Affiliation:
1. Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01002
Abstract
A strain of
Spirochaeta aurantia
was isolated from mud by a procedure involving migration of the organisms through cellulose ester filter discs (0.3-μm pore diameter) onto the surface of culture plates. The helical cells measured 0.3 by 10 to 20 μm during exponential growth. Electron microscopy showed the presence of two subterminally inserted axial fibrils partially overlapping in a 1-2-1 arrangement. An outer envelope, exhibiting a polygonal substructure, was observed. The spirochete grew either aerobically or anaerobically, with aerobic yields of 9.8 × 10
8
cells per ml and anaerobic yields of 3.0 × 10
8
cells per ml. The organism used carbohydrates, but not amino acids, as energy sources. Amino acids served as sole nitrogen sources, whereas inorganic ammonium salts did not. The presence of biotin and thiamine in the medium was required for growth. Growing cells fermented maltose mainly to carbon dioxide, hydrogen, ethyl alcohol, and acetic acid. Small amounts of formic and lactic acids, acetoin, and diacetyl were produced. Cells of
S. aurantia
growing aerobically produced a yellow-orange pigment. Chemical analysis indicated that the pigment was carotenoid in nature, its main component being lycopene or a similar compound.
S. aurantia
is not closely related to the leptospires, since it lacks both the hemolytic antigen and the hooked ends typical of the latter organisms. Furthermore, the guanine plus cytosine content in the deoxyribonucleic acid of
S. aurantia
(66.8 moles%) differs drastically from that of leptospires.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
55 articles.
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