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Volume 271,
Number 3,
Issue of January 19, 1996 pp. 1475-1479
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Conversion of
Chlorophyll b to Chlorophyll a via 7-Hydroxymethyl
Chlorophyll
(Received for publication, September 18, 1995; and in revised form, November 6, 1995)
Hisashi
Ito ,
Tatsuyuki
Ohtsuka ,
Ayumi
Tanaka
Chlorophyll b is synthesized from chlorophyll a by the oxidation of the methyl group on the ring B of the
tetrapyrrole ring to the formyl group. Previously, we reported that
chlorophyllide b could be converted to chlorophyll a in isolated cucumber etioplasts indicating the conversion of
chlorophyll b to chlorophyll a. To identify the
intermediate molecule, we used barley etioplasts instead of cucumber.
Chlorophyll a and an additional pigment were found after
incubation of chlorophyllide b with isolated barley
etioplasts. The pigment has the same retention time and absorption
spectrum as 7-hydroxymethyl chlorophyll, which has the hydroxymethyl
group on ring B instead of the formyl group of chlorophyll b.
Authentic 7-hydroxymethyl chlorophyll was prepared by reduction of
chlorophyll b by NaBH . Chlorophyll a accumulated during the incubation of 7-hydroxymethyl
chlorophyllide with etioplasts. These findings indicate that
chlorophyll b is converted to chlorophyll a via
7-hydroxymethyl chlorophyll. Chlorophyll b and 7-hydroxymethyl
chlorophyll accumulated within a short period of incubation of
chlorophyllide b with etioplasts. However, chlorophyll a accumulated with a concomitant decrease of chlorophyll b and 7-hydroxymethyl chlorophyll. These observations also suggest
that chlorophyll b is converted to 7-hydroxymethyl chlorophyll
and then to chlorophyll a. Both steps required ATP.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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