Bacterial degradation of Aroclor 1242 in the mycorrhizosphere soils of zucchini (Cucurbita pepo L.) inoculated with arbuscular mycorrhizal fungi.
Identifieur interne : 001819 ( Main/Corpus ); précédent : 001818; suivant : 001820Bacterial degradation of Aroclor 1242 in the mycorrhizosphere soils of zucchini (Cucurbita pepo L.) inoculated with arbuscular mycorrhizal fungi.
Auteurs : Hua Qin ; Philip C. Brookes ; Jianming Xu ; Youzhi FengSource :
- Environmental science and pollution research international [ 1614-7499 ] ; 2014.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Dioxygenases.
- chemical , metabolism : Aroclors, Dioxygenases, Soil Pollutants.
- metabolism : Actinobacteria, Betaproteobacteria.
- Cucurbita, Glomeromycota, Mycorrhizae, Soil Microbiology.
Abstract
A greenhouse experiment was conducted to investigate the effects of zucchini (Cucurbita pepo L.), inoculated with the arbuscular mycorrhizal (AM) species Acaulospora laevis, Glomus caledonium, and Glomus mosseae, on the soil bacterial community responsible for Aroclor 1242 dissipation. The dissipation rates of Aroclor 1242 and soil bacteria abundance were much higher with the A. laevis and G. mosseae treatments compared to the non-mycorrhizal control. The biphenyl dioxygenase (bphA) and Rhodococcus-like 2,3-dihydroxybiphenyl dioxygenase (bphC) genes were more abundant in AM inoculated soils, suggesting that the bphA and Rhodococcus-like bphC pathways play an important role in Aroclor 1242 dissipation in the mycorrhizosphere. The soil bacterial communities were dominated by classes Betaproteobacteria and Actinobacteria, while the relative proportion of Actinobacteria was significantly (F=2.288, P<0.05) correlated with the PCB congener profile in bulk soil. Our results showed that AM fungi could enhance PCB dissipation by stimulating bph gene abundance and the growth of specific bacterial groups.
DOI: 10.1007/s11356-014-3231-y
PubMed: 24969432
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pubmed:24969432Le document en format XML
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<affiliation><nlm:affiliation>Institute of Soil and Water Resources and Environmental Science, Zhejiang Provincial Key Laboratory of Subtropical Soil and Plant Nutrition, Zhejiang University, Hangzhou, 310058, China.</nlm:affiliation>
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<author><name sortKey="Brookes, Philip C" sort="Brookes, Philip C" uniqKey="Brookes P" first="Philip C" last="Brookes">Philip C. Brookes</name>
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<author><name sortKey="Xu, Jianming" sort="Xu, Jianming" uniqKey="Xu J" first="Jianming" last="Xu">Jianming Xu</name>
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<author><name sortKey="Feng, Youzhi" sort="Feng, Youzhi" uniqKey="Feng Y" first="Youzhi" last="Feng">Youzhi Feng</name>
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<author><name sortKey="Qin, Hua" sort="Qin, Hua" uniqKey="Qin H" first="Hua" last="Qin">Hua Qin</name>
<affiliation><nlm:affiliation>Institute of Soil and Water Resources and Environmental Science, Zhejiang Provincial Key Laboratory of Subtropical Soil and Plant Nutrition, Zhejiang University, Hangzhou, 310058, China.</nlm:affiliation>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Actinobacteria (metabolism)</term>
<term>Aroclors (metabolism)</term>
<term>Betaproteobacteria (metabolism)</term>
<term>Cucurbita (MeSH)</term>
<term>Dioxygenases (genetics)</term>
<term>Dioxygenases (metabolism)</term>
<term>Glomeromycota (MeSH)</term>
<term>Mycorrhizae (MeSH)</term>
<term>Soil Microbiology (MeSH)</term>
<term>Soil Pollutants (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Dioxygenases</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Aroclors</term>
<term>Dioxygenases</term>
<term>Soil Pollutants</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Actinobacteria</term>
<term>Betaproteobacteria</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Cucurbita</term>
<term>Glomeromycota</term>
<term>Mycorrhizae</term>
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<front><div type="abstract" xml:lang="en">A greenhouse experiment was conducted to investigate the effects of zucchini (Cucurbita pepo L.), inoculated with the arbuscular mycorrhizal (AM) species Acaulospora laevis, Glomus caledonium, and Glomus mosseae, on the soil bacterial community responsible for Aroclor 1242 dissipation. The dissipation rates of Aroclor 1242 and soil bacteria abundance were much higher with the A. laevis and G. mosseae treatments compared to the non-mycorrhizal control. The biphenyl dioxygenase (bphA) and Rhodococcus-like 2,3-dihydroxybiphenyl dioxygenase (bphC) genes were more abundant in AM inoculated soils, suggesting that the bphA and Rhodococcus-like bphC pathways play an important role in Aroclor 1242 dissipation in the mycorrhizosphere. The soil bacterial communities were dominated by classes Betaproteobacteria and Actinobacteria, while the relative proportion of Actinobacteria was significantly (F=2.288, P<0.05) correlated with the PCB congener profile in bulk soil. Our results showed that AM fungi could enhance PCB dissipation by stimulating bph gene abundance and the growth of specific bacterial groups.</div>
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<Abstract><AbstractText>A greenhouse experiment was conducted to investigate the effects of zucchini (Cucurbita pepo L.), inoculated with the arbuscular mycorrhizal (AM) species Acaulospora laevis, Glomus caledonium, and Glomus mosseae, on the soil bacterial community responsible for Aroclor 1242 dissipation. The dissipation rates of Aroclor 1242 and soil bacteria abundance were much higher with the A. laevis and G. mosseae treatments compared to the non-mycorrhizal control. The biphenyl dioxygenase (bphA) and Rhodococcus-like 2,3-dihydroxybiphenyl dioxygenase (bphC) genes were more abundant in AM inoculated soils, suggesting that the bphA and Rhodococcus-like bphC pathways play an important role in Aroclor 1242 dissipation in the mycorrhizosphere. The soil bacterial communities were dominated by classes Betaproteobacteria and Actinobacteria, while the relative proportion of Actinobacteria was significantly (F=2.288, P<0.05) correlated with the PCB congener profile in bulk soil. Our results showed that AM fungi could enhance PCB dissipation by stimulating bph gene abundance and the growth of specific bacterial groups.</AbstractText>
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