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Chondrus crispus (Rhodophycae) from Baker, A.L. et al.  2012.  Phycokey -- an image based key to Algae (PS Protista), Cyanobacteria, and other aquatic objects. University of New Hampshire Center for Freshwater Biology. 17 May 2014


Carrageenans form gels at low concentrations.


V Source
V Structural unit
V Molecular structure, κ-carrageenan, ι-carrageenan, λ-carrageenan, Helices
V Functionality


Carrageenan (E407) is a collective term for scaffolding polysaccharides prepared by alkaline extraction (and modification) from red seaweed (Rhodophycae) [1571], mostly of genus Chondrus, Eucheuma, Gigartina and Iridaea. Different seaweeds produce different carrageenans.

Structural unit

representative carrageenan structure

Carrageenan consists of alternating 3-linked-β-D-galactopyranose and 4-linked-α-D-galactopyranose units.

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Molecular structure

Carrageenans are linear polymers of about 25,000 galactose derivatives with regular but imprecise structures, dependent on the source and extraction conditions [292]. Idealized structures are given below and κ-carrageenan, for example, has been found to contain a small proportion of the dimer associated with ι-carrageenan.

κ-carrageenan (kappa-carrageenan) 



Alkaline conversion of mu- to kappa-carrageenan



κ-carrageenan is produced by alkaline elimination from μ-carrageenan [1623] isolated mostly from the tropical seaweed Kappaphycus alvarezii (also known as Eucheuma cottonii). The experimental charge/dimer is 1.03 rather than 1.0 with 0.82 molecules of anhydrogalactose rather than one.

ι-carrageenan (iota-carrageenan)



Alkaline conversion of nu- to iota-carrageenan



ι-carrageenan is produced by alkaline elimination from ν-carrageenan isolated mostly from the Philippines seaweed Eucheuma denticulatum (also called Spinosum). The experimental charge/dimer is 1.49 rather than 2.0 with 0.59 molecules of anhydrogalactose rather than one. The three-dimensional structure of the ι-carrageenan double helix has been determined [247] as forming a half-staggered, parallel, threefold, right-handed double helix, stabilized by interchain O2-H···O-5 and O6-H···O-2 hydrogen bonds between the β-D-galactopyranose-4-sulfate units (see structure). The structure of some calcium iota-carrageenans have been determined [1365]

λ-carrageenan (lambda-carrageenan)



Slow alkaline conversion of lambda- to theta-carrageenan



λ-carrageenan (isolated mainly from Gigartina pistillata or Chondrus crispus) is converted into θ-carrageenan (theta-carrageenan) by alkaline elimination, but at a much slower rate than causes the production of ι-carrageenan and κ-carrageenan. The experimental charge/dimer is 2.09 rather than 3.0 with 0.16 molecules of anhydrogalactose rather than zero.


The torsion angles phi (φH, H1C1OC4 or H1C1OC3), psi (ψH, C1OC4H4 or C1OC3C3) have been determined for λ-, μ- and ν-carrageenans [1095]. All carrageenans are highly flexible molecules which, at higher concentrations, wind around each other to form double-helical zones. Gel formation in κ- and ι-carrageenans involves helix formation on cooling from a hot solution together with gel-inducing and gel-strengthening K+ or Ca2+ cations respectively (not Na+, although Na+ does take part in an aggregation process to form weak gels with κ-carrageenan due to phase separation [723]), which not only aid helix formation but subsequently support aggregating linkages between the helices so forming the junction zones. The strongest gels of κ-carrageenan are formed with K+ rather than Li+, Na+, Mg2+, Ca2+, or Sr2+ [1077]. Incomplete formation of 1C4 3,6-anhydro-links will reduce the extent of helix formation as the unbridged α-linked galactose residues may flip to the 4C1 conformation.


κ-Carrageenan forms stronger gels in D2O rather than H2O. This has been attributed to an increase in the number of double-helix aggregates rather than the fraction of helix formed, which differs little between the two solvents [1670]. This is probably due to the increase in the affinity of D2O molecules for each other relative to polysaccharide water linkages..


Note that the gelling hydrocolloid agar is produced from the same family of seaweeds, the major difference being the presence of L- rather than D-3,6-anhydro-α-galactopyranose units but still forming double helical junction zones.  [Back to Top to top of page]


Carrageenans are used mainly for thickening, suspending and gelling. κ- and ι-carrageenans form thermoreversible gels on cooling in the presence of appropriate counter ions.  κ-Carrageenan forms a firm clear, if brittle, gel with poor freeze-thaw stability; the coil-double helix transition being followed by a K+-induced aggregation of the helices [516]. κ-Carrageenan gels may be softened (and is generally regarded to be synergistically strengtheneda) with locust bean gum. ι-Carrageenan has less specific ionic binding but increased ionic strength allows helices to form junction zones in soft elastic gels with good freeze-thaw stability. λ-Carrageenan is non gelling as the lack of the 1C4 3,6-anhydro-link allows the galactose residues to revert to their 4C1 conformation which does not allow the initial double helix formation required for gelling. Additionally, the high-density of charged sulfate groups encourages an extensive conformation. λ-Carrageenan has been found to act as a cryoprotectant and improves the freeze-thaw behavior of locust bean gum.


κ-Carrageenan stabilizes milk κ-casein products due to its charge interaction with the casein micelles (~200 nm diameter); their incorporation into the network preventing whey separation. Such complexes are soluble when both have same charge and are held together by counter ions or oppositely charged patches. Carrageenan is also used as a binder in cooked meats, to firm sausages and as a thickener in toothpaste and puddings.


It may be noted that a cancer health scare concerning degraded carrageenan has recently been examined by the European Commission Scientific Committee on Food which found no evidence in support and states that carrageenan is safe to use in foods. It is believed that carrageenan is safe to use in foods, within current regulations [1684].


Interactive structures are available (Jmol).  [Back to Top to top of page]


a However, a recent paper found no such synergy [290]. [Back]



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