Biosynthesis cellulose synthase genes

Ranik M. and Myburg A. A. 2006. Six new cellulose synthase genes from Eucalyptus are associated with primary and secondary cell wall biosynthesis. Tree Physiology 26 545-556. 

The parallels among chitin, cellulose, and HA structures, all being j3 -chains of hexose polymers are reflected in the striking similarity in sequence between the HAS from vertebrates, cellulose synthases from plants, and chitin synthases from fungi. A primordial ancestral gene must have existed from which all of these enzymes evolved that are involved in the biosynthesis of all polymers that contain -glycoside linkages, an ancient j3-polysaccharide synthase. 

Available evidence supports a common ancestry for all cellulose synthases. These enzymes appear to have been a bacterial invention acquired by various eukaryotes via multiple lateral gene transfers. However, the proteins associated with regulation of cellulose biosynthesis and polymer crystallization seem to have evolved independently. Sequence divergence of eukaryotic cellulose synthases and the presence of multiple gene clusters associated with bacterial cellulose synthases are discussed in relation to the possible evolutionary pathways of cellulose biosynthesis. 

The proliferation of complete genome sequences in public databases provides an additional means to track the evolution of cellulose in bacteria. Conservation of operons and/or gene clusters (synteny) can be used to trace not only the history of cellulose synthase, but also its associated proteins. The existence of a few these gene clusters has been well documented. In the sections below, I would like to give a brief review of the known gene organizations and introduce two novel ones which may be linked to the eukaryotic acquisition of cellulose biosynthesis. 

Although all proteins encoded by Group I and II gene clusters are necessary for wild-type cellulose biosynthesis, only cellulose synthases have a known function. ... 

Current data suggest that cellulose biosynthesis is a bacterial invention and that eukaryotes acquired the process via multiple lateral gene transfers. Bacteria and eukaryota have independently evolved regulatory mechanisms and molecular structures to utilize the p-1,4-homopolymer synthesized by the catalytic activity of homologous cellulose synthase enzymes. The differences in accessory enzymes probably reflect not only convergent evolution to produce a cellulose I crystalline allomorph, but also inventions of alternative products such as cellulose II, noncrystalline cellulose, or nematic ordered cellulose. 

A characteristic feature of the SuSy isoforms is a conserved phosphorylated serine residue near the N-terminus [8-10]. In-vivo studies have demonstrated that phosphorylation and dephosphorylation direct the distribution of SuSy isoforms in the plant cell [10-12]. The soluble phosphorylated SuSy interacts with the actin cytoskeleton in the cytoplasm [13], and the dephosphorylated SuSy isoforms are targeted to the cell membrane to form complexes with other enzymes, e.g., glucan synthase, catalyzing cellulose biosynthesis from sucrose [4, 10, 14]. In this respect, recent studies on the dephosphorylated enzymes by cloning and expression of SMS genes in E. coli have shown differences in some biochemical features when compared to the enzymes isolated from the corresponding plant material. Recom-... 

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