Microbial Resistance Mechanisms to the Antibiotic and Phytotoxin Fusaric Acid

Fusaric acid (FA) produced by Fusarium oxysporum plays an important role in disease development in plants, including cotton. This non-specific toxin also has antibiotic effects on microorganisms. Thus, one expects a potential pool of diverse detoxification mechanisms of FA in nature. Bacteria and fungi from soils infested with Fusarium and from laboratory sources were evaluated for their ability to grow in the presence of FA and to alter the structure of FA into less toxic compounds.None of the bacterial strains were able to chemically modify FA. Highly FA resistant strains were found only in Gram-negative bacteria, mainly in the genus of Pseudomonas. The FA resistance of the Gram-negative bacteria was positively correlated with the number of predicted genes for FA efflux pumps present in the genome. Phylogenetic analysis of predicted FA resistance proteins (FUSC, an inner membrane transporter component of the efflux pump) revealed that FUSC proteins having high sequence identities with the functionally characterized FA resistance protein FusC or Fdt might be the major contributors of FA resistance. In contrast, most fungi converted FA to less toxic compounds regardless of the level of FA resistance they exhibited. Five derivatives were detected, and the detoxification of FA involved either oxidative reactions on the butyl side chain or reductive reactions on the carboxylic acid group. The production of these metabolites from widely different phyla indicates that resistance to FA by altering its structure is highly conserved. A few FA resistant saprophytic or biocontrol strains of fungi were incapable of altering FA, indicating a possible involvement of efflux transporters. Deployment of both efflux and derivatization mechanisms may be a common feature of fungal FA resistance

Glandless seed and glanded plant research in cotton. A review

Recently the world has been entangled by insufficient food such as the lack of rice which threatens the safety of world food and affect sustainable development of the world economy, resulting in rising of food price. To address this issue, cotton appears as a possible source of both fiber and food. The research in recent years indeed showed bright prospects for this expectation. However, gossypol stored in the glands of cotton is toxic to nonruminant animals and humans, which wastes large amounts of cottonseed protein that could potentially provide the annual protein requirements for half a billion people. Gossypium species are characterized by their lysigenous glands containing terpenoid aldehydes, important secondary phytoalexins consisting mainly of gossypol, which constitute one of the important plant’s defense system against pests and diseases. The best approach to address this issue is to create glandless seed and glanded plant cotton. A breakthrough in this field would realise the fulfilment of making cotton both a fiber and a food crop, which would be a feat of great magnitude for sustainable development of agriculture. Research on the relationship between glands and their secondary inclusions at the molecular level would be one approach for genetic engineering to control the glands and gossypol content. In this article, we review recent progress on glands and gossypol content for diverse gland types in Gossypium species, inheritance of glands and gossypol content, traditional breeding of glandless seeds and glanded plant cotton, the terpenoid aldehyde biosynthesis pathway, molecular cloning of the related genes, the strategy for genetic engineering, and future prospects

Microbial Resistance Mechanisms to the Antibiotic and Phytotoxin Fusaric Acid

Fusaric acid (FA) produced by Fusarium oxysporum plays an important role in disease development in plants, including cotton. This non-specific toxin also has antibiotic effects on microorganisms. Thus, one expects a potential pool of diverse detoxification mechanisms of FA in nature. Bacteria and fungi from soils infested with Fusarium and from laboratory sources were evaluated for their ability to grow in the presence of FA and to alter the structure of FA into less toxic compounds.None of the bacterial strains were able to chemically modify FA. Highly FA resistant strains were found only in Gram-negative bacteria, mainly in the genus of Pseudomonas. The FA resistance of the Gram-negative bacteria was positively correlated with the number of predicted genes for FA efflux pumps present in the genome. Phylogenetic analysis of predicted FA resistance proteins (FUSC, an inner membrane transporter component of the efflux pump) revealed that FUSC proteins having high sequence identities with the functionally characterized FA resistance protein FusC or Fdt might be the major contributors of FA resistance. In contrast, most fungi converted FA to less toxic compounds regardless of the level of FA resistance they exhibited. Five derivatives were detected, and the detoxification of FA involved either oxidative reactions on the butyl side chain or reductive reactions on the carboxylic acid group. The production of these metabolites from widely different phyla indicates that resistance to FA by altering its structure is highly conserved. A few FA resistant saprophytic or biocontrol strains of fungi were incapable of altering FA, indicating a possible involvement of efflux transporters. Deployment of both efflux and derivatization mechanisms may be a common feature of fungal FA resistance

Desoxyhemigossypol 6-methyl ether

The title sesquiterpene [systematic name: 6-methoxy-10-methyl-7-(propan-2-yl)-2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4,6,8(12),9-pentaen-5-ol], C16H18O3, was isolated from pathogen-infected stele tissue of Gossypium barbadense. There are two molecules in the asymmetric unit and the dihedral angle between their naphthofuran systems is 86.48 (2)°. In the crystal, O—H...O hydrogen bonds between the hydroxy groups and etheric O atoms link the molecules into centrosymmetric tetramers. These tetramers are assembled into (010) layers via stacking interactions between the naphthofuran systems [interplanar distance 3.473 (3) Å] and short C—H...O contacts

Hemigossypol, a Constituent in Developing Glanded Cottonseed (Gossypium hirsutum)

Gossypol is a dimeric sesquiterpenoid first identified in cottonseed, but found in various tissues in the cotton plant including the seed. From its first discovery, it was assumed that hemigossypol was the biosynthetic precursor of gossypol. Previous studies established that peroxidase (either from horseradish or from cottonseed) converts hemigossypol to gossypol. However, hemigossypol has never been identified in healthy cottonseed. In a temporal study using HPLC and LC-MS, hemigossypol was identified in the developing cotton embryo. It was shown to concomitantly accumulate until 40 days postanthesis (dpa) with gossypol and with transcripts of δ-cadinene synthase and 8-hydroxy-δ-cadinene synthase, genes involved in the biosynthesis of hemigossypol and gossypol. After 40 dpa, hemigossypol and its biosynthetic gene transcript levels declined, whereas the gossypol level remained almost unchanged until the bolls were open. These results provide further evidence to support the previous findings that establish hemigossypol as the biosynthetic precursor of gossypol

Additional file 2: Table S9. of Genome-wide comparative analysis of NBS-encoding genes in four Gossypium species

Exon statistics in NBS genes and each NBS gene type in the four cotton species. (XLSX 9 kb

Additional file 6: Table S4. of Genome-wide comparative analysis of NBS-encoding genes in four Gossypium species

The amino acid sequence similarity between G. raimondii NBS genes and G. hirsutum NBS genes. (XLS 2569 kb