeroides and other photosynthetic bacteria as well as highlighting the use of pWS2 in studies of photosynthetic gene structure and function.

Original languageEnglish (US)
Pages (from-to)163-176
Number of pages14
Issue number3
StatePublished - May 1991

Bibliographical note

Funding Information:
This work was supported by Grant GM3 1667 to SK. T.J.D. derived partial support for this work from the Department of Agriculture Hatch Project WIS 3028 and Public Health Service Grant GM37509. B.J.M. was supported by the Public Health Service Cellular and Molecular Biology Predoctoral Training Grant GM072 15 to the University of Wisconsin from the National Institutes of Health.

Copyright 2014 Elsevier B.V., All rights reserved.


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