MOLECULAR CONFIGURATION IN SODIUM THYMONUCLEATE
MOLECULAR CONFIGURATION IN SODIUM THYMONUCLEATE
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DOI:
10.1038/171740a0
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发表时间:
1953-01-01
期刊:
影响因子:
64.8
通讯作者:
GOSLING, RG
中科院分区:
文献类型:
--
作者:
FRANKLIN, RE;GOSLING, RG
SODIUM thymonucleate fibres give two distinct types of X-ray diagram. The first corresponds to a crystalline form, structure A, obtained at about 7 5 per cent relative humidity; a study of this is described in detail elsewhere'. At higher humidities a different structure, structure B, showing a lower degree of order, appears and persists over a wide range of ambient humidity. The change from A to B is reversible. The water content of structure B fibres which undergo this reversible change may vary from 40--50 per cent to several hundred per cent of the dry weight. Moreover, some fibres never show structure A, and in these structure B can be obtained with an even lower water content. The X-ray diagram of structure B (see photograph) shows in striking manner the features characteristic of helical structures, first worked out in this laboratory by Stokes (unpublished) and by Crick, Cochran and Vand•. Stokes and Wilkins were the first to propose such structures for nucleic acid as a result of direct studies of nucleic acid fibres, alt, hough a helical structure had been previously suggested by Furberg (thesis, London, 1949) on the basis of X-ray studies of nucleosides and nucleotides. While the X-ray evidence cannot, at present, be taken as direct proof that the structure is helical, other considerations discussed below make the existence of a helical structure highly probable. Structure B is derived from the crystalline structure A when the sodium thymonucleate fibres take up quantities of water in excess of about 40 per cent of their weight. The change is accompanied by an increase of about 30 per cent in the length of tho fibre, and by a substantial re-arrangement of the molecule. It therefore seems reasonable to suppose that in structure B the structural units of sodium thymonucleate (molecules on groups of molecules) are relatively free from the influence of neighbouring