Hopanoids Again (and Again)

by Elio

What is stranger, the fact that hopanoids are pos­si­bly the most abun­dant or­ganic com­pounds on the planet or that, de­spite be­ing of mi­cro­bial ori­gin, most micro­bio­lo­gists have barely heard of them? Just as in­ex­plic­a­ble is that a PubMed search for "hopanoid" brings up a pal­try to­tal of 102 en­tries ("DNA" brings up 1,443,241 items!) To drive the point home, there are about 1012 tons of ho­panoids in the Earth's rocks (that's over 100 tons for eve­ry hu­man be­ing). No fault of STC Cen­tral: we have fea­tured hopanoids sev­eral times be­fore (here, here, and here).

Fig­ure 1. The struc­ture and the gener­alized syn­thetic path­ways of hopanoids and sterols. Source 

Let me re­cap. What are they? Hopanoids are cyclic mo­lecules that, like sterols, are de­rived from squa­lene but end up with an ex­tra ring (five) and an as­sort­ment of side chains that char­ac­ter­izes their many va­ri­eties. They are made by per­haps one in ten species of bac­te­ria and are con­stituents of their mem­branes, the cy­to­plas­mic in gram-pos­i­tives and prefer­entially the outer mem­brane in gram-neg­a­tives. Hopanoids are thought to act as mem­brane stiff­eners, which is what sterols do in eu­kary­otic mem­branes. This mat­ters to the cells be­cause when phos­pho­lipids are the lone lipids, at high tem­per­a­ture their mem­branes would be too fluid, im­pairing their growth and well-be­ing. In­deed, hopanoids are found promi­nently in ther­mophilic bac­te­ria. Ar­chaea do not seem to make hopanoids at all but some ther­mophilic ones solve their flu­id­ity prob­lem by mak­ing long bipo­lar lipids that span the mem­brane thick­ness.

In a re­cent study from the labs of ML Sum­mers and DK New­man, a ge­netic ap­proach firms up the con­clu­sion that hopanoids help rigid­ify mem­branes at high tem­per­a­tures. The au­thors made mu­tants of the fil­a­men­tous cyanobac­terium Nos­toc punc­ti­forme that are un­able to make any hopan­oids or are im­paired in methy­la­tion at the C‑2-po­si­tion. The mu­tant lack­ing hopanoids grows poor­ly at high tem­per­a­tures (where they are needed to stiffen the mem­brane) but bet­ter than the wild type at lower ones (where they over-rigid­ify the mem­brane). Oth­er­wise, veg­e­ta­tive growth at nor­mal growth tem­per­a­tures is not af­fected, in­di­cat­ing that hopanoids are ap­par­ently not needed other than un­der stress con­di­tions.

Both hopanoids and sterols are flat in shape, thus they can read­ily in­ter­ca­late in the lipid do­mains of mem­branes to rigid­ify them by negat­ing the ef­fect of the kinks in some of the phos­pho­lipids. How­ever, dif­fer­ent kinds of hopanoids do not be­have in the same way in mem­branes. Per­haps it is not sur­pris­ing that hopanoids can sub­sti­tute for sterols in the in­fre­quent bac­te­ria that re­quire ex­ternal sterols, such as My­coplasma my­coides. A study by Saenz et al. shows that hopanoids can in­deed act as the func­tional ana­logues of cho­les­terol.

Fig­ure 2. Hopanoids in­cor­po­rated into a lipid bi­layer. Source

Hopanoids are made at rel­a­tively low lev­els ex­cept when cells are stressed. In many cells grow­ing nor­mally, they com­prise 1–5% of the to­tal lipids but the fig­ure can rise to 50% in Zy­momonas, an al­co­hol-mak­ing and al­co­hol-re­­sis­tant bac­terium. A ther­mophile, Bacil­lus acidocal­darius, makes seven times more hopanoids at 65° C than at 60°C.

Be­sides be­ing made as a re­sponse to stress, hopanoid pro­duc­tion is as­so­ci­ated with spe­cific eco­log­i­cal niches. The ev­i­dence? A gene re­quired for the C‑2 hopanoid methy­lase, the en­zyme that makes of the spe­cific hopanoid 2‑methylhopanoid, is fre­quently found in or­gan­isms that are in­volved in plant-mi­crobe sym­bi­otic in­ter­ac­tions. In­ter­est­ing is that the gene is also found in bac­te­r­ial that are al­ways present in tightly packed mi­cro­bial biofilms, such as in stro­ma­to­lites, in hot spring sed­i­ments, and in hy­per­saline mi­cro­bial mats. Hopanoids are found in the actin­o­mycetes, bac­te­ria that of­ten make aer­ial fil­a­ments dur­ing the process of spore for­ma­tion. This aer­ial mode of life calls for spe­cial mem­brane prop­er­ties that may be re­lated to their hopanoid con­tent. More­over, hopanoids are made by Bacil­lus sub­tilis in the act of sporu­la­tion. The au­thors con­clude: "The com­mon fea­tures of these niches in­di­cate that 2‑methyl­hopanoids are en­riched in ses­sile mi­cro­bial com­mu­ni­ties in­hab­it­ing en­vi­ron­ments low in oxy­gen and fixed ni­tro­gen with high os­mo­lar­ity."

Fig­ure 3. Bac­te­r­ial lipids such as ho­panoids can act as bio­mark­ers when buried and pre­served in the se­di­mentary rock over bil­lions of years. Di­a­ge­n­e­sis refers to the chem­i­cal, phys­i­cal, or bio­logical changes that chan­ge sed­i­ments into rocks. Hopanoid mol­e­cules lose most of their func­tional groups but the ba­sic hopane struc­ture is pre­served over bil­lions of years. Geo­chemists are then able to ex­tract and de­tect these lipids in an­cient sed­i­ments. Source

The present study also sug­gest that hopanoids may be in­volved in stor­age of ni­tro­gen-con­tain­ing re­serve ma­terial. The cyanos they stud­ied (N. punc­ti­forme) make a spore-like rest­ing cell called the akinete. Here, hopanoids in the outer mem­brane are re­quired for tol­er­ance to stresses other than those re­sult­ing from high tempera­tures, e. g, treat­ment with the pep­ti­do­gly­can-de­grad­ing en­zyme lysozyme. Also, the hopanoid-de­fi­cient mu­tant does not ac­cu­mu­late in its akinetes gran­ules of an amino acid poly­mer called cyanophycin, which is used to store ni­tro­gen (and car­bon).

So, the story of what hopanoids do and when they are needed is a check­ered one in­deed. In fact, here is an­other sticky as­pect to it. The re­quire­ment for hopanoids in plant sym­bioses holds for Al­phapro­teobac­te­ria such as the rhi­zo­bia. It does not hold for the cyanobac­terium Nos­toc, where the hopanoid mu­tants do just fine dur­ing sym­bio­sis with the horn­wort An­tho­cerus punc­ta­tus. The gen­eral con­clu­sion is that hopanoids are bio­mark­ers for en­vi­ron­men­tal stresses. Just how they do this re­mains to be elu­ci­dated, prob­a­bly on a case-by-case ba­sis.

Now for the best part. Hopanoids don't much de­com­pose even across vastly long ge­o­logic times: some are 1.65 bil­lion years old! No won­der there is so much of the stuff. They are found in rocks and pe­tro­leum de­posits (chances are, you have them in the oil of your car's en­gine). Even if made in small amounts, ac­cu­mu­la­tion counts. I didn't find why hopanoids and, for that mat­ter, sterols, are so sta­ble to heat and pres­sure. I found a ref­er­ence to cho­les­terol be­ing sta­ble, but only over a pe­riod of three decades. The struc­ture of all these com­pounds looks com­pli­cated, which off­hand would make one think that they should be la­bile. But or­ganic chem­istry is what it is. Note that dur­ing the processes of rock for­ma­tion from sed­i­ments (di­a­ge­n­e­sis), some of the side chains of­ten get mod­i­fied or lost, leav­ing be­hind mainly the pen­ta­cyclic skele­tons (called the hopanes). How­ever, methyl groups at the C‑2 and C‑3 po­si­tion tend to be pre­served, a use­ful fact in pa­le­on­tol­ogy.

Given their longevity, hopanoids are im­por­tant bio­mark­ers for pa­le­on­to­log­i­cal stud­ies. They are "mol­e­c­u­lar fos­sils" that in­di­cate bac­te­r­ial ac­tiv­ity in the Ar­chaean pe­riod (that's an era, not to be con­fused with our friends, the ar­chaeal or­gan­isms). It was thought orig­i­nally that hopanoid syn­thesis re­quired oxy­gen, so it was sur­mised that some cyanobac­te­ria car­ried out oxy­genic photo­syn­thesis long be­fore oxy­gen be­came abun­dant in the at­mos­phere. How­ever, the non-oxy­genic pho­to­syn­the­sizer Rhodopseudomonas palus­tris makes such com­pounds anaer­o­bi­cally and in good amounts. Any­how, hopanoids are good stand-ins for bac­te­ria in fos­sils, just as sterols (or their degra­da­tion prod­ucts, the ster­anes) are for eu­kary­otes. Los­ing some of their side chain con­stituents makes find­ing them a bit murky. A most en­light­en­ing re­view on these sub­jects by New­man et al. was re­cently pub­lished.

Do hopanoids have uses, other than serv­ing as bio­mark­ers? Sur­pris­ingly, there are claims that some pen­ta­cyclic ter­penes, in­clud­ing hopanoids and non-hopanoids, have an­tipar­a­sitic prop­er­ties when ad­min­is­tered orally to lab­o­ra­tory an­i­mals. Af­fected are pro­to­zoa and ne­ma­todes. Per­haps they over-stiffen the mem­branes of these par­a­sites?

So there you have it, hopanoids are mol­e­cules that by any reck­on­ing are clearly out­ranked by the in­for­ma­tion mol­e­cules, and para­dox­i­cally dom­i­nate the chem­i­cal land­scape of this globe. One can wist­fully imag­ine what our sci­ence would be like if nu­cleic acids or pro­teins had such longevity. All it would take is a few sam­ples of bil­lion year-old DNA mol­e­cules to re­solve count­less ar­gu­ments about evo­lu­tion. Oh well, you can't win 'em all!

We re­cently dis­cussed the hopanoids in the pod­cast This Week in Mi­cro­bi­ol­ogy #134 ("Lipids That Live For­ever").
 

 

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