C. Peter Wolk

C. Peter Wolk

Professor Emeritus
Department of Plant Biology

  Office: (517) 353-2049

  wolk@msu.edu

    MSU-DOE Plant Research Laboratory
     Michigan State University
     Plant Biology Laboratories
     612 Wilson Road, Room S-252
     East Lansing, MI 48824


Publications

PubMed Search


Research: Developmental Mechanisms in Filamentous Cyanobacteria

The filamentous cyanobacterium Anabaena provides models of the short-range intercellular interactions that control development in many organisms. When Anabaena grows in the presence of abundant fixed nitrogen, all of its cells appear to be of the same type, referred to as a vegetative cell. When nitrogen becomes limiting, 5 to 10% of the cells differentiate, at semi-regular intervals along the filaments, into nitrogen-fixing cells called heterocysts. In some species, yet a third type of cell, the akinete (or spore), can differentiate from vegetative cells positioned adjacent to heterocysts. Pre-existing heterocysts inhibit nearby cells from differentiating into heterocysts and (in some species) induce nearby cells to become akinetes. We wish to know how they do so.

 

Figure 1. Filaments of Anabaena cylindrica. Heterocysts (H) are nitrogen-fixing cells. Enlarged spores (S), a.k.a. akinetes, here still immature, form by differentiation of vegetative cells adjacent to heterocysts, and can germinate after exposure to harsh conditions. The remaining vegetative cells of the filaments photosynthesize and grow.

 

We devised genetic methodology to facilitate molecular analysis of the development of Anabaena. If restriction by cyanobacterial endonucleases is avoided, DNA can be transferred with high efficiency from Escherichia coli to Anabaena by conjugation of bacterial plasmids. Mutations can thereupon be generated and complemented, and reporter genes can be used to visualize the cells in which promoters are active and, within cells, where particular proteins are localized. The genomes of numerous strains have been sequenced and transposons active in Anabaena are available.

Now emeritus, I pursue the genetics of Anabaena development in collaboration with others, with an emphasis on novel roles of transposons that may enhance understanding of regulation of photosynthesis and of akinete formation. I continue to seek an understanding of why it is that Anabaena PCC 7120, a model for study of heterocyst formation, lacks akinete formation, motility, and synthesis of gas vacuoles.