A special advantage has been conferred upon Chlorella cells as tools in bio
technology when viruses (Phycodnaviridae) infecting Chlorella cells were di
scovered and isolated. The viruses are large icosahedral particles (150-200
nm in diameter), containing a giant, 330-380 kbp long, linear dsDNA genome
. Recently, the nucleotide sequence of the 330,740-bp genome of PBCV-1, the
prototype virus of Phycodnaviridae, was determined, and up to 702 open rea
ding frames (ORFs) were identified along the genome. The possible genes pre
sent include those encoding a variety of enzymes involved in the modificati
on of DNA, RNA, protein and polysaccharides as well as those involved in th
e metabolism of sugars, amino acids, lipids, nucleotides and nucleosides. M
any of these genes are actually expressed during viral infection, with func
tional enzymes detected in the host cytoplasm or incorporated into the viri
on. The successful utilization of these viral enzymes as various DNA restri
ction and modification enzymes (Cvi enzymes) that are now commercially avai
lable is well documented. Also noteworthy are virion-associated chitinase a
nd chitosanase activities that have potentially important applications in t
he recycling of natural resources. The virions of Chlorella viruses contain
more than 50 different structural proteins, ranging in size from 10 to 200
kDa. Some of these proteins may be replaced with useful foreign proteins u
sing recombinant DNA technology. The proteins of interest can be recovered
easily from the viral particles, and collected by centrifugation after comp
lete lysis of the host Chlorella cells.