Literature DB >> 11776

Isolation, characterization and oxygen equilibrium of an extracellular haemoglobin from Eunice aphroditois (Passas).

J V Bannister, W H Bannister, A Anastasi.   

Abstract

The extracellular haemoglobin from the polychaeta,Eunice aphroditois, existed as a mixture of a heavy major component (so20, w = 56.96 +/- 0.125) and a light minor component (so20, w = 10.00 +/- 0.13S), the latter probably being a dissociation product of the former. The molecular weight of the purified heavier component, as detetermined by sedimentation equilibrium, was 3.44 x 10(6) +/- 0.04x10(6). The molecule had the electron-microscopic appearance typical of annelid haemoglobins, consisting of a stack of two hexagonal plates, with dimensions 26.32 +/- 0.27 nm across the flats of the hexagon, height of stack 17.86 +/- 0.34 nm. The sugar composition is reported, and the isoelectric point was approx. pH7.8. The haem content was 2.31 +/- 0.01%, corresponding to a minimal mol.wt. of 26700. Detergent/gel electrophoresis revealed the presence of at least four bands with molecular weights in the range 14600-31000. Five N-terminal amino acids were found. In addition to the 10S component, which co-existed with the 57S component at all pH values in the range 4.0-10.6, at low pH values (less than pH.5.0) A 16S and a 1.9 S component were found. The absorption and circular-dichroic spectra are reported, and the alpha-helical content, calculated from the ellipticity at 222 nm, was about 40%. The molecule bound O2 co-operatively with a maximum value of the Hill coefficient, h, of 3.9. Over the pH range 7.0-8.0 there was a positive Bohr effect.

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Year:  1976        PMID: 11776      PMCID: PMC1164035          DOI: 10.1042/bj1590035

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  20 in total

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6.  The extracellular haemoglobin of Eunice aphroditois (Pallas).

Authors:  E J Wood; A Anastasi; W H Bannister; J V Bannister
Journal:  Biochem Soc Trans       Date:  1976       Impact factor: 5.407

7.  Subunit homology in invertebrate hemoglobins: a primitive heme binding chain?

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10.  SPECTRA OF DEOXYGENATED HEMOGLOBIN IN THE SORET REGION.

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  4 in total

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Journal:  Biochem J       Date:  1978-06-01       Impact factor: 3.857

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4.  The structure of Artemia sp. haemoglobin. Cleavage of the native molecules into functional units by limited subtilisin digestion.

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  4 in total

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