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Peptidoglycan .Types of Bacterial Cell Walls and their Taxonomic ...

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452 SCHLEIFER AND KANDLER<br />

BACTERIOL REV.<br />

transfer (162a, 432). In particular the different<br />

GC content <strong>of</strong> anaerobic corynebacteria<br />

(47-58%) <strong>and</strong> propionibacteria (66-70%) <strong>and</strong><br />

some physiological features speak against a<br />

close relationship <strong>of</strong> these two groups (408, 410,<br />

411). There is also a rather low level <strong>of</strong> DNA<br />

homology (10-20%) between the anaerobic corynebacteria<br />

<strong>and</strong> classical propionibacteria<br />

(162a). It might be possible that the peptidoglycan<br />

<strong>of</strong> these organisms differs in a similar way<br />

from that <strong>of</strong> the propionibacteria as that <strong>of</strong><br />

Arachnia propionica (vide infra). However,<br />

strains <strong>of</strong> Arachnia propionica show no DNA<br />

homology to either the anaerobic corynebacteria<br />

or the classical propionibacteria (162a).<br />

Variation A4a. Variation A4a which contains<br />

L-Lys in position 3 <strong>of</strong> the peptide subunit was<br />

found in four different peptidoglycan types<br />

(Table 33). Most <strong>of</strong> the strains belong to the<br />

genera Brevibacterium <strong>and</strong> Arthrobacter. The<br />

exceptions are C. manihot <strong>and</strong> Kurthia zopfii.<br />

More physiological <strong>and</strong> genetic data are necessary<br />

to elucidate the relationships within this<br />

group.<br />

-G-M-G-<br />

L- Ala<br />

D-Glu -- Y<br />

NH2<br />

E<br />

L- Lys -L- Thra- L-Ala L-Ala_-(L-Ala)-- D-AIa<br />

L -Ala L- Thr - L-Ala * b<br />

*E L_ Ser L - Thr L- Ala C<br />

D-Ala L-Lys<br />

FIG. 26. Fragments <strong>of</strong> the primary structures <strong>of</strong><br />

threonine-containing peptidoglycans <strong>of</strong> coryneform<br />

organisms (A3a). (a) L-Lys-L-Thr-L-A1a2 3; (b)<br />

L-Lys- L-Ala- L-Thr- L-Ala; (c) L-Lys- L-Ser- L-Thr-<br />

L-Ala.<br />

a)<br />

-G- M-G-<br />

L<br />

L- Ala<br />

D- Glu -. Gly<br />

1-Y r------- -____<br />

LL- Dpm Gly.- Gly_- Gly .- D- Ala<br />

D-Ala LL- Dpm<br />

t<br />

Variation A45B. This variation has only been<br />

found in the genus <strong>Cell</strong>ulomonas (Table 33).<br />

This genus is characterized by the ability to<br />

decompose cellulose <strong>and</strong> to produce acid from<br />

carbohydrates. These features together with the<br />

distinct peptidoglycan types justify the genus<br />

<strong>Cell</strong>ulomonas despite the objections <strong>of</strong> Jensen<br />

(161). With the exception <strong>of</strong> C. flavigena which<br />

contains the L-Orn-D-Asp type peptidoglycan,<br />

all the other species contain the L-Orn-D-Glu<br />

type (F. Fiedler, <strong>and</strong> 0. K<strong>and</strong>ler, Arch. Microbiol.,<br />

in press). (The amino acid composition <strong>of</strong><br />

cell walls <strong>of</strong> C. fimi, C. gelida ATCC 488, C.<br />

flavigena ATCC 482, <strong>and</strong> C. biazotea ATCC 486<br />

were qualitatively studied by Sukapure et al.<br />

(372). Their results were not in agreement with<br />

our findings. In the case <strong>of</strong> C. fimi <strong>and</strong> C. gelida<br />

ATCC 488, they found both Orn <strong>and</strong> Lys; in the<br />

case <strong>of</strong> C. flavigena ATCC 482 <strong>and</strong> C. biazotea<br />

ATCC 486, they did not find any diamino acid.<br />

We have obtained a subculture <strong>of</strong> the latter<br />

strain from M. Lechevalier, New Brunswick,<br />

<strong>and</strong> confirmed the presence both <strong>of</strong> Asp <strong>and</strong> <strong>of</strong><br />

L-OM in the cell walls. Physiological studies,<br />

however, have shown that this strain behaves as<br />

a typical C. flavigena. To clarify this discrepancy,<br />

a new subculture <strong>of</strong> C. biazotea ATCC<br />

486 was obtained from the American Type<br />

Culture Collection. The determination <strong>of</strong> the<br />

peptidoglycan type corroborated our previous<br />

findings that C. biazotea ATCC 486 contains<br />

a L-Orn-D-Glu type.)<br />

Variation A4,y. <strong>Peptidoglycan</strong>s <strong>of</strong> variation<br />

A4y were only detected in some coryneform<br />

bacteria <strong>and</strong> a few micrococci <strong>of</strong> doubtful taxonomic<br />

position (Table 33; 39). The occurrence<br />

<strong>of</strong> such a unique peptidoglycan type among a<br />

small group <strong>of</strong> strains makes a relationship<br />

between these strains quite likely. But further<br />

b)<br />

-G-M-G-<br />

1<br />

L-Ala<br />

D-Glu<br />

IY r - _<br />

m-Dpm -(i)' D-Asp24D-Ala<br />

L-<br />

---------J I<br />

D-Ala m-Dpm<br />

t<br />

FIG. 27. Fragments <strong>of</strong> the primary structures <strong>of</strong> Dpm-containing peptidoglycans (A3-y <strong>and</strong> A4y) <strong>of</strong><br />

coryneform organisms. (a) L, L-Dpm-Gly3, A. tumescens ATCC 9647; (b) m-Dpm-D-Asp2, A. duodecadis<br />

ATCC 13347.<br />

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